Title of Invention | "IODOPHENYL-SUBSTITUTED CYCLIC KETOENOLS" |
---|---|
Abstract | The invention relates to novel iodophenyl-substituted cyclic ketenols of the formula (I)in which CKE, J, X and Y are as defined above, to a plurality of processes and intermediates for their preparation and to their use as pesticides and/or herbicides, and also to selective herbicidal ompositions comprising firstly iodophenyl-substituted cyclic of the formula (I) and secondly at least one crop plant compatibility-improving compound. |
Full Text | lodophenyl-sbsttted cyclic ketoenols The present nventon relates to novel odophenyl-sbsttted cyclc ketoenols, to a plralty ofprocesses for ther preparaton and for ther se as pestcdes and/or herbcdes. The nventon also provdes selectve herbcdal compostons comprsn8 frstly odophenyl-sbsttted cyclcketoenols and secondly a crop plant compatblty-mprovn8 compond. Pharmacetcal propertes of 3-acylpyrroldne-2,4-dones are descrbed n the pror art (S. Szk et al. Chem. Pharm. Bll. 5 20 (967)). Frthermore, R. Schmerer and H. Mldenber8er (Leb8s Ann. Chem. 985. 095) synthetzed N-phenylpyrroldne-2,4-dones. A bolo8cal actvty of these componds has not been descrbed. EP-A-0 262 399 and 8B-A-2 266 888 dsclose componds of a smlar strctre (3- arylpyrroldne-2,4-dones); however, a herbcdal, nsectcdal or acarcdal acton of these componds s not known. Known to have a herbcdal, nsectcdal or acarcdal acton are nsbsttted, bcyclc 3-arylpyrroldne-2,4-done dervatves (EP-A-355 599, EP-A-45 2 and -A-2-053 670), and also sbsttted monocyclc 3-arylpyrroldne-2,4-done dervatves (EP-A- 377 893 and EP-A-442 077). Also known are polycyclc 3-arylpyrroldne-2,4-done dervatves (EP-A-442 073), and also Harylpyrroldnedone dervatves (EP-A-456 063, EP-A-52 334, EP-A-596 298, EP-A-63 884, EP-A-63 885, WO 95/0 997, WO 95/26 954, WO 95/20 572, EP-A-0 668 267, WO 96/25 395, WO 96/35 664, WO 97/0 535, WO 97/02243, WO 97/36 868, WO 97/43275, WO 98/05638, WO 98/0672, WO 98/25928, WO 99/6748, WO 99/24437, WO 99/43649, WO 99/48869 and WO 99/55673, WO 0/7972, WO 0/23354, WO 0/74770, WO 03/03249, WO 04/007448, WO 04/024688, WO 04/065366, WO 04/080962, WO 04/042, WO 05/04479, WO 05/044796, WO 05/04870, WO 05/049596, DE-A-04 00 433. t s known that certan sbsttted A--dhydrofran-2-one dervatves have herbcdal propertes (cf. DE-A-4 04 420). The synthess of the tetronc acd dervatves (sch as, for example, 3methylphenyl)-4-hydroxy-5-(4-florophenyl)-A-'-dhydrofran-2-one) sed as startn8 materals s also descrbed n DE-A-4 04 420. Componds of a smlar strctre wth no stated nsectcdal and/or acarcdal actvty are known from the pblcaton Campbell et al., 2. Chem. Soc., Perkn Trans. , 985, (8) 567-76. Frthermore, 3-ary-A--dhydrofranone dervatves havn8 herbcdal, acarcdal and nsectcdal propertes are known from EP-A-528 56, EP-A-0 647 637, WO 95/26 345, WO 96/20 96, WO 96/25 395, WO 96/35 664, WO 97/0 535, WO 97/02 243, WO 97/36 868, WO 98/05638, WO 98/25928, WO 99/6748, WO 99/43649, WO 99/48869, 99/55673, WO 0/7972, WO 0/23354 and WO 0/74770, WO 03/03 249, WO 04/024 688, WO 04/080 962, WO 04/ 042. Also known are 3-aryl-A3-dhydrothphenone dervatves (WO 95/26345, 96/25395, WO 97/0535, WO 97/02243, WO 97/36868, WO 98/05638, WO 98/25928, WO 99/6748, WO 99/43649, WO 99/48869, WO 99/55673, WO 0/7972, WO 0/23354, WO 0/74770, WO 03/03249, WO 04/080 962, WO 04/ 042). Certan phenylpyrone dervatves nsbsttted n the phenyl rn8 are already known (cf. A.M. Chraz, T. Kappe and E. Ze8ler, Arch. Pharm. 309, 558 (976) and K.-H. Boltze and K. Hedenblth, Chem. Ber. 9, 2849); however, a possble se of these componds as pestcdes s not stated. Phenylpyrone dervatves whch are sbsttted n the phenyl rn8 and have herbcdal, acarcdal and nsectcdal propertes are descrbed n EP-A-588 37, WO 96/25 395, WO 96/35 664, WO 97/0 535, WO 97/02 243, WO 97/6 436, WO 97/9 94, WO 97/36 868, WO 98/05638, WO 99/43649, WO 99/48869, WO 99/55673, WO 0/7972, WO 0/74770, WO 03/03249, WO 04/080 962, WO 04/ 042. Certan 5-phenyl-l,3-thazne dervatves whch are nsbsttted n the phenyl rn8 are already known (cf. E. Ze8ler and E. Stener, Monatsh. 95, 47 (964), R. Ketcham, T. Kappe and E. Ze8ler, 2. Heterocycl. Chem. 0, 223 (973)); however, a possble se of these componds as pestcdes s not stated. 5-Phenyl-l,3-thazne dervatves whch are sbsttted n the phenyl rn8 and have herbcdal, acarcdal and nsectcdal acton are descrbed n WO 94/4 785, WO 96/02 539, WO 96/35 664, WO 97/0 535, WO 97/02 243, WO 97/02 243, WO 97/36 868, WO 99/05638, WO 99/43649, WO 99/48869, Wp 99/55673, WO 0/7972, WO 0/74770, WO 03/03249, WO 04/080 962, WO 04/ 042. t s known that certan sbsttted 2-arylcyclopentanedones have herbcdal, nsectcdal and acarcdal propertes (cf., for example, S-4 283 348; 4 338 22; 4 436 666; 4 526 723; 4 55 547; 4 632 698; WO 96/0 798; WO 96/03 366, WO 97/4 667 and also WO 98/3928, WO 99/43649, WO 99/48869, WO 99/55673, WO 0/7972, WO 0/74770, WO 03/03249, WO 04/080 962, WO 04/ 042). Also known are componds sbsttted n a smlar manner; 3-hydroxy-dmethyl-2-phenylcyclopent-2-ene-l-one from the pblcaton Mcklefeld et al., Tetrahedron, (992), 759-26 and the natral compond nvoltn (-)-cs-5-(3,4-dhydroxyphenyl)-3,4- dhydroxy-2-(4-hydroxypheny)cyclopent-2-enone from the pblcaton Edwards et al., 2. Chem. Soc. S, (967), 405-9. An nsectcdal or acarcdal acton s not descrbed. Also known s 2-(2,4,6- trmethylphenyl)-l,3-ndanedone from the pblcaton 2. Economc Entomolo8y, 66. (973), and the lad-open pblcaton DE-A 2 36 084, wth herbcdal and acarcdal actons ben8 stated. t s known that certan sbsttted 2-arylcyclohexanedones have herbcdal, nsectcdal and acarcdal propertes (S-4 75 35, 4209432, 4256657, 4256658, 4256659, 4257858, 4 283 348, 4 303 669, 4 35 666, 4 409 53, 4 436 666, 4 526 723, 4 63 67, 4 659 372, DE-A 2 83 34, and also Wheeler, T.N., 2. Or8. Chem. 44, 4906 (979)), WO 99/43649, WO 99/48869, WO 99/55673, WO 0/7972, WO 0/74770, WO 03/03249, WO 04/080 962, WO 04/ 042). t s known that certan sbsttted 4-arylpyrazoldne-3,5-dones have acarcdal, nsectcdal and herbcdal propertes (cf., for example, WO 92/650, EP-A-508 26, WO 96/574, WO 96/2 652, WO 99/47525, WO 0/735, WO 0/7 352, WO 0/7353, WO 0/7 972, WO 0/7 973, WO 03/028 466, WO 03/062 244, WO 04/080 962, WO 04/ 042, WO 05/005428, WO 05/06873). However, the effcacy and actvty spectrm of these componds, n partclar at low applcaton rates and concentratons, are not always satsfactory. Frthermore, the compatblty of these componds wth crops s not always sffcent. Ths nventon now provdes novel componds of the formla n whch 2 represents odne, X represents hydro8en, alkyl, halo8en, haloalkyl, alkoxy or haloalkoxy, Y represents hydro8en, alkyl, halo8en or alkoxy, wth the provso that at least one of the radcals 2, X or Y s located n the 2-poston of the phenyl radcal and s not hydro8en, A represents hydro8en, n each case optonally halo8en-sbsttted alkyl, alkenyl, alkoxyalkyl, alkylthoalkyl, satrated or nsatrated, optonally sbsttted cycloalkyl n whch optonally at least one rn8 atom s replaced by a heteroatom, or n each case optonally halo8en-, alkyl-, haloalkyl-, alkoxy-, haloalkoxy-, cyanoor ntro-sbsttted aryl, arylalkyl or hetaryl, B represents hydro8en, alkyl or alkoxyalkyl, or A and B to8ether wth the carbon atom to whch they are attached represent a satrated or nsatrated, nsbsttted or sbsttted cycle whch optonally contans at least one heteroatom, D represents hydro8en or an optonally sbsttted radcal from the 8rop consstn8 of alkyl, alkenyl, alkynyl, alkoxyalkyl, satrated or nsatrated cycloalkyl n whch optonally one or more rn8 members are replaced by heteroatoms, arylalkyl, aryl, hetarylalkyl or hetaryl or A and D to8ether wth the atoms to whch they are attached represent a satrated or nsatrated cycle whch s nsbsttted or sbsttted n the A,D moety and optonally contans at least one (n the case of CKE=8 one frther) heteroatom, or A and ' to8ether represent alkanedyl or alkenedyl, optonally sbsttted by hydroxyl, n each case optonally sbsttted alkyl, alkoxy, alkyltho, cycloalkyl, benzyloxy or aryl or ! represents hydro8en or alkyl, ndependently of one another represent hydro8en or alkyl, represents hydro8en, represents optonally sbsttted alkyl, alkoxyalkyl, alkylthoalkyl, optonally sbsttted cycloalkyl (n whch optonally one methylene 8rop s replaced by oxy8en or slfr) or optonally sbsttted phenyl, and to8ether wth the carbon atom to whch they are attached represent a satrated or nsatrated, nsbsttted or sbsttted cycle whch optonally contans a heteroatom, 8 represents hydro8en (a) or represents one of the 8rops E represents a metal on evalent or an ammonm on, L represents oxy8en or slfr, M represents oxy8en or slfr, R. represents n each case optonally halo8en-sbsttted alkyl, alkenyl, alkoxyalkyl, alylthoalkyl, polyalkoxyalkyl or optonally halo8en-, alkylor alkoxy-sbsttted cycloalkyl whch may be nterrpted by at least one heteroatom, n each case optonally sbsttted phenyl, phenylalkyl, hetaryl, phenoxyalkyl or hetaryloxyalkyl, R.2 represents n each case optonally halo8en-sbsttted alkyl, alkenyl, alkoxyalkyl, polyalkoxyalkyl or represents n each case optonally sbsttted cycloalkyl, phenyl or benzyl, R.3, R and R- ndependently of one another represent n each case optonally halo8en-sbsttted alkyl, alkoxy, alky lam no, dalkylamno, alkyltho, alkenyltho, cycloalkyltho or represent n each case optonally sbsttted phenyl, benzyl, phenoxy or phenyltho, R" and R' ndependently of one another represent hydro8en, n each case optonally halo8en-sbsttted alkyl, cycloalkyl, alkenyl, alkoxy, alkoxyalkyl, represent optonally sbsttted phenyl, represent optonally sbsttted benzyl, or to8ether wth the N atom to whch they are attached represent a cycle whch s optonally nterrpted by oxy8en or slfr. Dependn8 also on the natre of the sbsttents, the componds of the formla () can be present as 8eometrcal and/or optcal somers or somer mxtres of varyn8 composton whch, f approprate, may be separated n a cstomary manner. The present nventon provdes both the pre somers and the somer mxtres, ther preparaton and se, and compostons comprsn8 them. However, for the sake of smplcty, herenbelow only componds of the formla () are referred to, altho8h what s meant are both the pre componds and, f approprate, also mxtres havn8 varyn8 proportons of somerc componds. ) ncldn8 the meann8s () to (8) of 8rop CKE, the follown8 prncpal strctres (-) to A, B, D, 8, 2, , 2, 3, 4, 5, 6, X and Y are as defned above. ncldn8 the dfferent meann8s (a), (b), (c), (d), (e), (0 and (8) of 8rop 8, the follown8 prncpal strctres (-l-a) to (-l-8) reslt f CKE represents 8rop () (Figure Removed) A, B, E, 2, L, M, X, Y, R, R2, R3, R4, R5, R6 and R7 are as defned above. Dependn8 on the poston of the sbsttent 8, the componds of the formla (-4) can be present n the two somerc forms of the formlae (-4-A) and (-4-B) whch s meant to be ndcated by the dashed lne n the formla (-4). The componds of the formlae (-4-A) and (-4-B) can be present both as mxtres and n the form of ther pre somers. f approprate, mxtres of the componds of the formlae (-4-A) and (-4-B) can be separated n a manner known per se by physcal methods, for example by chromato8raphc methods. For reasons of clarty, herenbelow n each case only one of the possble somers s shown. Ths does not preclde that, f approprate, the componds may be present n the form of the somer mxtres or the respectve other somerc forms. ncldn8 the dfferent meann8s (a), (b), (c), (d), (e), (f) and (8) of 8rop 8, the follown8 prncpal strctres (-4-a) to (-4-8) reslt f CKE represents 8rop (4) (Figure Removed) A, D, E, 2, L, M, X, Y, R, R2, R3, R4, R5, R6 and R7 are as defned above. ncldn8 the dfferent meann8s (a), (b), (c), (d), (e), (f) and (8) of 8rop 8, the follown8 prncpal strctres (-5-a) to (-5-8) reslt f CKE represents 8rop (5) (Figure Removed)n whch A, E, 2, L, M, X, Y, R, R2, R3, R4, R5, R6 and R7 are as defned above. Dependn8 on the poston of the sbsttent 8, the componds of the formla (-6) can be present n the two somerc forms of the formlae (-6-A) and (-6-B) (Figure Removed) whch s meant to be ndcated by the dashed lne n the formla (). The componds of the formlae (-6-A) and (-6-B) can be present both as mxtres and n the form of ther pre somers. f approprate, mxtres of the componds of the formlae (-6-A) and (-6-B) can be separated by physcal methods, for example by chromato8raphc methods. For reasons of clarty, herenbelow n each case only one of the possble somers s shown. Ths does not preclde that, f approprate, the componds may be present n the form of the somer mxtres or the respectve other somerc forms. ncldn8 the dfferent meann8s (a), (b), (c), (d), (e), (f) and (8) of 8rop 8, the follown8 prncpal strctres (-6-a) to (-6-8) reslt: (Figure Removed) n whch A, B, 2, , 2, E, L, M, X, Y, R, R2, R3, R4, R5, R6 and R7 are as defned above. Dependn8 on the poston of the sbsttent 8, the componds of the formla (-7) can be present n the two somerc forms of the formlae (-7-A) and (-7-B), whch s meant to be ndcated by the dashed lne n the formla (-7): (-7-A) (-7-B) The componds of the formlae (-7-A) and (-7-B) can be present both as mxtres and n the form of ther pre somers. f approprate, mxtres of the componds of the formlae (-7-A) and (-7-B) can be separated by physcal methods, for example by chromato8raphc methods. For reasons of clarty, herenbelow n each case only one of the possble somers s shown. Ths does not preclde that, f approprate, the compond n eston may be present n the form of the somer mxtres or the respectve other somerc form. ncldn8 the dfferent meann8s (a), (b), (c), (d), (e), (f) and (8) of 8rop 8, the follown8 prncpal strctres (-7-a) to (-7-8) reslt: (Figure Removed) n whch A, B, 2, E, L, M, 3, 4, 5, 6, X, Y, R, R2, R3, R4, R5, R6 and R7 are as defned above. Dependn8 on the poston of the sbsttent 8, the componds of the formla (-8) can be present n the two somerc formlae (-8-A) and (-8-B) whch s meant to be ndcated by the dashed lne n the formla (-8). The componds of the formlae (-8-A) and (-8-B) can be present both as mxtres and n the form of ther pre somers. f approprate, mxtres of the componds of the formlae (-8-A) and (-8-B) can be separated n a manner known per se by physcal methods, for example by chromato8raphc methods. For reasons of clarty, herenbelow n each case only one of the possble somers s shown. Ths does not preclde that, f approprate, the componds may be present n the form of the somer mxtres or the respectve other somerc forms. ncldn8 the dfferent meann8s (a), (b), (c), (d), (e), (f) and (8) of 8rop 8, the follown8 prncpal strctres (-8-a) to (-8-8) reslt f Met represents the 8rop (8) (Figure Removed) n whch A, D, E, 2, L, M, X, Y, R, R2, R3, R4, R5, R6 and R7 are as defned above. Frthermore, t has been fond that the novel componds of the formla () are obtaned by one of the processes descrbed below: (A) sbsttted 3-phenylpyrroldne-2,4-dones or ther enols of the formla (-l-a) R.8 represents alkyl (preferably C2-C8-alkyl) are condensed ntramoleclarly n the presence of a dlent and n the presence of a base. (B) Frthermore, t has been fond that sbsttted 3-phenyl-4-hydroxy-A3-dhydrofranone dervatves of the formla (-2 -a) n whch A, B, 2, X , Y and R are as defned above are condensed ntramoleclarly n the presence of a dlent and n the presence of a base. (C) Frthermore, t has been fond that sbsttted 3-phenyl-4-hydroxy-A-- dhydrothophenone dervatves of the formla (-3-a) A, B, 2, X and Y are as defned above are obtaned when B-ketocarboxylc esters of the formla (V) A, B, 2, X, Y and R are as defned above and V represents hydro8en, halo8en, alkyl (preferably -alkyl) or alkoxy (preferably C2-C8-alkoxy) are cyclzed ntramoleclarly, f approprate n the presence of a dlent and n the presence of an acd. (D) Frthermore, t has been fond that the novel sbsttted 3-phenylpyrone dervatves of the 2, X and Y are as defned above and Hal represents halo8en (preferably chlorne or bromne), f approprate n the presence of a dlent and f approprate n the presence of an acd acceptor. Frthermore, t has been fond (E) that the novel sbsttted phenyl-l ,3-thazne dervatves of the formla (-5-a) A, 2, X and Y are as defned above are obtaned when thoamdes of the formla (V) H2N-C-A n whch A s as defned above are reacted wth ketene acd haldes of the formla (V) n whch Hal, 2, X and Y are as defned above, f approprate n the presence of a dlent and f approprate n the presence of an acd acceptor. Frthermore, t has been fond (F) that componds of the formla (-6-a) A, B, , 2, 2, X and Y are as defned above are obtaned when ketocarboxylc esters of the formla (V) A, B, l, 2, 2, X and Y are as defned above and R.8 represents alkyl (n partclar of a dlent and n the 6-aryl-5-ketohexanoc esters of the formla (X) are condensed ntramoleclarly n the presence of a dlent and n the presence of a base. (H) Frthermore, t has been fond that the componds of the formla (-8-a) Hal, X, Y and 2 are as defned above, f approprate n the presence of a dlent and f approprate n the presence of an acd acceptor, or 6) are reacted wth componds of the formla (X) n whch 2, X and Y are as defned above and represents NH2 or O-R8, where R8 s as defned above, f approprate n the presence of a dlent and f approprate n the presence of a base, or y) are reacted wth componds of the formla (X) (Figure Removed) A, D, 2, X, Y and R are as defned above, f approprate n the presence of a dlent and f approprate n the presence of a base. Moreover, t has been fond () that the componds of the formlae (-l-b) to (-8-b) shown above n whch A, B, D, 2, , R', X and Y are as defned above are obtaned when componds of the formlae (-l-a) to (-8-a) shown above n whch A, B, D, 2, , 2, 3, 4, 5, 6, X and Y are as defned above are n each case (a) reacted wth acd haldes of the formla (X) n whch R! s as defned above and Hal represents halo8en (n partclar chlorne or bromne) or (B) wth carboxylc anhydrdes of the formla (XFV) f approprate n the presence of a dlent and f approprate n the presence of an acd bnder; (2) that the componds of the formlae (-l-c) to (-8-c) shown above n whch A, B, D, 2, , R M. X and Y are as defned above and L represents oxy8en are obtaned when componds of the formlae (-l-a) to (-8-a) shown above n whch A, B, D 2, l, , , 4; 55 65 x and Y are as defned above are n each case reacted wth chloroformc esters or chloroformc thoesters of the formla (XV) R.2 and M are as defned above f approprate n the presence of a dlent and f approprate n the presence of an acd bnder; (K) that componds of the formlae (-l-c) to (-8-c) shown above n whch A, B, D, 2, , 2, R, M, X and Y are as defned above and L represents slfr are obtaned when componds of the formlae (-l-a) to (-8-a) shown above n whch A, B, D, 2, , X and Y are as defned above are n each case reacted wth chloromonothoformc esters or chlorodthoformc esters of the formla (Figure Removed) M and R2 are as defned above, f approprate n the presence of a dlent and f approprate n the presence of an acd bnder, and (Figure Removed) the formlae (-l-a) to (-8-a) shown above n whch A, B, D, 2, , 2, 3, 4, 5, 6, X and Y are as defned above are n each case reacted wth slfonyl chlordes of the formla (XV) R3-SO2-C (XV) n whch R3 s as defned above, f approprate n the presence of a dlent and f approprate n the presence of an acd bnder, (M) that componds of the formlae (-l-e) to (-8-e) shown above n whch A, B, D, 2, L, Cr, X and Y are as defned above are obtaned when componds of the formlae (-l-a) to (-8-a) shown above n whch A, B, D, 2, , 2, 3, 4, 5, , X and Y are as defned above are n each case reacted wth phosphors componds of the formla (XV) L, R4 and R are as defned above and Hal represents halo8en (n partclar chlorne or bromne), f approprate n the presence of a dlent and f approprate n the presence of an acd bnder, (N) that componds of the formlae (-l-f) to (-8-f) shown above n whch A, B, D, E, 2, l, , X and Y are as defned above are obtaned when componds of the formlae (-l-a) to (-8-a) n whch A, B, D, 2, , 2, 3, 4, 5, 6, X and Y are as defned above are n each case reacted wth metal componds or amnes of the formlae (XX) or (XX) Me represents a mono- or dvalent metal (preferably an alkal metal or alkalne earth metal, sch as lthm, sodm, potassm, ma8nesm or calcm), or represents an ammonm on t represents the nmber or 2 and RlO, R., R2 ndependently of one another represent hydro8en or alkyl (preferably C2- f approprate n the presence of a dlent, (O) that componds of the formlae (-l-8) to (-8-8) shown above n whch A, B, D, 2, L, , 2, 3, 4, 5; 6; R R?; x and Y are as defned above are obtaned when componds of the formlae (-l-a) to (-8-a) shown above n whch A, B, D, 2, , 2, 3, 4, 5, ", X and Y are as defned above are n each case (a) reacted wth socyanates or sothocyanates of the formla (XX) f approprate n the presence of a dlent and f approprate n the presence of a catalyst, reacted wth carbamoyl chlordes or thocarbamoyl chlordes of the formla (XX) R (Figure Removed) n whch L, R.6 and R7 are as defned above, f approprate n the presence of a dlent and f approprate n the presence of an acd bnder, that componds of the formlae (-l-a) to (-8-a) shown above n whch A, B, D, 2, , 2, 3 4, 5) 6, X and Y are as defned above are obtaned when componds of the formlae (-l-a) to (-8-a) n whch A, B, D, , 2, 3, 4, 5, 6, X and Y are as defned above and W preferably represents bromne a) are reacted wth metal oddes (for example sodm odde or potassm odde), f approprate n the presence of a dlent, a C() salt (for example CBr, Cl) and a base (for example N,N-dmethylethylenedamne), or 6) sb2ected to a halo8en/metal exchan8e wth metal or8anyls (for example n, s-, -btyllthm) and the anon formed s enched wth odnatn8 a8ents (for example odne, odne monochlorde). Frthermore, t has been fond that the novel componds of the formla () have 8ood actvty as pestcdes, preferably as nsectcdes, acarcdes and/or herbcdes. Srprsn8ly, t has now also been fond that certan sbsttted cyclc ketoenols, when employed to8ether wth the crop plant compatblty-mprovn8 componds (safeners/antdotes) descrbed later on, are extremely 8ood at preventn8 dama8e to the crop plants and can be sed wth partclar advanta8e as broad-spectrm combnaton prodcts for the selectve control of nwanted plants n crops of sefl plants, sch as, for example, n cereals, bt also n corn, soya beans and rce. The nventon also provdes selectve herbcdal compostons comprsn8 an effectve amont of an actve compond combnaton comprsn8, as components, (a) at least one sbsttted cyclc ketoenol of the formla () n whch CKE, 2, X and Y are defned above and (b') at least one crop plant compatblty-mprovn8 compond from the follown8 8rop of componds: 4-dchloroacetyl-l-oxa-4-azaspro[4.5]decane (AD-67, MON-4660), -dchloroacetylhexahydro- 3,3,8a-trmethylpyrrolo[l,2-a]pyrmdn-6(2H)-one (dcyclonon, BAS-4538), 4-dchloroacetyl- 3,4-dhydro-3-methy!-2H-l,4-benzoxa/ne (benoxacor), -methylhexyl 5-chloronolne-8-oxyacetate (clontocet-mexyl - cf. also related componds n EP-A-86750, EP-A-94349, EP-A-9736, EP-A-492366), 3-(2-chlorobenzyl)-l-(l-methyl-l-phenylethyl)rea (cmylron), a-(cyanomethoxmno)phenylacetontrle (cyometrnl), 2,4-dchlorophenoxyacetc acd (2,4-D), 4-(2,4-dchlorophenoxy)btyrc acd (2,4-DB), l-(l-methyl-l-phenylethyl)-3-(4-methylphenyl)rea (damron, dymron), 3,6-dchloro-2-methoxybenzoc acd (dcamba), S-l-methyl--phenylethyl pperdne--thocarboxylate (dmepperate), 2,2-dchloro-N-(2-oxo-2-(2-propenylamno)ethyl)- N-(2-propenyl)acetamde (DKA-24), 2,2-dchloro-N,N-d-2-propenylacetamde (dchlormd), 4,6-dchloro-2-phenylpyrmdne (fenclorm), ethyl l-(2,4-dchlorophenyl)-5-trchloromethyl- lH-l,2,4-trazole-3-carboxylate (fenchlorazole-ethyl - cf. also related componds n EP-A-74562 and EP-A-346620), phenylmethyl 2-chloro-4-trfloromethylthazole-5-carboxylate (flrazole), 4-chloro-N-(l,3-doxolan-2-ylmethoxy)-a-trfloroacetophenone oxme (flxofenm), 3-dchloroacetyl- 5-(2-franyl)-2,2-dmethyloxazoldne (frlazole, MON-3900), ethyl 4,5-dhydro- 5,5-dphenyl-3-soxazolecarboxylate (soxadfen-ethyl - cf. also related componds n WO-A-95/07897), l-(ethoxycarbonyl)ethyl 3,6-dchloro-2-methoxybenzoate (lactdchlor), (4-chloro-o-tolyloxy)acetc acd (MCPA), 2-(4-chloro-o-tolyloxy)proponc acd (mecoprop), dethyl l-(2,4-dchorophenyl)-4,5-dhydro-5-methyl-lH-pyrazole-3,5-dcarboxylate (mefenpyrdethyl - cf. also related componds n WO-A-9/07874), 2-dchloromethyl-2-methyl-l,3- doxolane (M8-9), 2-propenyl-l-oxa-4-azaspro[4.5]decane-4-carbodthoate (M8-838), ,8-naphthalc anhydrde, a-(l,3-doxolan-2-ylmethoxmno)phenylacetontrle (oxabetrnl), 2,2-dchloro-N-(l,3-doxolan-2-ylmethyl)-N-(2-propenyl)acetamde (PP8-292), 3-dchloroacetyl- 2,2-dmethyloxazoldne (R-28725), 3-dchloroacetyl-2,2,5-trmethyloxazoldne (R-2948), 4-(4- chloro-o-tolyl)btyrc acd, 4-(4-chlorophenoxy)btyrc acd, dphenylmethoxyacetc acd, methyl dphenylmethoxyacetate, ethyl dphenylmethoxyacetate, methyl l-(2-chlorophenyl)-5-phenyllH- pyrazole-3-carboxylate, ethyl l-(2,4-dchlorophenyl)-5-methyl-lH-pyrazole-3-carboxylate, ethyl l-(2,4-dchlorophenyl)-5-sopropyl-lH-pyrazole-3-carboxylate, ethyl l-(2,4-dchlorophenyl)- 5-(l,l-dmethylethyl)-lH-pyrazole-3-carboxylate, ethyl l-(2,4-dchlorophenyl)-5-phenyllH- pyrazole-3-carboxylate (cf. also related componds n EP-A-269806 and EP-A-3333), ethyl 5-(2,4-dchlorobenzyl)-2-soxazolne-3-cafboxylate, ethyl 5-phenyl-2-soxazolne-3-carboxylate, ethyl 5-(4-florophenyl)-5-phenyl-2-soxazolne-3-carboxylate (cf. also related componds n WO-A-9/08202), ,3-dmethylbt-l-y 5-chloronolne-8-oxyacetate, 4-allyloxybtyl 5-chloronolne- 8-oxyacetate, l-allyloxyprop-2-yl 5-chloronolne-8-oxyacetate, methyl 5-chloronoxalne-8-oxyacetate, ethyl 5-chloronolne-8-oxyacetate, allyl 5-chloronoxalne- 8-oxyacetate, 2-oxoprop-l-yl 5-chloronolne-8-oxyacetate, dethyl 5-chloronolne- 8-oxymalonate, dallyl 5-chloronoxalne-8-oxymalonate, dethyl 5-chloronolne-8-oxymalonate (cf. also related componds n EP-A-58298), 4-carboxychroman-4-ylacetc acd (AC-30445, cf. EP-A-6368), 4-chlorophenoxyacetc acd, 3,3'-dmethyl-4-methoxybenzophenone, -bromo-4-chloromethylslfonylbenzene, -[4-(N-2-methoxybenzoylslfamoyl)- phenyl]-3-methylrea (also known as N-(2-methoxybenzoyl)-4-[(rnethylamnocarbonyl)- amno]benzeneslfonamde), l-[4-(N-2-methoxybenzoylslfamoyl)phenyl]-3,3-dmethylrea, l-[4- (N-4,5-dmethylbenzoylslfamoyl)phenyl]-3-methylrea, l-[4-(N-naphthylslfamoyl)phenyl]-3,3- dmethylrea, N-(2-methoxy-5-methylbenzoyl)-4-(cyclopropylamnocarbonyl)- benzeneslfonamde, and/or one of the follown8 componds, defned by 8eneral formlae, of the 8eneral formla (Ha) n represents a nmber 0, , 2, 3, 4 or 5, A2 represents optonally C|-C4-alky- and/or C-C4-alkoxy-carbonyl- and/or C-C4-alkenyloxycarbonyl- sbsttted alkanedyl havn8 or 2 carbon atoms, R4 represents hydroxyl, mercapto, amno, C-C6-alkoxy, -C6-alkyltho, CrC6-alkylamno or d(CrC4-alkyl)-amno, R.'5 represents hydroxyl, mercapto, amno, CrC7-alkoxy, C-C6-alkenyloxy, C-C6-alkenyloxy-C,- C6-alkoxy, CrC6-alkyltho, CrCe-alkylamno or d(C-C4-alkyl)-amno, R6 represents n each case optonally florne-, chlorne- and/or bromne-sbsttted CrC4-alkyl, R7 represents hydro8en, n each case optonally florne-, chlorne- and/or bromne-sbsttted C|-C6-alkyl, C2-C6-alkenyl or C2-C6-alkynyl, C,-C4-alkoxy-C-C4-alkyl, doxolanyl-CrC4- alkyl, fryl, fryl-CrC4-alkyl, thenyl, thazolyl, pperdnyl, or optonally florne-, chlorneand/ or bromne- or C-C4-alkyl-sbsttted phenyl, R8 represents hydro8en, n each case optonally florne-, chlorne- and/or bromne-sbsttted CrC6-alkyl, C2-C6-alkenyl or C2-C6-alkynyl, C,-C4-alkoxy-C,-C4-alkyl, doxolanyl-C,-C4- alkyl, fryl, fryl-C|-C4-alkyl, thenyl, thazolyl, pperdnyl, or optonally florne-, chlorneand/ or bromne- or CrC4-alkyl-sbsttted phenyl, R7 and R8 also to8ether represent C3-C6-alkanedyl or C2-C5-oxaalkanedyl, each of whch s optonally sbsttted by C|-C4-alkyl, phenyl, fryl, a fsed benzene rn8 or by two sbsttents whch, to8ether wth the C atom to whch they are attached, form a 5- or 6- membered carbocycle, R9 represents hydro8en, cyano, halo8en, or represents n each case optonally florne-, chlorneand/ or bromne-sbsttted C,-C4-alkyl, C3-C6-cycloalkyl or phenyl, R20 represents hydro8en, optonally hydroxyl-, cyano-, halo8en- or CrC4-alkoxy-sbsttted C6- alkyl, C3-C6-cycloalkyl or tr-(CrC4-alkyl)-slyl, R2 represents hydro8en, cyano, halo8en, or represents n each case optonally florne-, chlorneand/ or bromne-sbsttted -C4-alkyl, C3-C6-cycloalkyl or phenyl, X represents ntro, cyano, halo8en, C|-C4-alkyl, CrC4-raloalkyl, CrC4-alkoxy or CrC4- haloalkoxy, X2 represents hydro8en, cyano, ntro, halo8en, C-C4-alkyl, C-C4-haloalkyl, -C4-alkoxy or C\- C4-haloalkoxy, X3 represents hydro8en, cyano, ntro, halo8en, -C4-alkyl, CrC4-haloalkyl, CrC4-alkoxy or C- C4-haloalkoxy, and/or the follown8 componds, defned by 8eneral formlae, of the 8eneral formla (ld) Preferred sbsttents or ran8es of the radcals lsted n the formlae 8ven above and below are llstrated below: 2 preferably represents odne, X preferably represents hydro8en, halo8en, -alkyl, C-C,4-haloalkyl, C2-C8-alkoxy or Y preferably represents hydro8en, C2-C8-alkyl, halo8en or C 2 -C8-alkoxy, wth the provso that at least one of the radcals 2, X or Y s located n the 2-poston of the phenyl radcal and s not hydro8en, CKE preferably represents one of the 8rops A preferably represents hydro8en or n each case optonally halo8en-sbsttted C alkyl, C3-C8-alkenyl, C-C-alkoxy-CC8-alkyl, C-C-alkyltho-C2-C8-alkyl, optonally halo8en-, C2-C8-alkyl- or -C6-alkoxy-sbsttted C3-C8-cycloalkyl n whch optonally one or two not drectly ad2acent rn8 members are replaced by oxy8en and/or slfr or represents n each case optonally halo8en-, C2-C8-alkyl-, C2-C8-haloalkyl-, C2- C8-alkoxy-, C2-C8-haloalkoxy-, cyano- or ntro-sbsttted phenyl, naphthyl, hetaryl havn8 5 to 6 rn8 atoms (for example franyl, pyrdyl, mdazolyl, trazolyl, pyrazolyl, pyrmdyl, thazolyl or thenyl), phenyl-C-C8-alkyl or naphthyl-C2-C8-alkyl, B preferably represents hydro8en, C2-C-alkyl or C2-C8-alkoxy-C2-C8-alkyl, or A, B and the carbon atom to whch they are attached preferably represent satrated C3-C2ocycloalkyl or nsatrated Cf-C2o-cycloalkyl n whch optonally one rn8 member s replaced by oxy8en or slfr and whch are optonally mono- or dsbsttted by C2-C8alkyl, C3-Co-cyc'°alkyl, C2-C8-haloalkyl, C2-C8-alkoxy, C2-C4-alkoxy-C-C4-alkoxy, C2-C8-alkyltho, halo8en or phenyl or A, B and the carbon atom to whch they are attached preferably represent C3-C8-cycloalkyl whch s sbsttted by an alkylenedthoyl 8rop or by an alkylenedoxyl 8rop or by an alkylenedyl 8rop whch optonally contans one or two not drectly ad2acent oxy8en and/or slfr atoms and whch s optonally sbsttted by -C4-alkyl, whch 8rop, to8ether wth the carbon atom to whch t s attached, forms a frther fve- to e8htmembered rn8, or A, B and the carbon atom to whch they are attached preferably represent C3-C8-cycloalkyl or (Fi8re Removed) whch optonally one rn8 member s replaced by oxy8en or slfr, 8 preferably represents hydro8en (a) or represents one of the 8rops E represents a metal on evalent or an ammonm on, L represents oxy8en or slfr and M represents oxy8en or slfr. R. preferably represents n each case optonally halo8en-sbsttted C-C2-alkyl, C2-C2alkenyl, C-C8-alkoxy-C-C8-alkyl, C-C8-alkyltho-C-C8-alkyl, poly-C2-C8-alkoxy- C2-C8-alkyl or optonally halo8en-, C2-C8-alkyl- or C2-C8-alkoxy-sbsttted C3-C8cycloalkyl n whch optonally one or more (preferably not more than two) not drectly ad2acent rn8 members are replaced by oxy8en and/or slfr, preferably represents optonally halo8en-, cyano-, ntro-, C2-C8-alkyl-, C \ -C8-alkoxy-, C2-C5-haloalkyl-, C2-C8-haloalkoxy-, C2-C8-alkyltho- or C-C8-alkylslfonylsbsttted preferably represents optonally halo8en-, ntro-, cyano-, C2-C8-alkyl-, C2-C8-alkoxy-, C2-C8-haloalkyl- or C2-C8-haloalkoxy-sbsttted phenyl-C2-C8-alkyl, preferably represents optonally halo8en- or C2-C8-alkyl-sbsttted 5- or 6-membered hetaryl (for example pyrazolyl, thazolyl, pyrdyl, pyrmdyl, franyl or thenyl), preferably represents optonally halo8en- or C2-C8-alkyl-sbsttted phenoxy-C2-C8-alkyl optonally halo8en-, amno- or C2-C8-alkyl-sbsttted 5- or 6- membered hetaryloxy--C8-alkyl (for example pyrdyloxy-C2-C8-alkyl, pyrmdyloxy- C -C8-alkyl or thazolyloxy-C 2 -C8-alkyl), R preferably represents n each case optonally halo8en-sbsttted -C2-alkyl, C2-C2alkenyl, C 2 -C8-alkoxy-C2-C8-alky , poly-C 2 -C8-alkoxy-C2-C8-alkyl, preferably represents optonally halo8en-, C2-C8-alkyl- or C\-C6-alkoxy-sbsttted €3- C8-cycloalkyl or preferably represents n each case optonally halo8en-, cyano-, ntro-, C2-C5-alkyl-, C2- C8-alkoxy-, C2-C8-haloalkyl- or C2-C8-haloalkoxy-sbsttted phenyl or benzyl, -43- R.3 preferably represents optonally halo8en-sbsttted C2-C8-alkyl or represents n each case optonally halo8en-, C2-C8-alkyl-, C2-C8-alkoxy-, C2-Chaloalkyl-, C2-C4-haloalkoxy-, cyano- or ntro-sbsttted phenyl or benzyl, R.4 and Rr ndependently of one another preferably represent n each case optonally halo8ensbsttted C2-C8-alkyl, C2-C8-alkoxy, C2-C8-alkylamno, d-(C2-C8-alkyl)amno, C2- C8-alkyltho, C2-C8-alkenyltho, C3-C7-cycloalkyltho or represent n each case optonally halo8en-, ntro-, cyano-, C 2 -C4-alkoxy-, C 2 -C4-haloalkoxy-, C-C4-alkyltho-, -C4- haloalkyltho-, C-C4-alkyl- or -C4-haloalkyl-sbsttted phenyl, phenoxy or phenyltho, R" and R ndependently of one another preferably represent hydro8en, represent n each case optonally halo8en-sbsttted C2-C8-alkyl, C3-C8-cycloalkyl, C2-C8-alkoxy, C3~C8alkenyl, C2-C8-alkoxy-C-C8-alkyl, represent optonally halo8en-, C2-C8-haloalkyl-, C2- C8-alkyl- or C2-C8-alkoxy-sbsttted phenyl, optonally halo8en-, C2-C8-alkyl-, C2-C8haloalkyl- or C|-C8-alkoxy-sbsttted benzyl or to8ether represent an optonally C2-C4- alkyl-sbsttted C3-C5-alkylene radcal n whch optonally one carbon atom s replaced by oxy8en or slfr, Rl3 preferably represents hydro8en, preferably represents n each case optonally halo8ensbsttted C2-C8-alkyl or -C8-alkoxy, preferably represents optonally halo8en-, C2- C4-alky- or C2-C4-alkoxy-sbsttted C3-C8-cycloalkyl n whch optonally one methylene 8rop s replaced by oxy8en or slfr, or preferably represents n each case optonally halo8en-, C2-C8-alkyl-, C2-C8-alkoxy-, C2-haloalkyl-, C2-haloalkoxy-, ntro- or cyano-sbsttted phenyl, phenyl-C-C4-alkyl or phenyl--C4-alkoxy, Rl4a preferably represents hydro8en or C2-C8-alkyl, or and Ra to8ether preferably represent C4-C8-alkanedyl, and Ra are dentcal or dfferent and preferably represent C2-C5-alkyl, or anc2 Rl6a to8ether preferably represent a C2~C4-alkanedyl radcal whch s optonally sbsttted by C-C8-alkyl, C-C8-haloalkyl or by optonally halo8en-, C2-C8-alkyl-, C2- C4-haloalkyl-, C2-C8-alkoxy-, C 2 -C4-haloalkoxy-, ntro- or cyano-sbsttted phenyl, and R a ndependently of one another preferably represent hydro8en, represent optonally halo8en-sbsttted C2-C8-alky or represent optonally halo8en-, -C6-alkyl-, C2-C8alkoxy-, C2-C4-haloalkyl-, -C4-haloalkoxy-, ntro- or cyano-sbsttted phenyl, or -44- and R8a to8ether wth the carbon atom to whch they are attached preferably represent a carbonyl 8rop or represent optonally halo8en-, C2-Calkyl- or C2-Calkoxy-sbsttted C5-C7-cycloalkyl n whch optonally one methylene 8rop s replaced by oxy8en or slfr, and R20a ndependently of one another preferably represent C2-C-alkyl, C2-o-alkenyl, C-C2-alkoxy, C-C2-alkylamno, C3--alkenylamno, d-(C-C2o-alkyl)amno or d-(C3-C2o-alkenyl)amno. n the radcal defntons mentoned as ben8 preferred, halo8en represents florne, chlorne, bromne and odne, and n partclar florne, chlorne and bromne. 2 partclarly preferably represents odne, X partclarly preferably represents hydro8en, florne, chlorne, bromne, odne, C2-C alkyl, trfloromethyl, C2-Calkoxy, dfloromethoxy or trfloromethoxy, Y partclarly preferably represents hydro8en, florne, chlorne, bromne, odne, C\-C- alkyl or C2-Calkoxy, wth the provso that at least one of the radcals 2, X or Y s located n the 2-poston of the phenyl radcal and s not hydro8en. Here, the radcals 2, X and Y, havn8 ther partclarly preferred meann8s, are partclarly preferably present n the follown8 phenyl sbsttton patterns (Figre Removed) where only n the phenyl sbsttton patterns (A) and (8) X may also represent hydro8en. CKE partclarly preferably represents one of the 8rops A partclarly preferably represents hydro8en, represents C-C8-alky! or C-C C2-alkyl, each of whch s optonally mono- to trsbsttted by florne or chlorne, represents C3-C8-cycloalkyl whch s optonally mono- to dsbsttted by C2-C2-alkyl or -C2-alkoxy or (bt not n the case of the componds of the formlae (-3), (-4), (-6) and (-7)) represents phenyl or benzyl, each of whch s optonally mono- to dsbsttted by florne, chlorne, bromne, C2-Calkyl, C-C2-haloalkyl, C2-Calkoxy, -C2- haloalkoxy, cyano or ntro, B partclarly preferably represents hydro8en, C-C4-alkyl or C-C2-alkoxyl-C-C2-alkyl) or A, B and the carbon atom to whch they are attached partclarly preferably represent satrated or nsatrated C5-Cy-cycloalkyl n whch optonally one rn8 member s replaced by oxy8en or slfr and whch s optonally mono- to dsbsttted by -C6-alkyl, trfloromethyl, C2-C8-alkoxy or C2-C-alkoxy-C-alkoxy, wth the provso that n ths case Cr partclarly preferably represents hydro8en or methyl, or A, B and the carbon atom to whch they are attached partclarly preferably represent C5-C8cycloalkyl whch s sbsttted by an alkylenedthol 8rop or by an alkylenedoxyl 8rop or by an alkylenedyl 8rop whch optonally contans one or two not drectly ad2acent oxy8en or slfr atoms and whch s optonally sbsttted by methyl or ethyl, whch 8rop to8ether wth the carbon atom to whch t s attached forms a frther fve- or sx-membered rn8, wth the provso that n ths case partclarly preferably represents hydro8en or methyl, A, B and the carbon atom to whch they are attached partclarly preferably represent cycloalkyl or C5-C8-cycloalkenyl n whch two sbsttents to8ether wth the carbon atoms to whch they are attached represent n each case optonally C-C2-akyl- or -C2- alkoxy-sbsttted C2-C4-alkanedyl, C2-C4-alkenedyl or btadenedyl, wth the provso that -3 n ths case represents hydro8en or methyl, D partclarly preferably represents hydro8en, partclarly preferably represents C2-C8-alkyl, C3-C5-alkenyl, C-C4-alkoxy-C2~C3-alkyl, each of whch s optonally mono- to trsbsttted by florne, partclarly preferably represents C3-C8-cycloalkyl whch s optonally mono- to dsbsttted by C-C4-alkyl, C2-alkoxy or C-C2-haloalkyl and n whch optonally one methylene 8rop s replaced by oxy8en or (bt not n the case of the componds of the formlae (-)) represents phenyl or pyrdyl, each of whch s optonally mono- to dsbsttted by florne, chlorne, bromne, C2-C4-alkyl, C2-C4- haloalkyl, C2-C4-alkoxy or C2-haloalkoxy, or A and D to8ether partclarly preferably represent optonally mono- to dsbsttted €3-05- alkanedyl n whch one methylene 8rop may be replaced by a carbonyl 8rop (bt not n the case of the componds of the formla (-)), ox8en or slfr, possble sbsttents ben8 -C2-alkyl or C2-C2-alkoxy, or A and ' to8ether partclarly preferably represent C3-C4-alkanedyl whch s n each case optonally mono- or dsbsttted by dentcal or dfferent sbsttents selected from the 8rop consstn8 of C 2 -C2-alkyl and C \ -C2-alkoxy, or partclarly preferably represents hydro8en, 2 partclarly preferably represents hydro8en, Cr, - and " ndependently of one another partclarly preferably represent hydro8en or C2- -5 partclarly preferably represents hydro8en, C2-alkyl, or C3-C6-cycloalkyl whch s optonally mono- to dsbsttted by methyl or methoxy, or and to8ether wth the carbon to whch they are attached partclarly preferably represent an optonally C2-C2-alkyl- or C-C2-alkoxy-sbsttted satrated C5-C8-rn8 n whch optonally one rn8 member s replaced by oxy8en or slfr, wth the provso that n ths case A partclarly preferably represents hydro8en or methyl, 8 partclarly preferably represents hydro8en (a) or represents one of the 8rops E represents a metal on evalent or an ammonm on, L represents oxy8en or slfr and M represents oxy8en or slfr, R. partclarly preferably represents C2-C8-alkyl, C2-8-alkenyl, -C4-alkoxy--C2- alkyl, C-C4-alkyltho-C-C2-alkyl, each of whch s optonally mono- to trsbsttted florne or chlorne, or C3-C8-cycloalkyl whch s optonally mono- to dsbsttted by florne, chlorne, -C2-alkyl or -C2-alkoxy and n whch optonally one or two not drectly ad2acent rn8 members are replaced by oxy8en, partclarly preferably represents phenyl whch s optonally mono- to dsbsttted by florne, chlorne, bromne, cyano, ntro, -C4-alkyl, C 2 -C4-alkoxy, C2-C2-haloalkyl or C2-C2-haloalkoxy, -49- , R2 partclarly preferably represents C2-C8-alkyl, C2-C8-alkenyl or C2-C alkyl, each of whch s optonally mono- to trsbsttted by florne, partclarly preferably represents C3-C8-cycloalkyl whch s optonally monosbsttted by C2-C2-alkyl or C2-C2-alkoxy or partclarly preferably represents phenyl or benzyl, each of whch s optonally mono- to dsbsttted by florne, chlorne, bromne, cyano, ntro, C-Calkyl, C2-alkoxy, trfloromethyl or trfloromethoxy, R.3 partclarly preferably represents C2-C8-alkyl whch s optonally mono- to trsbsttted by florne or represents phenyl whch s optonally monosbsttted by florne, chlorne, bromne, C2-Chalky , C2-Calkoxy, trfloromethyl, trfloromethoxy, cyano or ntro, R.4 partclarly preferably represents C-C8-alkyl, C 2 -C8-alkoxy, C2-C8-alkylamno, dC8-alkyOamno, C2-C8-alkyltho, C3-C4-alkenyltho, C3-C5-cycloalkyltho or represents phenyl, phenoxy or phenyltho, each of whch s optonally monosbsttted by florne, chlorne, bromne, ntro, cyano, C-C3-alkoxy, C-C3-haloalkoxy, C2-alkyltho, C2- C3-haloalkyltho, C2-alkyl of trfloromethyl, R partclarly preferably represents C-C6-alkoxy or C-Ce-alkyltho, R partclarly preferably represents hydro8en, C-C8-alkyl, C3-C6-cycloalkyl, C2-C8alkoxy, C3-C5-alkenyl, C2-C8-alkoxy-C-alkyl, represents phenyl whch s optonally monosbsttted by florne, chlorne, bromne, trfloromethyl, C2-C-alkyl or C-C4- alkoxy, represents benzyl whch s optonally monosbsttted by florne, chlorne, bromne, -C4-alkyl, trfloromethyl or C \ -C4~alkoxy, R7 partclarly preferably represents C-C6-alkyl, C3-C6-alkenyl or C-C6-alkoxy-C-C4-alkyl, R and R7 to8ether partclarly preferably represent an optonally methyl- or ethyl-sbsttted C4- C5-alkylene radcal n whch optonally one methylene 8rop s replaced by oxy8en or slfr. n the radcal defntons mentoned as ben8 partclarly preferred, halo8en represents florne, chlorne and bromne, n partclar florne and chlorne. 2 very partclarly preferably represents odne, X very partclarly preferably represents hydro8en, florne, chlorne, bromne, methyl, ethyl, propyl, methoxy or ethoxy, Y very partclarly preferably represents hydro8en, chlorne, bromne, methyl, ethyl, propyl, methoxy or ethoxy, wth the provso that at least one of the radcals 2, X or Y s located n the 2-poston of the phenyl radcal and s not hydro8en. Here, the radcals 2, X and Y, havn8 ther very partclarly preferred meann8s, are very partclarly preferably present n the follown8 phenyl sbsttton patterns (Figre Removed) where only n the phenyl sbsttton pattern (8) X may also represent hydro8en. CKE very partclarly preferably represents one of the 8rops (Figre Removed) A very partclarly preferably represents hydro8en, represents C2-Calkyl or C2-C2-alkoxy- -C2-alkyl, each of whch s optonally mono- to trsbsttted by florne, represents cyclopropyl, cyclopentyl or cyclohexyl and, only n the case of the componds of the formla (-5), represents phenyl whch s optonally mono- to dsbsttted by florne, chlorne, bromne, methyl, ethyl, n-propyl, sopropyl, methoxy, ethoxy, trfloromethyl, trfloromethoxy, cyano or ntro, B very partclarly preferably represents hydro8en, methyl or ethyl, or A, B and the carbon atom to whch they are attached very partclarly preferably represent satrated C5-C8-cycloalkyl n whch optonally one rn8 member s replaced by oxy8en or slfr and whch s optonally monosbsttted by methyl, ethyl, propyl, sopropyl, trfloromethyl, methoxy, ethoxy, propoxy, methoxyethoxy, btoxy or ethoxyethoxy, wth the provso that n ths case very partclarly preferably represents hydro8en, or A, B and the carbon atom to whch they are attached very partclarly preferably represent C8cycloalkyl whch s optonally sbsttted by alkylenedoxyl 8rop whch contans wth two not drectly ad2acent oxy8en atoms, wth the provso that n ths case very partclarly preferably represents hydro8en, or A, B and the carbon atom to whch they are attached very partclarly preferably represent 05- C8-cycloalkyl or C5-C8-cycloalkenyl n whch two sbsttents to8ether wth the carbon atoms to whch they are attached represent C2-C4-alkanedyl or C2-C4-alkenedyl or btadenyl, wth the provso that n ths case -' very partclarly preferably represents hydro8en, D very partclarly preferably represents hydro8en, represents -C4-alkyl, C3-C4-alkenyl, C2-C4-alkoxy-C2-C3-alkyl, each of whch s optonally mono- to trsbsttted by florne, represents cyclopropyl, cyclopentyl or cyclohexyl or (bt not n the case of the componds of the formlae (-)) represents phenyl or pyrdyl, each of whch s optonally monosbsttted by florne, chlorne, methyl, ethyl, n-propyl, sopropyl, methoxy, ethoxy or trfloromethyl, or A and D to8ether very partclarly preferably represent C3-C5-alkanedyl whch s optonally monosbsttted by methyl or methoxy and n whch optonally one carbon atom s replaced by oxy8en or slfr or represent the 8rop AD-, A and ! to8ether very partclarly preferably represent C3-C4-alkanedyl whch s optonally mono- or dsbsttted by methyl or methoxy, or ! very partclarly preferably represents hydro8en, 2 very partclarly preferably represents hydro8en, 4, and * ndependently of one another very partclarly preferably represent hydro8en or methyl, very partclarly preferably represents hydro8en, methyl, ethyl or propyl, or 3 and to8ether wth the carbon to whch they are attached very partclarly preferably represent a satrated C5-C5-rn8 whch s optonally monosbsttted by methyl or methoxy, wth the provso that n ths case A very partclarly preferably represents hydro8en, 8 very partclarly preferably represents hydro8en (a) or represents one of the 8rops R. very partclarly preferably represents C-C8-alkyl, C2-C27-alkenyl, C2-C2-alkoxy-Calkyl, C-C2-akyltho-C-alkyl, each of whch s optonally monosbsttted by chlorne, or represents cyclopropyl or cyclohexyl, each of whch s optonally monosbsttted by florne, chlorne, methyl or methoxy, very partclarly preferably represents phenyl whch s optonally monosbsttted by florne, chlorne, bromne, cyano, ntro, methyl, methoxy, trfloromethyl or trfloromethoxy, R2 very partclarly preferably represents C-C8-alkyl, C2-C8-alkenyl or C-C4-alkoxy-C2- C3-alkyl, each of whch s optonally monosbsttted by florne, or represents phenyl or benzyl, R3 very partclarly preferably represents CpC8-alkyl. 2 especally preferably represents odne, X especally preferably represents hydro8en, chlorne, methyl or ethyl, Y especally preferably represents hydro8en, chlorne, methyl or ethyl, wth the provso that at least one of the radcals 2, X or Y s located n the 2-poston of the phenyl radcal and s not hydro8en. Here, the radcals 2, X and Y, havn8 ther especally preferred meann8s, are especally preferably present n the follown8 phenyl sbsttton patterns where only n the phenyl sbsttton pattern (8) X may also represent hydro8en, CKE especally preferably represents one of the 8rops A especally preferably represents C-Calky! or cyclopropyl, B especally preferably represents hydro8en or methyl, A, B and the carbon atom to whch they are attached especally preferably represent satrated C5- C6-cycloalkyl n whch optonally one rn8 member s replaced by oxy8en and whch s optonally monosbsttted by methyl, methoxy or propoxy, D especally preferably represents hydro8en, or A and D to8ether especally preferably represent the 8rop AD-, n the case of CKE = 8rop (8) A and D to8ether especally preferably represent C3-C5-alkanedyl, 8 especally preferably represents hydro8en (a) or represents one of the 8rops R. especally preferably represents -C6-alkyl, C-C2-alkoxy-C-alkyl, cyclopropyl, each of whch s optonally monosbsttted by chlorne, or represents phenyl whch s optonally monosbsttted by chlorne, R.2 especally preferably represents C2-C8-alkyl C2-C8-alkenyl or benzyl. The 8eneral or preferred radcal defntons or llstratons 8ven above can be combned wth one another as desred, .e. ncldn8 combnatons between respectve ran8es and preferred ran8es. They apply both to the end prodcts and, correspondn8ly, to precrsors and ntermedates. Preference accordn8 to the nventon s 8ven to the componds of the formla () whch contan a combnaton of the meann8s 8ven above as ben8 preferred (preferable). Partclar preference accordn8 to the nventon s 8ven to the componds of the formla () whch contan a combnaton of the meann8s 8ven above as ben8 partclarly preferred. Very partclar preference accordn8 to the nventon s 8ven to the componds of the formla () whch contan a combnaton of the meann8s 8ven above as ben8 very partclarly preferred. Specal preference accordn8 to the nventon s 8ven to the componds of the formla () whch contan a combnaton of the meann8s 8ven above as ben8 especally preferred. Satrated or nsatrated hydrocarbon radcals, sch as alkyl, alkanedyl or alkenyl, can n each case be stra8ht-chan or branched as far as ths s possble, ncldn8 n combnaton wth heteroatoms, sch as, for example, n alkoxy. nless ndcated otherwse, optonally sbsttted radcals can be mono- or polysbsttted, where n the case of polysbsttton the sbsttents can be dentcal or dfferent. n addton to the componds mentoned n the preparaton examples, partclar menton may be made of the follown8 componds of the formla (-l-a): (Figre Removed) Preferred defntons of the 8rops lsted above n connecton wth the crop plant compatbltymprovn8 componds ("herbcde safeners") of the formlae (la), (lb), (He), (ld) and (He) are 5 defned below. m preferably represents the nmbers 0, , 2, 3 or 4. A preferably represents one of the dvalent heterocyclc 8ropn8s shown below n preferably represents the nmbers 0, , 2, 3 or 4. 20 A2 preferably represents n each case optonally methyl-, ethyl-, methoxycarbonyl- or ethoxycarbonyl-sbsttted methylene or ethylene. R4 preferably represents hydroxyl, mercapto, amno, methoxy, ethoxy, n- or -propoxy, n-, -, sor t-btoxy, methyltho, ethyltho, n- or -propyltho, n-, -, s- or t-btyltho, methylamno, ethylamno, n- or -propylamno, n-, -, s- or t-btylamno, dmethylamno or dethylamno. R5 preferably represents hydroxyl, mercapto, amno, methoxy, ethoxy, n- or -propoxy, n-, -, sor t-btoxy, -methylhexyloxy, allyloxy, -allyloxymethylethoxy, methyltho, ethyltho, n- or -propyltho, n-, -, s- or t-btyltho, methylamno, ethylamno, n- or -propylamno, n-, -, sor t-btylamno, dmethylamno or dethylamno. R6 preferably represents n each case optonally florne-, chlorne- and/or bromne-sbsttted methyl, ethyl, n- or -propyl. R7 preferably represents hydro8en, n each case optonally florne- and/or chlorne-sbsttted methyl, ethyl, n- or -propyl, n-, -, s- or t-btyl, propenyl, btenyl, propynyl or btynyl, methoxymethyl, ethoxymethyl, methoxyethyl, ethoxyethyl, doxolanylmethyl, fryl, frylmethyl, thenyl, thazolyl, pperdnyl, or optonally florne-, chlorne-, methyl-, ethyl-, n- or -propyl-, n-, -, s- or t-btyl-sbsttted phenyl. R8 preferably represents hydro8en, n each case optonally florne- and/or chlorne-sbsttted methyl, ethyl, n- or -propyl, n-, -, s- or t-btyl, propenyl, btenyl, propynyl or btynyl, methoxymethyl, ethoxymethyl, methoxyethyl, ethoxyethyl, doxolanylmethyl, fryl, frylmethyl, thenyl, thazolyl, pperdnyl, or optonally florne-, chlorne-, methyl-, ethyl-, n- or -propyl-, n-, -, s- or t-btyl-sbsttted phenyl, or to8ether wth R7 represents one of the radcals -CH2-O-CH2-CH2- and -CH2-CH2-O-CH2-CH2- whch are optonally sbsttted by methyl, ethyl, fryl, phenyl, a fsed benzene rn8 or by two sbsttents whch, to8ether wth the C atom to whch they are attached, form a 5- or 6-membered carbocycle. R9 preferably represents hydro8en, cyano, florne, chlorne, bromne, or represents n each case optonally florne-, chlorne- and/or bromne-sbsttted methyl, ethyl, n- or -propyl, cyclopropyl, cyclobtyl, cyclopentyl, cyclohexyl or phenyl. R20 preferably represents hydro8en, optonally hydroxyl-, cyano-, florne-, chlorne-, methoxy-, ethoxy-, n- or -propoxy-sbsttted methyl, ethyl, n- or -propyl, n-, -, s- or t-btyl. R2 preferably represents hydro8en, cyano, florne, chlorne, bromne, or represents n each case optonally florne-, chlorne- and/or bromne-sbsttted methyl, ethyl, n- or -propyl, n-, -, s- or t-btyl, cyclopropyl, cyclobtyl, cyclopentyl, cyclohexyl or phenyl. X preferably represents ntro, cyano, florne, chlorne, bromne, methyl, ethyl, n- or -propyl, n-, -, s- or t-btyl, dfloromethyl, dchloromethyl, trfloromethyl, trchloromethyl, chlorodfloromethyl, florodchloromethyl, methoxy, ethoxy, n- or -propoxy, dfloromethoxy or trfloromethoxy. X2 preferably represents hydro8en, ntro, cyano, florne, chlorne, bromne, methyl, ethyl, n- or -propyl, n-, -, s- or t-btyl, dfloromethyl, dchloromethyl, trfloromethyl, trchloromethyl, chlorodfloromethyl, florodchloromethyl, methoxy, ethoxy, n- or -propoxy, dfloromethoxy or trfloromethoxy. X3 preferably represents hydro8en, ntro, cyano, florne, chlorne, bromne, methyl, ethyl, n- or -propyl, n-, -, s- or t-btyl, dfloromethyl, dchloromethyl, trfloromethyl, trchloromethyl, chlorodfloromethyl, florodchloromethyl, methoxy, ethoxy, n- or -propoxy, dfloromethoxy or trfloromethoxy. t preferably represents the nmbers 0, , 2, 3 or 4: v preferably represents the nmbers 0, , 2, or 3. R22 preferably represents hydro8en, methyl, ethyl, n- or -propyl. R23 preferably represents hydro8en, methyl, ethyl, n- or -propyl. R24 preferably represents hydro8en, n each case optonally cyano-, florne-, chlorne-, methoxy-, ethoxy-, n- or -propoxy-sbsttted methyl, ethyl, n- or -propyl, n-, -, s- or t-btyl, methoxy, ethoxy, n- or -propoxy, n-, -, s- or t-btoxy, methyltho, ethyltho, n- or -propyltho, n-, -, s- or t-btyltho, methylamno, ethylamno, n- or -propylamno, n-, -, sor t-btylamno, dmethylamno or dethylamno, or n each case optonally cyano-, florne-, chlorne-, bromne-, methyl-, ethyl-, n- or -propyl-sbsttted cyclopropyl, cyclobtyl, cyclopentyl, cyclohexyl, cyclopropyloxy, cyclobryloxy, cyclopentyloxy, cyclohexyloxy, cyclopropyltho, cyclobtyltho, cyclopentyltho, cyclohexyltho, cyclopropylamno, cyclobtylamno, cyclopentylamno or cyclohexylamno. R25 preferably represents hydro8en, n each case optonally cyano-, hydroxyl-, florne-, chlorne-, methoxy-, ethoxy-, n- or -propoxy-sbsttted methyl, ethyl, n- or -propyl, n-, - or s-btyl, n each case optonally cyano-, florne-, chlorne- or bromne-sbsttted propenyl, btenyl, propynyl or btynyl, or n each case optonally cyano-, florne-, chlorne-, bromne-, methyl-, ethyl-, n- or -propyl-sbsttted cyclopropyl, cyclobtyl, cyclopentyl or cyclohexyl. R2 preferably represents hydro8en, n each case optonally cyano-, hydroxyl-, florne-, chlorne-, methoxy-, ethoxy-, n- or -propoxy-sbsttted methyl, ethyl, n- or -propyl, n-, - or s-btyl, n each case optonally cyano-, florne-, chlorne- or bromne-sbsttted propenyl, btenyl, propynyl or btynyl, n each case optonally cyano-, florne-, chlorne-, bromne-, methyl-, ethyl-, n- or -propyl-sbsttted cyclopropyl, cyclobtyl, cyclopentyl or cyclohexyl, or optonally ntro-, cyano-, florne-, chlorne-, bromne-, methyl-, ethyl-, n- or -propyl-, n-, -, s- or t-btyl-, trfloromethyl-, methoxy-, ethoxy-, n- or -propoxy-, dfloromethoxy- or trfloromethoxy-sbsttted phenyl, or to8ether wth R25 represents n each case optonally methyl- or ethyl-sbsttted btane- ,4-dy (trmethylene), pentane-l,5-dyl, -oxabtane- ,4-dyl or 3-oxapentane-l,5-dyl. X4 preferably represents ntro, cyano, carboxyl, carbamoyl, formyl, slfamoyl, hydroxyl, amno, florne, chlorne, bromne, methyl, ethyl, n- or -propyl, n-, -, s- or t-btyl, trfloromethyl, methoxy, ethoxy, n- or -propoxy, dfloromethoxy or trfloromethoxy. X5 preferably represents ntro, cyano, carboxyl, carbamoyl, formyl, slphamoyl, hydroxyl, amno, florne, chlorne, bromne, methyl, ethyl, n- or -propyl, n-, -, s- or t-btyl, trfloromethyl, methoxy, ethoxy, n- or -propoxy, dfloromethoxy or trfloromethoxy. Examples of the componds of the formla (la) whch are very partclarly preferred as herbcde safeners accordn8 to the nventon are lsted n the table below. Table Examples of the componds of the formla (Ha) (Figre Removed) Most preferred as crop plant compatblty-mprovn8 compond [component (b')] are clontocetmexyl, fenchlorazole-ethyl, soxadfen-ethyl, mefenpyr-dethyl, frlazole, fenclorm, cmylron, dymron, dmepperate and the componds e-5 and e-, and partclar emphass s 8ven to clontocet-mexyl and mefenpyr-dethyl. The componds of the 8eneral formla (Ha) to be sed as safeners accordn8 to the nventon are known and/or can be prepared by processes known per se (cf. WO-A-9/07874, WO-A-95/07897). The componds of the 8eneral formla (lb) to be sed as safeners accordn8 to the nventon are known and/or can be prepared by processes known per se (cf. EP-A-9736). The componds of the 8eneral formla (He) to be sed as safeners accordn8 to the nventon are known and/or can be prepared by processes known per se (cf. DE-A-228097, DE-A-2350547). The componds of the 8eneral formla (ld) to be sed as safeners accordn8 to the nventon are known and/or can be prepared by processes known per se (cf. DE-A-962522/S-A-6235680). The componds of the 8eneral formla (He) to be sed as safeners accordn8 to the nventon are known and can be prepared by processes known per se (cf. WO-A-99/66795/S-A-625827). Examples of the selectve herbcdal combnatons accordn8 to the nventon comprsn8 n each case one actve compond of the formla () and one of the safeners defned above are lsted n the table below. t has now srprsn8ly been fond that the above-defned actve-compond combnatons of odophenyl-sbsttted cyclc ketoenols of the 8eneral formla () and safeners (antdotes) from the 8rop (b') set ot above combne very 8ood sefl plant tolerance wth a h8h herbcdal actvty and can be sed n varos crops, n partclar n cereals (especally wheat), bt also n soya beans, potatoes, corn and rce, for selectve weed control. n ths context t s consdered srprsn8 that, from a mltplcty of known safeners or antdotes capable of anta8onzn8 the dama8n8 effect of a herbcde on the crop plants, t s specfcally the componds of 8rop (b') set ot above whch are stable for compensatn8 - almost completely - the dama8n8 effect of sbsttted cyclc ketoenols on the crop plants, wthot at the same tme havn8 any crtcal adverse effect on the herbcdal actvty a8anst the weeds. Emphass may be 8ven here to the partclarly advanta8eos effect of the partclarly preferred and most preferred combnaton partners from 8rop (b'), partclarly wth re8ard to the 8entle treatment of cereal plants, sch as wheat, barley and rye, for example, bt also corn and rce, as crop plants. sn8, for example, accordn8 to process (A) ethyl N-(2,6-dmethyl-4-odophenylacetyl)-l-amnocyclohexanecarboxylate as startn8 materal, the corse of the process accordn8 to the nventon can be represented by the reacton scheme below: sn8, for example, accordn8 to process (B) ethyl O-(2,6-dmethyl-4-odophenylacetyl)-2- hydroxysobtyrate, the corse of the process accordn8 to the nventon can be represented by the reacton scheme below: (Figre Removed) n8, for example, accordn8 to process (C) ethyl 2-(2,6-dmethyl-4-odophenyl)-4-(4- methoxy)benzylmercapto-4-methyl-3-oxovalerate, the corse of the process accordn8 to the nventon can be represented by the reacton scheme below: n8, for example, accordn8 to process (D) chlorocarbonyl 2-[(2,6-dmethyl-4-odophenyl)] ketene and acetone as startn8 materals, the corse of the process accordn8 to the nventon be represented by the reacton scheme below: sn8, for example, accordn8 to process (E) chlorocarbonyl 2-(2,6-dmethyl-4-odophenyl) ketene and thobenzamde as startn8 materals, the corse of the process accordn8 to the nventon can be represented by the reacton scheme below: sn8, for example, accordn8 to process (F) ethyl 5-(2,6-dmethyl-4-odophenyl)-2,3- trmethylene-4-oxovalerate, the corse of the process accordn8 to the nventon can be oxohexanoate, the corse of the process accordn8 to the nventon can be represented by the reacton scheme below: sn8, for example, accordn8 to process (Ha) hexahydropyrdazne and chlorocarbonyl 2 dmethyl-4-odo)phenyl] ketene as startn8 materals, the corse of the reacton of the process accordn8 to the nventon can be represented by the reacton scheme below: n8, for example, accordn8 to process (Hp) hexahydropyrdazne and dmethyl 2-(2,6-dmethyl- 4-odo)phenylmalonate as startn8 materals, the corse of the process accordn8 to the nventon can be represented by the reacton scheme below: sn8, for example, accordn8 to process (B) 3-(2,6-dmethyl-4-odophenyl)-5,5- dmethylpyrroldne-2,4-done and acetc anhydrde as startn8 materals, the corse of the process accordn8 to the nventon can be represented by the reacton scheme below: sn8, for example, accordn8 to process (2) 8-[(2,6-dmethyl-4-odo)phenyl]-l-azabcyclo- (4.3.()l'6)-nonane-7,9-done and ethyl chloroformate as startn8 materals, the corse of the process accordn8 to the nventon can be represented by the reacton scheme below: sn8, for example, accordn8 to process (K) 3-(2,6-dmethyl-4-odophenyl)-4-hydroxy-5-methyl- 6-(3-pyrdyl)pyrone and methyl chloromonothoformate as startn8 materals, the corse of the reacton can be represented as follows: sn8, for example, accordn8 to process (L) 3-(2,6-dmethyl-4-odophenyl)-5,5-pentamethylenepyrroldne- 2,4-done and methaneslfonyl chlorde as startn8 materal, the corse of the reacton can be represented by the reacton scheme below: sn8, for example, accordn8 to process (M) 3-(2,6-dmethyl-4-odophenyl)-4-hydroxy-5,5-dmethylpyrroldne- 2,4-done and 2,2,2-trfloroethyl methanethophosphonyl chlorde as startn8 materals, the corse of the reacton can be represented by the reacton scheme below: (Figure Removed) sn8, for example, accordn8 to process (N) 3-(2-ethyl-4-odo-6-methylphenyl]-5-cyclopropyl-5- methylpyrroldne-2,4-done and NaOH as components, the corse of the process accordn8 to the nventon can be represented by the reacton scheme below: sn8, for example, accordn8 to process (O) varant a 3-(2,6-dmethyl-4-odophenyl)-4-hydroxy- 5,5-tetramethylene-A--dhydrofran-2-one and ethyl socyanate as startn8 materals, the corse of the reacton can be represented by the reacton scheme below: sn8, for example, accordn8 to process (O) varant 6 3-(2-methyl-4-odo-6-ethylphenyl)-5- methylpyrroldne-2,4-done and dmethylcarbamoyl chlorde as startn8 materals, the corse of the reacton can be represented by the scheme below: (Figure Removed) sn8, for example, accordn8 to process (P) 3-(4-bromo-2,6-dmethylphenyl)-5,5-dmethylpyrroldne- 2,4-done and sodm methoxde as startn8 materals, the corse of the reacton can be represented by the scheme below: The componds, rered as startn8 materals for the process (a) accordn8 to the nventon, of checker: Above, please chan8e T to T n whch A, B, D, 2, X, Y and R8 are as defned above are novel. The acylamno acd esters of the formla () are obtaned, for example, when amno acd dervatves of the formla (XX) A, B, R8 and D are as defned above are acylated wth sbsttted phenylacetc acd dervatves formla (XXFV) 2, X and Y are as defned above and Z represents a leavn8 8rop ntrodced by rea8ents, sch as carbonyldmdazole, carbonyldmdes (sch as, for example, dcyclohexylcarbondmde), phosphorylatn8 a8ents (sch as, for example, POC3, BOP-C), halo8enatn8 a8ents, for example thonyl chlorde, oxalyl chlorde, phos8ene or chloroformc esters, for actvatn8 carboxylc acds (Chem. Revews 52, 237-46 (953); Bhattacharya, ndan 2. Chem. 6, 34-5, 968) or when acylamno acds of the formla (XXV) A, B, D, 2, X and Y are as defned above are esterfed (Chem. nd. (London) 568 (968)). The componds of the formla (XXV) . A, B, D, 2, X and Y are as defned above are novel. The componds of the formla (XXV) are obtaned when amno acds of the formla (XXV) (Figure Removed) A, B and D are as defned above are acylated wth sbsttted phenylacetc acd dervatves of the formla (XXV) 2, X and Y are as defned above and Z s as defned above, for example accordn8 to Schotten-Bamann (Or8ankm, VEB Detscher Verla8 der Wssenschaften, Berln 977, p. 505). The componds of the formla (XXV) are novel. They can be prepared by processes known n prncple and as llstrated n the examples (see, for example, H. Henecka, Hoben-Weyl, Methoden der Or8anschen Cheme [Methods of Or8anc Chemstry], Vol. 8, pp. 467-469 (952)). The componds of the formla (XXV) are obtaned, for example, by reactn8 sbsttted wth halo8enatn8 a8ents (for example thonyl chlorde, thonyl bromde, oxalyl chlorde, phos8ene, phosphors trchlorde, phosphors trbromde or phosphors pentachlorde), phosphonylatn8 a8ents, sch as (for example POC, BOP-C), carbonyldmdazole, carbonyldmdes (for example dcyclohexylcarbonyldmde), f approprate n the presence of a dlent (for example optonally chlornated alphatc or aromatc hydrocarbons, sch as tolene or methylene chlorde, or ethers, for example tetrahydrofran, doxane, methyl tert-btyl ether) at temperatres of from -20°C to 50°C, preferably from -0°C to 00°C. Some of the componds of the formlae (XX) and (XXV) are known, and/or they can be prepared by known processes (see, for example, Compa8non, Moce Ann. Chm. (Pars) [4] The sbsttted cyclc amnocarboxylc acds of the formla (XXV) n whch A and B form a rn8 are 8enerally obtanable by the Bcherer-Ber8s synthess or by the Strecker synthess, where they are obtaned n dfferent somerc forms. Ths, the condtons of the Bcherer-Ber8s synthess afford predomnantly the somers (herenbelow for the sake of smplcty referred to as p) n whch the radcals R and the carboxyl 8rop are n eatoral postons, whereas the condtons of the Strecker synthess afford predomnantly the somers (herenbelow for the sake of smpcty referred to as a) n whch the amno 8rop and the radcals R are n eatoral postons. Bcherer-Ber8s synthess Strecker synthess (B somer) (a somer) (L. Mnday, 2. Chem. Soc. 4372 (96); 2.T. Eward, C. 2tran8er, Can. 2. Chem. 53, 3339 sed n the above process (A), of the formla () A, B, D, 2, X, Y and R8 are as defned above can frthermore be prepared by reactn8 amnontrles of the formla (XXV) (Figure Removed) A, B and D are as defned above wth sbsttted phenylacetc acd dervatves of the formla (XXV) (Figure Removed) A, B, D, 2, X and Y are as defned above and then sb2ectn8 these to an acdc alcoholyss. The componds of the formla (XXX) are lkewse novel. The componds, rered as startn8 materals n the process (B) accordn8 to the nventon, of They can be prepared by methods known n prncple. Ths, the componds of the formla () are obtaned, for example, when 2-hydroxycarboxylc esters of the formla (XXX-A) A, B and R are as defned above are acylated wth sbsttted phenylacetc acd dervatves of the formla (XXV) 2, X, Y and Z are as defned above (Chem. Revews 52, 237-46 (953)). Frthermore, componds of the formla () are obtaned when sbsttted phenylacetc acds of the formla (XXV) 2, X and Y are as defned above are alkylated wth a-halocarboxylc esters of the formla (XXX-B) A, B and R8 are as defned above and Hal represents chlorne or bromne. Some of the componds of the formla (XXV) are commercally avalable, some are known; however, some are also novel. The componds of the formla (XXX-B) are commercally avalable. The componds of the formla (XXV) 2, X and Y are as defned above are obtaned, for example, when phenylacetc esters of the formla (XXX) (Figure Removed) 2, X, Y and R8 are as defned above are hydrolyzed n the presence of acds or bases, n the presence of a solvent nder 8enerally known standard condtons. Some of the componds of the formla (XXX) are commercally avalable, some are known, for example from WO 0/7973; however, some are also novel. The componds of the formla (XXX) 2, X, Y and R are as defned above are frthermore obtaned by the process () descrbed n the examples when phenylacetc esters of the formla (XXX-a) R8, X and Y are as defned above are reacted n the presence of oddes (preferably sodm odde or potassm odde) n the presence of a base and, f approprate, n the presence of a catalyst (preferably copper salts, sch as, for example, copper() odde). The phenylacetc esters of the formla (XXX-a) are known n prncple, for example from the applcatons WO 96/35 664, WO 97/02243, WO 97/0535, WO 98/05638 and DE-A-0 30 and they can be prepared by the processes descrbed n these pblcatons. The componds, rered as startn8 materals for the process (C) above, of the formla (FV) A, B, 2, V, X, Y and R8 are as defned above are novel. They can be prepared by methods known n prncple. The componds of the formla (FV) are obtaned, for example, when sbsttted phenylacetc esters of the formla (XXX) 2, X, Y and R8 are as defned above are acylated wth 2-benzylthocarbonyl haldes of the formla (XXX) A, B and V are as defned above and Hal represents halo8en (n partclar chlorne or bromne) n the presence of stron8 bases (see, for example, M.S. Chambers, E.2. Thomas, D.2. Wllams, 2. Chem. Soc. Chem. Commn., (987), 228). Some of the benzylthocarbonyl haldes of the formla (XXX) are known, and/or they can prepared by known processes (2. Antbotcs (983), 26, 589). The halocarbonyl ketenes of the formla (V) rered as startn8 materals for the above (D), (E) and (H-ot) are novel. They can be prepared by methods known n prncple (cf., for example, Or8. Prep. Proced. nt., 7, (4), 55-58, 975 and DE 945 703). Ths, for example, are reacted wth acd haldes, sch as, for example, thonyl chlorde, phosphors(V) chlorde, phosphors() chlorde, oxalyl chlorde, phos8ene or thonyl bromde, f approprate n the presence of catalysts, sch as, for example, dmethylformamde, methylsterylformamde or trphenylphosphne, and, f approprate, n the presence of bases, sch as, for example, pyrdne or trethylamne. Some of the sbsttted phenylmalonc acds of the formla (XXX) are known or commercally avalable; however, some are also novel. They can be prepared n a smple manner by known processes (cf., for example, Or8ankm, VEB Detscher Verla8 der Wssenschaften, Berln 977, p. 57 ff, EP-A-528 56, WO 96/35 664, WO 97/02 243, WO 97/0535, WO 97/36868 and WO 98/05638). Ths, phenylmalonc acds of the formla (XXX) 2, X and Y are as defned above are obtaned when phenylmalonc esters of the formla (X) (Figure Removed) are ntally hydrolyzed n the presence of a base and of a solvent and then careflly acdfed for example, EP-A-528 56, WO 96/35 664, WO 97/02 243). The malonc esters of the formla (X) 2, X and Y are as defned above and represents OR8 or NH2, where R8 s as defned above, are known (for example WO 0/07973, Larock et al., Tetrahedron 52 2743 ff. (996); however, some are also novel. They can be prepared by 8enerally known methods of or8anc chemstry (cf., for example, Tetrahedron Lett. 27, 2763 (986), Or8ankm VEB Detscher Verla8 der Wssenschaften, Berln 977, p. 587 ff., WO 96/35664, WO 97/02243, WO 97/0535, WO 97/36868, WO 98/05638 and WO 99/47525). The carbonyl componds, rered as startn8 materals for the process (D) accordn8 to the nventon, of the formla (V) or slylenol ethers thereof of the formla (Va) A, D and R8 are as defned above are commercally avalable componds, 8enerally known componds or componds whch can be obtaned by known processes. The preparaton of the ketene acd chlordes of the formla (V) rered as startn8 materals for carryn8 ot the process (E) accordn8 to the nventon have already been descrbed above. The thoamdes, rered for carryn8 ot the process (E) accordn8 to the nventon, of the formla (Figure Removed) in whichis as defined aboveare compounds which are enerally known in oranic chemistry. The compounds, required as startin materials in the above process (F), of the formula (VIII) (Figure Removed) in whichThey can be prepared by methods known in principle. The 5-aryl-4-ketocarboxylic esters of the formula (VIII) are obtained, for example, when 5-aryl-ketocarboxylic acids of the formula (XXXIV)in which, X, Y, A, B, Q and Q2 are as defined aboveare esterified (cf, for example, Oranikum, 5th edition, Berlin, 977, pae 499) or alkylated (seePreparation Example). The 5-aryl-4-ketocarboxylic acids of the formula (XXXIV) (Figure Removed) in whichA, B, , Q, Q2, X and Y are as defined above are novel; however, they can be prepared by methods known in principle (WO 96/0 79, WO 97/4667, WO 9/392).The 5-aryl-4-ketocarboxylic acids of the formula (XXXFV) are obtained, for example, when 2-phenyl-3-oxoadipic esters of the formula (XXXV) in whichA, B, , Ql, Q2, X and Y are as defined above and R. and R° represent alkyl (in particular C]-C-alkyl) and, when the compound of the formula (XXXVII-a) is used, R represents hydroen, are decarboxylated, if appropriate in the presence of a diluent and if appropriate in the presence of a base or acid (cf., for example, Oranikum, 5th edition, Berlin, 977, pae 59 to 52, WO 96/079, WO 97/4667, WO 9/392). The compounds of the formula (XXXV) A, B, , Q, Q2, X, Y, R, R' are as defined above and, when the compound of the formula (XXXVII-a) is used, R represents hydroen are novel.The compounds of the formula (XXXV) are obtained, for example, when dicarboxylic monoester chlorides of the formula (XXXVI), A, B, Q!, Q2 and R are as defined above and Hal represents chlorine or bromine or carboxylic anhydrides of the formula (XXXVII-a) A, B, Q! and Q2 are as defined above are acylated with a phenylacetic ester of the formula (XXXI) , X, Y and R' are as defined above in the presence of a diluent and in the presence of a base (cf., for example, M.S. Chambers, E. .Thomas, D.. Williams, . Chem. Soc. Chem. Commun., (97), 22, cf. also the PreparationExamples). Some of the compounds of the formulae (XXXVI) and (XXXVII-a) are known compounds oforanic chemistry, and/or they can be prepared in a simple manner by methods known in principle.The compounds, required as startin materials in the above process (), of the formula (IX)A, B, , Q3, Q4, Q5, Q6, X, Y and R are as defined above are novel.They can be prepared by methods known in principle. The 6-aryl-5-ketocarboxylic esters of the formula (IX) are obtained, for example, when 6-aryl-5-ketocarboxylic acids of the formula (XXXVIII) are esterified (cf., for example, Oranikum, 5th edition, Berlin, 977, pae 499, WO The 6-aryl-5-ketocarboxylic acids of the formula (XXXVIII) A, B, , Q3, Q4, Q5, Q6, X and Y are as defined above are novel. They can be prepared by methods known in principle (WO 99/43649, WO substituted 2-phenyl-3-oxoheptanedioic esters of the formula (XXXIX) A, B, , Q3, Q4, Q5, Q6, X and Y are as defined above and R. and R' represent alkyl (preferably C-C-alkyl) and, when the compound of the formula (XXXVII-b) is used, R represents hydroen, are hydrolyzed and decarboxylated, if appropriate in the presence of a diluent and if appropriate inthe presence of a base or acid (cf., for example, Oranikum, 5th edition, Berlin, 977, paes to 52, WO 99/43649, WO 99/469).The compounds of the formula (XXXIX)A, B, , Q3, Q4, Q5, Q6, x, Y, R and R' are as defined aboveare novel and can be obtainedwhen dicarboxylic esters of the formula (XL)A, B, Q3, Q4, Q5, Q6 and R are as defined above or carboxylic anhydrides of the formula (XXXVII-b)(XXXVII-b)in which A, B, Q3, Q4, Q5, Q6 are as defined aboveare condensed with a substituted phenylacetic ester of the formula (XXXI) (Figure Removed) , X, Yand R' are as defined abovein the presence of a diluent and in the presence of a base. Some of the compounds of the formula (XL) are known, and/or they can be prepared by knownprocesses.Some of the hydrazines, required as startin materials for the process (H-a) and (H-B) accordin tothe invention, of the formula (X)A and D are as defined above are known, and/or they can be prepared by methods known from the literature (cf., for example,Liebis Ann. Chem. 55, 6 (954); Reaktionen der oranischen Synthese [Reactions of OranicSynthesis], C. Ferri, paes 22, 53; eor Thieme Verla Stuttart, 97; Liebis Ann. Chem. 443. 242 (925); Chem. Ber. 9, 255 (965), EP-A-50 26, WO 92/650, WO 99/47 525, The compounds, required for the process (H-y) accordin to the invention, of the formula in whichA, D, , X, Y and R are as defined above are novel.The acylcarbazates of the formula (XII) are obtained, for example, when carbazates of the (Figure Removed) A, R. and D are as defined aboveare acylated with substituted phenylacetic acid derivatives of the formula (XXFV), X, Y and Z are as defined above(Chem. Reviews 52, 237-46 (953); Bhattacharya, Indian . Chem. 6, 34-5, 96).Some of the carbazates of the formula (XLI) are commercially available compounds and, or they can be prepared by processes of oranic chemistry known in principle.The compounds of the formula (XXFV) have already been described in connection with theintermediates for the process (A) and (B).The acid halides of the formula (XIII), carboxylic anhydrides of the formula (XIV), chloroformic esters or chloroformic thioesters of the formula (XV), chloromonothioformic esters or chlorodithioformic esters of the formula (XVI), sulfonyl chlorides of the formula (XVII), phosphorus compounds of the formula (XVIII) and metal hydroxides, metal alkoxides or amines ofthe formulae (XIX) and (XX) and isocyanates of the formula (XXI) and carbamoyl chlorides of theformula (XXII) furthermore required as startin materials for carryin out the processes (I), (K), (L), (M), (N) and (O) accordin to the invention are enerally known compounds of oranicor inoranic chemistry. In addition, the compounds of the formulae (V), (VII), (XIII) to (XXII), (XXIII), (XXVI), (XXVIII), (XXX-A), (XXX-B), (XXXII), (XXXVI), (XXXVII-a), (XXXVII-b), (XL) and are furthermore known from the patent applications cited at the outset, and/or they can be preparedby the methods stated in these publications. The process (A) is characterized in that compounds of the formula (II) in which A, B, D, , and R° are as defined above are subected to an intramolecular condensation in the presence Suitable for use as diluents in the process (A) accordin to the invention are all inert oranic solvents. Preference is iven to usin hydrocarbons, such as toluene and xylene, furthermore ethers, such as dibutyl ether, tetrahydrofuran, dioxane, lycol dimethyl ether and dilycol dimethylether, moreover polar solvents, such as dimethyl sulfoxide, sulfolane, dimethylformamide N-methylpyrrolidone, and also alcohols, such as methanol, ethanol, propanol, isopropanol, butanol,isobutanol and tert-butanol. Suitable bases (deprotonatin aents) for carryin out the process (A) accordin to the invention are all customary proton acceptors. Preference is iven to usin alkali metal and alkaline earth metal oxides, hydroxides and carbonates, such as sodium hydroxide, potassium hydroxide, I manesium oxide, calcium oxide, sodium carbonate, potassium carbonate and calcium carbonate,which can also be used in the presence of phase-transfer catalysts, such as, for example,triethylbenzylammonium chloride, tetrabutylammonium bromide, Adoen 464 (= methyltrialkyl(C-C]o)ammonium chloride) or TDA (= tris(methoxyethoxyethyl)amine). It furthermore possible to use alkali metals, such as sodium or potassium. It is also possible to i employ alkali metal and alkaline earth metal amides and hydrides, such as sodium amide, sodiumhydride and calcium hydride, and additionally also alkali metal alkoxides, such as sodiummethoxide, sodium ethoxide and potassium tert-butoxide. When carryin out the process (A) accordin to the invention, the reaction temperatures can varied within a relatively wide rane. In eneral, the process is carried out at temperatures between20 0°C and 250°C, preferably between 50°C and 50°C. The process (A) accordin to the invention is enerally carried out under atmospheric pressure. When carryin out the process (A) accordin to the invention, the reaction components of the formula (II) and the deprotonatin bases are enerally employed in approximately doubly equimolar amounts. However, it is also possible to use a relatively lare excess (up to 3 mol) 25 one or the other component.The process (B) is characterized in that compounds of the formula (III) in which A, B, , X, Y andR. are as defined above are subected to an intramolecular condensation in the presence of adiluent and in the presence of a base. Suitable for use as diluents in the process (B) accordin to the invention are all inert oranic 30 solvents. Preference is iven to usin hydrocarbons, such as toluene and xylene, furthermore ethers, such as dibutyl ether, tetrahydrofuran, dioxane, lycol dimethyl ether and dilycol dimethylether, moreover polar solvents, such as dimethyl sulfoxide, sulfolane, dimethylformamide and N-methylpyrrolidone, and also alcohols, such as methanol, ethanol, propanol, isopropanol, butanol,isobutanol and tert-butanol. Suitable bases (deprotonatin aents) for carryin out the process (B) accordin to the invention are all customary proton acceptors. Preference is iven to usin alkali metal and alkaline earth metal oxides, hydroxides and carbonates, such as sodium hydroxide, potassium hydroxide, manesium oxide, calcium oxide, sodium carbonate, potassium carbonate and calcium carbonate, which can also be used in the presence of phase-transfer catalysts, such as, for example, triethylbenzylammonium chloride, tetrabutylammonium bromide, Adoen 464 (= methyltrialkyl(C-Ci0)ammonium chloride) or TDA (= tris(methoxyethoxyethyl)amine). It is furthermore possible to use alkali metals, such as sodium or potassium. It is also possible to employ alkali metal and alkaline earth metal amides and hydrides, such as sodium amide, sodium hydride and calcium hydride, and additionally also alkali metal alkoxides, such as sodium methoxide, sodium ethoxide and potassium tert-butoxide. When carryin out the process (B) accordin to the invention, the reaction temperatures can be varied within a relatively wide rane. In eneral, the process is carried out at temperatures between The process (B) accordin to the invention is enerally carried out under atmospheric pressure. When carryin out the process (B) accordin to the invention, the reaction components of the formula (II) and the deprotonatin bases are enerally employed in approximately equimolar amounts. However, it is also possible to use a relatively lare excess (up to 3 mol) of one or the other component.The process (C) is characterized in that compounds of the formula (IV) in which A, B, V, , X, Yand R. are as defined above are cyclized intramolecularly in the presence of an acid and, ifappropriate, in the presence of a diluent. Suitable diluents for the process (C) accordin to the invention are all inert oranic solvents. Preference is iven to usin hydrocarbons, such as toluene and xylene, furthermore haloenated hydrocarbons, such as dichloromethane, chloroform, ethylene chloride, chlorobenzene, dichlorobenzene,moreover polar solvents, such as dimethyl sulfoxide, sulfolane, dimethylformamide andN-methylpyrrolidone. It is furthermore possible to use alcohols, such as methanol, ethanol,propanol, isopropanol, butanol, isobutanol, tert-butanol. If appropriate, the acid used may also serve as diluent.Suitable for use as acid in the process (C) accordin to the invention are all customary inoranicand oranic acids, such as, for example, hydrohalic acids, sulfuric acid, alkyl-, aryl- andhaloalkylsulfonic acids, in particular haloenated alkylcarboxylic acids, such as, for example,trifluoroacetic acid. When carryin out the process (C) accordin to the invention, the reaction temperatures can be varied within a relatively wide rane. In eneral, the process is carried out at temperatures between°C and 250°C, preferably between 50°C and 50°C. The process (C) accordin to the invention is enerally carried out under atmospheric pressure. When carryin out the process (C) accordin to the invention, the reaction components of the formula (IV) and the acid are, for example, employed in equimolar amounts. However, it is alsopossible, if appropriate, to use the acid as solvent or as catalyst. The process (D) accordin to the invention is characterized in that carbonyl compounds of the formula (V) or their enole ethers of the formula (V-a) are reacted with ketene acid halides of theformula (VI) in the presence of a diluent and, if appropriate, in the presence of an acid acceptor.Suitable diluents for use in the process (D) accordin to the invention are all inert oranic solvents.Preference is iven to usin optionally haloenated hydrocarbons, such as toluene, xylene,mesitylene, chlorobenzene and dichlorobenzene, furthermore ethers, such as dibutyl ether, lycoldimethyl ether dilycol dimethyl ether and diphenyl ether, moreover polar solvents, such asdimethyl sulfoxide, sulfolane, dimethylformamide orN-methylpyrrolidone. Suitable acid acceptors for carryin out the process variant (D) accordin to the invention are customary acid acceptors.Preference is iven to usin tertiary amines, such as triethylamine, pyridine, diazabicyclooctane (DABCO), diazabicycloundecane (DBU), diazabicyclononene (DBN), Huni base and N,Ndimethylaniline.When carryin out the process variant (D) accordin to the invention, the reaction temperaturescan be varied within a relatively wide rane. Expediently, the process is carried out at temperaturesbetween 0°C and 250°C, preferably between 50°C and 220°C. The process (D) accordin to the invention is expediently carried out under atmospheric pressure.When carryin out the process (D) accordin to the invention, the reaction components of theformulae (V) and (VI), in which A, D, , X and Y are as defined above and Hal represents haloen,and, if appropriate, the acid acceptors are enerally employed in approximately equimolaramounts. However, it is also possible to use a relatively lare excess (up to 5 mol) of onecomponent or the other.The process (E) accordin to the invention is characterized in that thioamides of the formula (VII)are reacted with ketene acid halides of the formula (VI) in the presence of a diluent and, if appropriate, in the presence of an acid acceptor. Suitable for use as diluents for the process variant (E) accordin to the invention are all inert oranic solvents. Preference is iven to usin hydrocarbons, such as toluene and xylene, furthermore ethers, such as dibutyl ether, lycol dimethyl ether and dilycol dimethyl ether, moreover polar solvents, such as dimethyl sulfoxide, sulfolane, dimethylformamide and Nmethylpyrrolidone.Suitable for use as acid acceptors for carryin out the process (E) accordin to the invention are all customary acid acceptors. Preference is iven to usin tertiary amines, such as triethylamine, pyridine, diazabicyclooctane (DABCO), diazabicycloundecane (DBU), diazabicyclononene (DBN), Hiini base and N,Ndimethylaniline. When carryin out the process (E) accordin to the invention, the reaction temperatures can be varied within a relatively wide rane. Expediently, the process is carried out at temperatures between 0°C and 250°C, preferably between 20°C and 220°C. The process (E) accordin to the invention is expediently carried out under atmospheric pressure.When carryin out the process (E) accordin to the invention, the reaction components of theformulae (VII) and (VI), in which A, , X and Y are as defined above and Hal represents haloen,and, if appropriate, the acid acceptors are enerally employed in approximately equimolaramounts. However, it is also possible to use a relatively lare excess (up to 5 mol) of onecomponent or the other.The process (F) is characterized in that compounds of the formula (VIII) in which A, B, , Q, Q, X, Y and R are as defined above are subected to an intramolecular condensation in the presenceof abase.Suitable diluents for use in the process (F) accordin to the invention are all oranic solventswhich are inert toward the reaction participants. Preference is iven to usin hydrocarbons, toluene and xylene, furthermore ethers, such as dibutyl ether, tetrahydrofuran, dioxane, lycoldimethyl ether and dilycol dimethyl ether, moreover polar solvents, such as dimethyl sulfoxide,sulfolane, dimethylformamide and N-methylpyrrolidone. It is furthermore possible to use alcohols,such as methanol, ethanol, propanol, isopropanol, butanol, isobutanol, tert-butanol.Suitable bases (deprotonatin aents) for carryin out the process (F) accordin to the inventionare all customary proton acceptors. Preference is iven to usin alkali metal and alkaline earthmetal oxides, hydroxides and carbonates, such as sodium hydroxide, potassium hydroxide,manesium oxide, calcium oxide, sodium carbonate, potassium carbonate and calcium carbonate,which can also be used in the presence of phase-transfer catalysts, such as, for example,triethylbenzylammonium chloride, tetrabutylammonium bromide, Adoen 464 (=methyltrialkyl(C-C]0)ammonium chloride) or TDA (= tris(methoxyethoxyethyl)amine). It isfurthermore possible to use alkali metals, such as sodium or potassium. It is also possible toemploy alkali metal and alkaline earth metal amides and hydrides, such as sodium amide, sodiumhydride and calcium hydride, and additionally also alkali metal alkoxides, such as sodium methoxide, sodium ethoxide and potassium tert-butoxide. When carryin out the process (F) accordin to the invention, the reaction temperatures can be varied within a relatively wide rane. In eneral, the process is carried out at temperatures between-75°C and 250°C, preferably between -50°C and 50°C. The process (F) accordin to the invention is enerally carried out under atmospheric pressure. When carryin out the process (F) accordin to the invention, the reaction components of the formula (VIII) and the deprotonatin bases are enerally employed in approximately equimolar amounts. However, it is also possible to use a relatively lare excess (up to 3 mol) of one or theother component.The process () is characterized in that compounds of the formula (IX) in which A, B, Q, Q,Q, Q6, , X, Y and R are as defined above are subected to an intramolecular condensation in presence of bases.Suitable diluents for use in the process () accordin to the invention are all oranic solventswhich are inert toward the reaction participants. Preference is iven to usin hydrocarbons, such astoluene and xylene, furthermore ethers, such as dibutyl ether, tetrahydrofuran, dioxane, lycol dimethyl ether and dilycol dimethyl ether, moreover polar solvents, such as dimethyl sulfoxide, sulfolane, dimethylformamide and N-methylpyrrolidone. It is furthermore possible to use alcohols, such as methanol, ethanol, propanol, isopropanol, butanol, isobutanol, tert-butanol. Suitable bases (deprotonatin aents) for carryin out the process () accordin to the invention are all customary proton acceptors. Preference is iven to usin alkali metal and alkaline earth metal oxides, hydroxides and carbonates, such as sodium hydroxide, potassium hydroxide, manesium oxide, calcium oxide, sodium carbonate, potassium carbonate and calcium carbonate, which can also be used in the presence of phase-transfer catalysts, such as, for example, triethylbenzylammonium chloride, tetrabutylammonium bromide, Adoen 464 (= methyltrialkyl(C-C]0)ammonium chloride) TDA (= tris(methoxyethoxyethyl)amine). It is furthermore possible to use alkali metals, such assodium or potassium. It is also possible to employ alkali metal and alkaline earth metal amides andhydrides, such as sodium amide, sodium hydride and calcium hydride, and additionally also alkalimetal alkoxides, such as sodium methoxide, sodium ethoxide and potassium tert-butoxide.When carryin out the process () accordin to the invention, the reaction temperatures can bevaried within a relatively wide rane. In eneral, the process is carried out at temperatures between0°C and 250°C, preferably between 50°C and 50°C. The process () accordin to the invention is enerally carried out under atmospheric pressure. When carryin out the process () accordin to the invention, the reaction components of the formula (IX) and the deprotonatin bases are enerally employed in approximately equimolar amounts. However, it is also possible to use a relatively lare excess (up to 3 mol) of one or other component.The process (H-a) accordin to the invention is characterized in that hydrazines of the formula (X)or salts of these compounds are reacted with ketene acid halides of the formula (VI) in thepresence of a diluent and, if appropriate, in the presence of an acid acceptor.Suitable diluents for use in the process (H-a) accordin to the invention are all inert oranicsolvents. Preference is iven to usin optionally chlorinated hydrocarbons, such as, for example,mesitylene, chlorobenzene and dichlorobenzene, toluene, xylene, furthermore ethers, such asdibutyl ether, lycol dimethyl ether, dilycol dimethyl ether and diphenylethane, moreover polarsolvents, such as dimethyl sulfoxide, sulfolaiie, dimethylformamide or N-methylpyrrolidone.Suitable acid acceptors for carryin out the process variant (H-a) accordin to the invention Preference is iven to usin tertiary amines, such as triethylamine, pyridine, diazabicyclooctane(DABCO), diazabicycloundecane (DBU), diazabicyclononene (DBN), Hiini base and N,Ndimethylaniline.When carryin out the process variant (H-a) accordin to the invention, the reaction temperaturescan be varied within a relatively wide rane. Expediently, the process is carried out at temperatures between 0°C and 250°C, preferably between 50°C and 220°C. The process (H-a) accordin to the invention is expediently carried out under atmospheric pressure.When carryin out the process (H-a) accordin to the invention, the reaction components of formulae (VI) and (X), in which A, D, , X and Y are as defined above and Hal represents haloen,and, if appropriate, the acid acceptors are enerally employed in approximately equimolaramounts. However, it is also possible to use a relatively lare excess (up to 5 mol) of onecomponent or the other. The process (H-B) is characterized in that hydrazines of the formula (X) or salts of this compound,in which A and D are as defined above, are subected to a condensation with malonic esters ormalonamides of the formula (XI) in which U, , X, Y and R° are as defined above, in the presenceof a base.Suitable diluents for use in the process (H-B) accordin to the invention are all inert oranic solvents. Preference is iven to usin optionally haloenated hydrocarbons, such as toluene, xylene, mesitylene, chlorobenzene and dichlorobenzene, furthermore ethers, such as dibutyl ether, tetrahydrofuran, dioxane, dipheny! ether, lycol dimethyl ether and dilycol dimethyl ether, moreover polar solvents, such as dimethyl sulfoxide, sulfolane, dimethylformamide, dimethylacetamide and N-methylpyrrolidone, and also alcohols, such as methanol, ethanol, propanol, isopropanol, butanol, isobutanol and tert-butanol. Suitable bases (deprotonatin aents) for carryin out the process (H-P) accordin to the invention are all customary proton acceptors. Preference is iven to usin alkali metal and alkaline earth metal oxides, hydroxides and carbonates, such as sodium hydroxide, potassium hydroxide, manesium oxide, calcium oxide, sodium carbonate, potassium carbonate and calcium carbonate, which can also be used in the presence of phase-transfer catalysts, such as, for example, triethylbenzylammonium chloride, tetrabutylammonium bromide, Adoen 464 (= methyltrialkyl(C-C]Q)ammoniurn chloride) or TDA (= tris(methoxyethoxyethyl)amine). It isfurthermore possible to use alkali metals, such as sodium or potassium. It is also possible to employ alkali metal and alkaline earth metal amides and hydrides, such as sodium amide, sodiumhydride and calcium hydride, and additionally also alkali metal alkoxides, such as sodiummethoxide, sodium ethoxide and potassium tert-butoxide. It is also possible to use tertiary amines, such as triethylamine, pyridine, diazabicyclooctane (DABCO), diazabicycloundecane (DBU), diazabicyclononene (DBN), Hiini base and N,Ndimethylaniline.When carryin out the process (H-B) accordin to the invention, the reaction temperatures can bevaried within a relatively wide rane. In eneral, the process is carried out at temperatures between0°C and 20°C, preferably between 50°C and 0°C. The process (H-B) accordin to the invention is enerally carried out under atmospheric pressure.When carryin out the process (H-3) accordin to the invention, the reaction components of theformulae (XI) and (X) are enerally employed in approximately equimolar amounts. However, it isalso possible to use a relatively lare excess (up to 3 mol) of one component or the other.The process (H-y) is characterized in that compounds of the formula (XII) in which A, D, , X, Yand R. are as defined above are subected to an intramolecular condensation in the presence Suitable for use as diluents in the process (H-y) accordin to the invention are all inert oranicolvents. Preference is iven to usin hydrocarbons, such as toluene and xylene, furthermoreethers, such as dibutyl ether, tetrahydrofuran, dioxane, lycol dimethyl ether and dilycol dimethylether, moreover polar solvents, such as dimethyl sulfoxide, sulfolane, dimethylformamide and N-methylpyrrolidone, and also alcohols, such as methanol, ethanol, propanol, isopropanol, butanol,isobutanol and tert-butanol. Suitable bases (deprotonatin aents) for carryin out the process (H-y) accordin to the invention are all customary proton acceptors. Preference is iven to usin alkali metal and alkaline earth metal oxides, hydroxides and carbonates, such as sodium hydroxide, potassium hydroxide, manesium oxide, calcium oxide, sodium carbonate, potassium carbonate and calcium carbonate,which can also be used in the presence of phase-transfer catalysts, such as, for example,triethylbenzylammonium chloride, tetrabutylammonium bromide, Adoen 464 (= methyltrialkyl(C-Ci0)ammoniurn chloride) or TDA (= tris(methoxyethoxyethyl)amine). It isfurthermore possible to use alkali metals, such as sodium or potassium. It is also possible to employ alkali metal and alkaline earth metal amides and hydrides, such as sodium amide, sodiumhydride and calcium hydride, and additionally also alkali metal alkoxides, such as sodiummethoxide, sodium ethoxide and potassium tert-butoxide. When carryin out the process (H-y) accordin to the invention, the reaction temperatures can bevaried within a relatively wide rane. In eneral, the process is carried out at temperatures between0°C and 250°C, preferably between 50°C and 50°C. The process (H-y) accordin to the invention is enerally carried out under atmospheric pressure.When carryin out the process (H-y) accordin to the invention, the reaction components of formula (XII) and the deprotonatin bases are enerally employed in approximately doublyequimolar amounts. However, it is also possible to use a relatively lare excess (up to 3 mol) ofone or the other component. The process (I-a) is characterized in that compounds of the formulae (I-l-a) to (I--a) are in eachcase reacted with carbonyl halides of the formula (XIII), if appropriate in the presence of a diluentand if appropriate in the presence of an acid binder. Suitable diluents for use in the process (I-a) accordin to the invention are all solvents which areinert toward the acid halides. Preference is iven to usin hydrocarbons, such as benzine, benzene,toluene, ylene and tetralin, furthermore haloenated hydrocarbons, such as methylene chloride,chloroform, carbon tetrachloride, chlorobenzene and o-dichlorobenzene, moreover ketones, suchas acetone and methyl isopropyl ketone, furthermore ethers, such as diethyl ether, tetrahydrofuranand dioxane, additionally carboxylic esters, such as ethyl acetate, and also stronly polar solvents,such as dimethyl sulfoxide and sulfolane. The hydrolytic stability of the acid halide permittin, thereaction can also be carried out in the presence of water. Suitable acid binders for the reaction accordin to the process (I-a) accordin to the invention areall customary acid acceptors. Preference is iven to usin tertiary amines, such as triethylamine, pyridine, diazabicyclooctane (DABCO), diazabicycloundecene (DBU), diazabicyclononene (DBN), Hiini base and N,N-dimethylaniline, furthermore alkaline earth metal oxides, such manesium oxide and calcium oxide, moreover alkali metal and alkaline earth metal carbonates, such as sodium carbonate, potassium carbonate and calcium carbonate, and also alkali metal hydroxides, such as sodium hydroxide and potassium hydroxide. The reaction temperatures in the process (I-a) accordin to the invention may be varied within arelatively wide rane. In eneral, the process is carried out at temperatures between -20°C and +50°C, preferably between 0°C and 00°C.When carryin out the process (I-a) accordin to the invention, the startin materials of theformulae (I-l-a) to (I--a) and the carbonyl halide of the formula (XIII) are enerally eachemployed in approximately equivalent amounts. However, it is also possible to use a relatively lare excess (up to 5 mol) of the carbonyl halide. Work-up is carried out by customary methods.The process (I-B) is characterized in that compounds of the formulae (I-l-a) to (I--a) are reactedwith carboxylic anhydrides of the formula (XFV), if appropriate in the presence of a diluent and ifappropriate in the presence of an acid binder. Suitable for use as diluents in the process (I-B) accordin to the invention are, preferably, thosediluents which are also preferred when acid halides are used. Besides, it is also possible for excess to act simultaneously as diluent. Suitable acid binders for process (I-B), which are added, if appropriate, are preferably those acidbinders which are also preferred when acid halides are used. The reaction temperatures in the process (I-B) accordin to the invention can be varied within relatively wide rane. In eneral, the process is carried out at temperatures between -20°C and +50°C, preferably between 0°C and 00°C. When carryin out the process (I-B) accordin to the invention, the startin materials of the formulae (I-l-a) to (I--a) and the carboxylic anhydride of the formula (XIV) are enerally each employed in approximately equivalent amounts. However, it is also possible to use a relativelylare excess (up to 5 mol) of the carboxylic anhydride. Work-up is carried out by customarymethods. In eneral, diluent and excess carboxylic anhydride and the carboxylic acid formed are removed by distillation or by washin with an oranic solvent or with water. The process () is characterized in that compounds of the formulae (I-l-a) to (I-a) are in each case reacted with chloroformic esters or chloroformic thioesters of the formula (XV), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder. Suitable acid binders for the reaction accordin to process () accordin to the invention are all customary acid acceptors. Preference is iven to usin tertiary amines, such as triethylamine, pyridine, DABCO, DBU, DBA, Hiini base and N,N-dimethylaniline, furthermore alkaline earth metal oxides, such as manesium oxide'and calcium oxide, moreover alkali metal and alkaline earth metal carbonates, such as sodium carbonate, potassium carbonate and calcium carbonate, and also alkali metal hydroxides, such as sodium hydroxide and potassium hydroxide. Suitable diluents for use in the process () accordin to the invention are all solvents which are inert toward the chloroformic esters or chloroformic thioesters. Preference is iven to usin hydrocarbons, such as benzine, benzene, toluene, xylene and tetralin, furthermore haloenated hydrocarbons, such as methylene chloride, chloroform, carbon tetrachloride, chlorobenzene and odichlorobenzene, moreover ketones, such as acetone and methyl isopropyl ketone, furthermore ethers, such as diethyl ether, tetrahydrofuran and dioxane, additionally carboxylic esters, such as ethyl acetate, and also stronly polar solvents, such as dimethyl sulfoxide and sulfolane. When carryin out the process () accordin to the invention, the reaction temperatures can be varied within a relatively wide rane, If the reaction is carried out in the presence of a diluent and an acid binder, reaction temperatures are enerally between -20°C and +00°C, preferably between 0°C and 50°C. The process () accordin to the invention is enerally carried out under atmospheric pressure. When carryin out the process () accordin to the invention, the startin materials of the formulae (I-l-a) to (I--a) and the appropriate chloroformic ester or chloroformic thioester of the formula (XIII) are enerally each employed in approximately equivalent amounts. However, it is also possible to use a relatively lare excess (up to 2 mol) of one component or the other. Work-up is carried out by customary methods. In eneral, precipitated salts are removed and the reaction mixture that remains is concentrated by removin the diluent under reduced pressure. The process (K) accordin to the invention is characterized in that compounds of the formulae (I- -a) to (I--a) are in each case reacted with compounds of the formula (XVI) in the presence of a diluent and, if appropriate, in the presence of an acid binder. In preparation process (K), about mol of chloromonothioformic ester or chlorodithioformic ester of the formula (XVI) is reacted per mole of the startin material of the formulae (I-l-a) to (I--a) at from 0 to 20°C, preferably from 20 to 60°C. Suitable diluents, which are added, if appropriate, are all inert polar oranic solvents, such as ethers, amides, sulfones, sulfoxides, and also haloenated alkanes. Preference is iven to usin dimethyl sulfoxide, tetrahydrofuran, dimethylformamide or methylene chloride. If, in a preferred embodiment, the enolate salt of the compounds (I-l-a) to (I--a) is prepared by addition of stron deprotonatin aents, such as, for example, sodium hydride or potassium tertbutoxide, the further addition of acid 20- If acid binders are used, customary inoranic or oranic bases are suitable, by way of example sodium hydroxide, sodium carbonate, potassium carbonate, pyridine, triethylamine. The reaction can be carried out at atmospheric pressure or under elevated pressure and is preferably carried out at atmospheric pressure. Work-up is carried out by customary methods. The process (L) accordin to the invention is characterized in that compounds of the formulae (-- a) to (I--a) are in each case reacted with sulfonyl chlorides of the formula (XVII), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder. In preparation process (L), about mol of sulfonyl chloride of the formula (XVII) is reacted per mole of startin material of the formula (I-l-a to I--a), at from -20 to 50°C, preferably from 20 to 70°C. Suitable diluents, which are added, if appropriate, are all inert polar oranic solvents, such as ethers, amides, nitriles, sulfones, sulfoxides or haloenated hydrocarbons, such as methylene chloride. Preference is iven to usin dimethyl sulfoxide, tetrahydrofuran, dimethylformamide, methylene chloride. If, in a preferred embodiment, the enolate salt of the compounds (I-l-a) to (I--a) is prepared by addition of stron deprotonatin aents (such as, for example, sodium hydride or potassium tertbutoxide), the further addition of acid binders may be dispensed with. If acid binders are used, customary inoranic or oranic bases are suitable, by way of example sodium hydroxide, sodium carbonate, potassium carbonate, pyridine, triethylamine. The reaction can be carried out at atmospheric pressure or under elevated pressure and is preferably carried out at atmospheric pressure. Work-up is carried out by customary methods. The process (M) accordin to the invention is characterized in that compounds of the formulae (I- -a) to (I--a) are in each case reacted with phosphorus compounds of the formula (XVIII), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder. In preparation process (M), to obtain compounds of the formulae (I-l-e) to (I--e) to 2, preferably to .3, mol of the phosphorus compound of the formula (XVIII) are employed per mole of the compounds (I-l-e) to (I--e), at temperatures between -40°C and 50°C, preferably between-0 and 0°C. Suitable diluents which are added, if appropriate, are all inert polar oranic solvents, such as ethers, amides, nitriles, alcohols, sulfides, sulfones, sulfoxides, etc. Preference is iven to usin acetonitrile, dimethyl sulfoxide, tetrahydrofuran, dimethylformamide, methylene chloride. Suitable acid binders, which are added, if appropriate, are customary inoranic or oranic bases, such as hydroxides, carbonates or amines. Sodium hydroxide, sodium carbonate, potassium carbonate, pyridine, triethylamine may be mentioned by way of example. The reaction can be carried out at atmospheric pressure or under elevated pressure and is preferably carried out at atmospheric pressure. Work-up is carried out by customary methods of oranic chemistry. The end products obtained are preferably purified by crystallization, chromatoraphic purification or by so-called "incipient distillation", i.e. removal of the volatile components under reduced pressure. The process (N) is characterized in that compounds of the formulae (I-l-a) to (I--a) are reacted with metal hydroxides or metal alkoxides of the formula (XIX) or amines of the formula (XX), if appropriate in the presence of a diluent. Suitable for use as diluents in the process (N) accordin to the invention are, preferably, ethers, such as tetrahydrofuran, dioxane, diethyl ether, or else alcohols, such as methanol, ethanol, isopropanol, but also water. The process (N) accordin to the invention is enerally carried out under atmospheric pressure. The reaction temperatures are enerally between -20°C and 00°C, preferably between 0°C accordin to the invention is characterized in that compounds of the formulae (I- -a) to (I--a) are in each case reacted with (O-a) compounds of the formula (XXI), if appropriate in the presence of a diluent and if appropriate in the presence of a catalyst, or (O-I3) with compounds of the formula (XXII), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder. In preparation process (O-a), about mol of isocyanate of the formula (XXI) is employed per mole of startin material of the formulae (I-l-a) to (I--a), at from 0 to 00°C, preferably Suitable diluents, which are added, if appropriate, are all inert oranic solvents, such as ethers, amides, nitriles, sulfones, sulfoxides. If appropriate, catalysts may be added to accelerate the reaction. Suitable for use as catalysts are, very advantaeously, oranotin compounds, such as, for example, dibutyltin dilaurate. The reaction is preferably carried out at atmospheric pressure. In preparation process (O-B), about mol of carbamoyl chloride of the formula (XXII) is employed per mole of startin material of the formulae (I-l-a) to (I--a) at from -20 to 50°C, preferably from 0 to 70°C. Suitable diluents, which are added, if appropriate, are all inert polar oranic solvents, such as ethers, amides, sulfones, sulfoxides or haloenated hydrocarbons. Preference is iven to usin dimethyl sulfoxide, tetrahydrofuran, dimethylformamide or methylene chloride. If, in a preferred embodiment, the enolate salt of the compound (I-l-a) to (I--a) is prepared by addition of stron deprotonatin aents (such as, for example, sodium hydride or potassium tertbutoxide), the further addition of acid binders may be dispensed with. If acid binders are used, customary inoranic or oranic bases are suitable, by way of example sodium hydroxide, sodium carbonate, potassium carbonate, triethylamine or pyridine. The reaction may be carried out at atmospheric pressure or under elevated pressure and is preferably carried out at atmospheric pressure. Work-up is carried out by customary methods. The process (Pa) is characterized in that compounds of the formulae (I-l-a) to (I--a) in which defined above and W preferably represents bromine are reacted with metal iodides (for example sodium iodide, potassium iodide), if appropriate in the presence of a base and a Cu(I) salt (for example CuBr or Cul). Suitable for use as diluents in the process (Pa) accordin to the invention are all oranic solvents which are inert toward the reaction participants. Preference is iven to usin hydrocarbons, such toluene and xylene, furthermore ethers, such as dibutyl ether, tetrahydrofuran, dioxane, lycol dimethyl ether and dilycol dimethyl ether, moreover polar solvents, such as dimethyl sulfoxide, sulfolane, dimethylformamide, dimethylacetamide and N-methylpyrrolidone, esters, such as methyl acetate, ethyl acetate, propyl acetate, and also alcohols, such as, for example, methanol, ethanol, propanol, isopropanol, butanol and isobutanol. Suitable bases for carryin out the process (Pa) accordin to the invention are especially oranic bases. Preference is iven to usin amines, such as, for example, N,N-dimethylethylenediamine, ,2- diaminocyclohexane. When carryin out the process (Pa) accordin to the invention, the reaction temperature can be varied within a relatively wide rane. In eneral, the process is carried out at temperatures between 0°C and 250°C, preferably between 50°C and 50°C. The process (Pa) accordin to the invention is enerally carried out under atmospheric pressure. When carryin out the process (Pa) accordin to the invention, the reaction component of the formula (I-l-a) to (I--a') is enerally reacted with excesses of the metal iodides of up to 20 mol, preferably from . to 5 mol. The copper(I) salts are enerally employed in catalytic amounts; from 0.00 to 0.5 mol, preferably from 0.0 to 0.2 mol. However, they can also be employed in equimolar amounts. The process (Pli) is characterized in that compounds of the formulae (I-l-a) to (I--a) in which A, B, s defined above and W preferably represents bromine are subected to a haloen/metal exchane with metal oranyls and the anion formed is reacted with iodinatin aents. Suitable diluents for use in the process (PB) accordin to the invention are all oranic solvents which are inert toward the reaction participants. Preference is iven to usin hydrocarbons, such as toluene and xylene, furthermore ethers, such as diethyl ether, methyl tert-butyl ether, dibutyl ether, tetrahydrofuran, dioxane, lycol dimethyl ether and dilycol dimethyl ether. Suitable for use as iodinatin aents for carryin out the process (PB) are customary reaents, such as iodine, iodine monochloride, iodine monobromide. When carryin out the process (PB) accordin to the invention, all customary metal oranyls can be used for the haloen/metal exchane. Preference is iven to usin n-butyllithium, sec-butyllithium, tert-butyllithium, phenyllithium. When carryin out the process (PB) accordin to the invention, the reaction temperature can be varied within a relatively wide rane. In eneral, the process is carried out at temperatures between -20°C and 50°C, preferably between -7°C and 30°C. The process (PB) accordin to the invention is enerally carried out under atmospheric pressure. When carryin out the process (PB) accordin to the invention, the reaction component of the formula (I-l-a) to (I--a) is enerally reacted with excesses of the metal oranyls and the iodinatin aents of up to 20 mol, preferably from .2 to 5 mol. The inventive active compounds/active compound combinations, in combination with ood plant tolerance and favourable toxicity to warm-blooded animals and bein tolerated well by the environment, are suitable for protectin plants and plant orans, for increasin the harvest yields, for improvin the quality of the harvested material and for controllin animal pests, in particular insects, arachnids, helminths, nematodes and molluscs, which are encountered in ariculture, in horticulture, in animal husbandry, in forests, in ardens and leisure facilities, in the protection of stored products and of materials, and in the hyiene sector. They may be preferably employed as plant protection aents. They are active aainst normally sensitive and resistant species and aainst all or some staes of development. The abovementioned pests include: From the order of the Anoplura (Phthiraptera), for example, Damalinia spp., Haematopinus spp., Linonathus spp., Pediculus spp., Trichodectes spp. From the class of the Arachnida, for example, Acarus siro, Aceria sheldoni, Aculops spp., Aculus spp., Amblyomma spp., Aras spp., Boophilus spp., Brevipalpus spp., Bryobia praetiosa, Chorioptes spp., Dermanyssus allinae, Eotetranychus spp., Epitrimerus pyri, Eutetranychus spp., Eriophyes spp., Hemitarsonemus spp., Hyalomma spp., Ixodes spp., Latrodectus mactans, Metatetranychus spp., Olionychus spp., Ornithodoros spp., Panonychus spp., Phyllocoptruta oleivora, Polyphaotarsonemus latus, Psoroptes spp., Rhipicephalus spp., Rhizolyphus spp., Sarcoptes spp., Scorpio maurus, Stenotarsonemus spp., Tarsonemus spp., Tetranychus spp., Vasates lycopersici. From the class of the Bivalva, for example, Dreissena spp. From the order of the Chilopoda, for example, eophilus spp., Scutiera spp. From the order of the Coleoptera, for example, Acanthoscelides obtectus, Adoretus spp., Aelastica alni, Ariotes spp., Amphimallon solstitialis, Anobium punctatum, Anoplophora spp., Anthonomus spp., Anthrenus spp., Apoonia spp., Atomaria spp., Attaenus spp., Bruchidius obtectus, Bruchus spp., Ceuthorhynchus spp., Cleonus mendicus, Conoderus spp., Cosmopolites spp., Costelytra zealandica, Curculio spp., Cryptorhynchus lapathi, Dermestes spp., Diabrotica spp., Epilachna spp., Faustinus cubae, ibbium psylloides, Heteronychus arator, Hylamorpha eleans, Hylotrupes baulus, Hypera postica, Hypothenemus spp., Lachnosterna consanuinea, Leptinotarsa decemlineata, Lissorhoptrus oryzophilus, Lixus spp., Lyctus spp., Meliethes aeneus, Melolontha melolontha, Midolus spp., Monochamus spp., Naupactus xanthoraphus, Niptus hololeucus, Oryctes rhinoceros, Oryzaephilus surinamensis, Otiorrhynchus sulcatus, Oxycetonia ucunda, Phaedon cochleariae, Phyllophaa spp., Popillia aponica, Premnotrypes spp., Psylliodes chrysocephala, Ptinus spp., Rhizobius ventralis, Rhizopertha dominica, Sitophilus spp., Sphenophorus spp., Sternechus .spp., Symphyletes spp., Tenebrio molitor, Tribolium spp., Trooderma spp., Tychius spp., Xylotrechus spp., Zabrus spp. From the order of the Collembola, for example, Onychiurus armatus. From the order of the Dermaptera, for example, Forficula auricularia. From the order of the Diplopoda, for example, Blaniulus uttulatus. From the order of the Diptera, for example, Aedes spp., Anopheles spp., Bibio hortulanus, Calliphora erythrocephala, Ceratitis capitata, Chrysomyia spp., Cochliomyia spp., Cordylobia anthropophaa, Culex spp., Cuterebra spp., Dacus oleae, Dermatobia hominis, Drosophila spp., Fannia spp., astrophilus spp., Hylemyia spp., Hyppobosca spp., Hypoderma spp., Liriomyza spp., Lucilia spp., Musca spp., Nezara spp., Oestrus spp., Oscinella frit, Peomyia hyoscyami, Phorbia spp., Stomoxys spp., Tabanus spp., Tannia spp., Tipula paludosa. From the class of the astropoda, for example, Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., alba spp., Lymnaea spp., Oncomelania spp., Succinea spp. From the class of the helminths, for example, Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Bruia malayi, Bruia timori, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp., Dicrocoelium spp, Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus medinensis, Echinococcus ranulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp., Heterakis spp., Hymenolepis nana, Hyostronulus spp., Loa Loa, Nematodirus spp., Oesophaostomum spp., Opisthorchis spp., Onchocerca volvulus, Ostertaia spp., Paraonimus spp., Schistosomen spp, Stronyloides fuelleborni, Stronyloides stercoralis, Stronyloides spp., Taenia sainata, Taenia solium, Trichinella spiralis, Trichinella nativa, Trichinella britovi, Trichinella nelsoni, Trichinella pseudopsiralis, Trichostronulus spp., Trichuris trichuria, Wuchereria bancrofti. It is furthermore possible to control Protozoa, such as Eimeria. From the order of the Heteroptera, for example, Anasa tristis, Antestiopsis spp., Blissus spp., Calocoris spp., Campylomma livida, Cavelerius spp., Cimex spp., Creontiades dilutus, Dasynus piperis, Dichelops furcatus, Diconocoris hewerti, Dysdercus spp., Euschistus spp., Euryaster spp., Heliopeltis spp., Horcias nobilellus, Leptocorisa spp., Leptolossus phyllopus, Lyus spp., Macropes excavatus, Miridae, Nezara spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., Psallus seriatus, Pseudacysta persea, Rhodnius spp., Sahlberella sinularis, Scotinophora spp., Stephanitis nashi, Tibraca spp., Triatoma spp. From the order of the Homoptera, for example, Acyrthosipon spp., Aeneolamia spp., Aonoscena spp., Aleurodes spp., Aleurolobus barodensis, Aleurothrixus spp., Amrasca spp., Anuraphis cardui, Aonidiella spp., Aphanostima piri, Aphis spp., Arboridia apicalis, Aspidiella spp., Aspidiotus spp., Atanus spp., Aulacorthum solani, Bemisia spp., Brachycaudus helichrysii, Brachycolus spp., Brevicoryne brassicae, Calliypona marinata, Carneocephala fulida, Ceratovacuna laniera, Cercopidae, Ceroplastes spp., Chaetosiphon fraaefolii, Chionaspis tealensis, Chlorita onukii, Chromaphis ulandicola, Chrysomphalus ficus, Cicadulina mbila, Coccomytilus halli, Coccus spp., Cryptomyzus ribis, Dalbulus spp., Dialeurodes spp., Diaphorina spp., Diaspis spp., Drosicha spp., Dysaphis spp., Dysmicoccus spp., Empoasca spp., Eriosoma spp., Erythroneura spp., Euscelis bilobatus, eococcus coffeae, Homalodisca coaulata, Hyalopterus arundinis, Icerya spp., Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., Lepidosaphes spp., Lipaphis erysimi, Macrosiphum spp., Mahanarva fimbriolata, Melanaphis sacchari, Metcalfiella spp., Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzus spp., Nasonovia ribisniri, Nephotettix spp., Nilaparvata luens, Oncometopia spp., Orthezia praelona, Parabemisia myricae, Paratrioza spp., Parlatoria spp., Pemphius spp., Pererinus maidis, Phenacoccus spp., Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp., Pinnaspis aspidistrae, Planococcus spp., Protopulvinaria pyriformis, Pseudaulacaspis pentaona, Pseudococcus spp., Psylla spp., Pteromalus spp., Pyrilla spp., Quadraspidiotus spp., Quesada ias, Rastrococcus spp., Rhopalosiphum spp., Saissetia spp., Scaphoides titanus, Schizaphis raminum, Selenaspidus articulatus, Soata spp., Soatella furcifera, Soatodes spp., Stictocephala festina, Tenalaphara malayensis, Tinocallis caryaefoliae, Tomaspis spp., Toxoptera spp., Trialeurodes vaporariorum, Trioza spp., Typhlocyba spp., Unaspis spp., Viteus vitifolii. From the order of the Hymenoptera, for example, Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Vespa spp. From the order of the Isopoda, for example, Armadillidium vulare, Oniscus asellus, Porcellio scaber. From the order of the Isoptera, for example, Reticulitermes spp. From the order of the Lepidoptera, for example, Acronicta maor, Aedia leucomelas, Arotis spp., Alabama arillacea, Anticarsia spp., Barathra brassicae, Bucculatrix thurberiella, Bupalus piniarius, Cacoecia podana, Capua reticulana, Carpocapsa pomonella, Cheimatobia brumata, Chilo spp., Choristoneura fumiferana, Clysia ambiuella, Cnaphalocerus spp., Earias insulana, Ephestia kuehniella, Euproctis chrysorrhoea, Euxoa spp., Feltia spp., alleria mellonella, Helicoverpa spp., Heliothis spp., Hofmannophila pseudospretella, Homona mananima, Hyponomeuta padella, Laphyma spp., Lithocolletis blancardella, Lithophane antennata, Loxarotis albicosta, Lymantria spp., Malacosoma neustria, Mamestra brassicae, Mocis repanda, Mythimna separata, Oria spp., Oulema oryzae, Panolis flammea, Pectinophora ossypiella, Phyllocnistis citrella, Pieris spp., Plutella xylostella, Prodenia spp., Pseudaletia spp., Pseudoplusia includens, Pyrausta nubilalis, Spodoptera spp., Thermesia emmatalis, Tinea pellionella, Tineola bisselliella, Tortrix viridana, Trichoplusia spp. From the order of the Orthoptera, for example, Acheta domesticus, Blatta orientalis, Blattella ermanica, ryllotalpa spp., Leucophaea maderae, Locusta spp., Melanoplus spp., Periplaneta americana, Schistocerca rearia. From the order of the Siphonaptera, for example, Ceratophyllus spp., Xenopsylla cheopis. From the order of the Symphyla, for example, Scutierella immaculata. From the order of the Thysanoptera, for example, Baliothrips biformis, Enneothrips flavens, Frankliniella spp., Heliothrips spp., Hercinothrips femoralis, Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamoni, Thrips spp. From the order of the Thysanura, for example, Lepisfna saccharina. The phytoparasitic nematodes include, for example, Aphelenchoides spp., Bursaphelenchus spp., Dirylenchus dipsaci, lobodera spp., Heterodera spp., Lonidorus spp., Meloidoyne spp., Pratylenchus spp., Radopholus similis, Trichodorus spp., Tylenchulus semipenetrans, Xiphinema spp. If appropriate, the compounds/active compound combinations accordin to the invention can, at certain concentrations or application rates, also be used as herbicides, safeners, rowth reulators or aents to improve plant properties, or as microbicides, for example as funicides, antimycotics, bactericides, viricides (includin aents aainst viroids) or as aents aainst MLO (Mycoplasmalike oranisms) and RLO (Rickettsia-like oranisms). If appropriate, they can also be employed as intermediates or precursors for the synthesis of other active compounds. All plants and plant parts can be treated in accordance with the invention. Plants are to be understood as meanin in the present context all plants and plant populations such as desired and undesired wild plants or crop plants (includin naturally occurrin crop plants). Crop plants can be plants which can be obtained by conventional plant breedin and optimization methods or by biotechnoloical and enetic enineerin methods or by combinations of these methods, includin the transenic plants and includin the plant cultivars protectable or not protectable by plant breeders' rihts. Plant parts are to be understood as meanin all parts and orans of plants above and below the round, such as shoot, leaf, flower and root, examples which may be mentioned bein leaves, needles, stalks, stems, flowers, fruit bodies, fruits, seeds, roots, tubers and rhizomes. The plant parts also include harvested material, and veetative and enerative propaation material, for example cuttins, tubers, rhizomes, offshoots and seeds. Treatment accordin to the invention of the plants and plant parts with the active compounds/active compound combinations is carried out directly or by allowin the compounds to act on their surroundins, habitat or storae space by the customary treatment methods, for example by immersion, sprayin, evaporation, foin, scatterin, paintin on, inection and, in the case of propaation material, in particular in the case of seeds, also by applyin one or more coats. The active compounds/active compound combinations can be converted to the customary formulations, such as solutions, emulsions, wettable powders, water- and oil-based suspensions, powders, dusts, pastes, soluble powders, soluble ranules, ranules for broadcastin, suspensionemulsion concentrates, natural materials imprenated with active compound, synthetic materials imprenated with active compound, fertilizers and microencapsulations in polymeric substances. These formulations are produced in a known manner, for example by mixin the active compounds/active compound combinations with extenders, that is liquid solvents and/or solid carriers, optionally with the use of surfactants, that is emulsifiers and/or dispersants and/or foamformers. If the extender used is water, it is also possible to use oranic solvents, for example, as auxiliary solvents. Suitable liquid solvents are esentially aromatics, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and veetable oils, alcohols, such as butanol or lycol, as well as their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, stronly polar solvents, such as dimethyl sulfoxide, and also water. -30- Suitable solid carriers are: for example ammonium salts and round natural minerals such as kaolins, clays, talc, chalk, quartz, attapulite, montmorillonite or diatomaceous earth, and round synthetic minerals such as hihly disperse silica, alumina and silicates; suitable solid carriers for ranules are: for example crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, or else synthetic ranules of inoranic and oranic meals, and ranules of oranic material such as sawdust, coconut shells, maize cobs and tobacco stalks; suitable emulsifiers and/or foam formers are: for example nonionic and anionic emulsifiers such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polylycol ethers, alkylsulphonates, alkyl sulfates, arylsulfonates, or else protein hydrolyzates; suitable dispersants are: for example linosulfite waste liquors and methylcellulose. Tackifiers such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, ranules or latices, such as um arabic, polyvinyl alcohol and polyvinyl acetate, or else natural phospholipids such as cephalins and lecithins and synthetic phospholipids can be used in the formulations. Other additives can be mineral and veetable oils. It is possible to use colorants such as inoranic piments, for example iron oxide, titanium oxide and Prussian blue, and oranic colorants such as alizarin colorants, azo colorants and metal phthalocyanine colorants, and trace nutrients such as salts of iron, mananese, boron, copper, cobalt, molybdenum and zinc. The formulations enerally comprise between 0. and 95% by weiht of active compound, preferably between 0.5 and 90%. The active compound/active compound combinations accordin to the invention can be present in their commercially available formulations, as well as in the use forms prepared from these formulations, in a mixture with other active compounds such as insecticides, attractants, sterilizers, bactericides, acaricides, nematicides, funicides, rowth-reulatin substances, herbicides, safeners, fertilizers or semiochemicals. Compounds which are suitable as mixin partners are, for example, the followin: Funicides: 2-phenylphenol; -hydroxyquinoline sulfate; acibenzolar-S-methyl; aldimorph; amidoflumet; ampropylfos; ampropylfos-potassium; andoprim; anilazine; azaconazole; azoxystrobin; benalaxyl; benodanil; benomyl; benthiavalicarb-isopropyl; benzamacril; benzamacril-isobutyl; bilanafos; -3 - binapacryl; biphenyl; bitertanol; blasticidin-S; bromuconazole; bupirimate; buthiobate; butylamine; calcium polysulfide; capsimycin; captafol; captan; carbendazim; carboxin; carpropamid; carvone; chinomethionat; chlobenthiazone; chlorfenazole; chloroneb; chlorothalonil; chlozolinate; clozylacon; cyazofamid; cyflufenamid; cymoxanil; cyproconazole; cyprodinil; cyprofuram; Daer ; debacarb; dichlofluanid; dichlone; dichlorophen; diclocymet; diclomezine; dicloran; diethofencarb; difenoconazole; diflumetorim; dimethirimol; dimethomorph; dimoxystrobin; diniconazole; dinconazole-M; dinocap; diphenylamine; dipyrithione; ditalimfos; dithianon; dodine; drazoxolon; edifenphos; epoxiconazole; ethaboxam; ethirimol; etridiazole; famoxadone; fenamidone; fenapanil; fenarimol; fenbuconazole; fenfuram; fenhexamid; fenitropan; fenoxanil; fenpiclonil; fenpropidin; fenpropimorph; ferbam; fluazinam; flubenzimine; fludioxonil; flumetover; flumorph; fluoromide; fluoxastrobin; fluquinconazole; flurprimidol; flusilazole; flusulfamide; flutolanil; flutriafol; folpet; fosetyl-Al; fosetyl-sodium; fuberidazole; furalaxyl; furametpyr; furcarbanil; furmecyclox; uazatine; hexachlorobenzene; hexaconazole; hymexazole; imazalil; imibenconazole; iminoctadine triacetate; iminoctadine tris(albesilate); iodocarb; ipconazole; iprobenfos; iprodione; iprovalicarb; irumamycin; isoprothiolane; isovaledione; kasuamycin; kresoxim-methyl; maricozeb; maneb; meferimzone; mepanipyrim; mepronil; metalaxyl; metalaxyl-M; metconazole; methasulfocarb; methfuroxam; metiram; metominostrobin; metsulfovax; mildiomycin; myclobutanil; myclozolin; natamycin; nicobifen; nitrothal-isopropyl; noviflumuron; nuarimol; ofurace; orysastrobin; oxadixyl; oxolinic acid; oxpoconazole; oxycarboxin; oxyfenthiin; paclobutrazole; pefurazoate; penconazole; pencycuron; phosdiphen; phthalide; picoxystrobin; piperalin; polyoxins; polyoxorim; probenazole; prochloraz; procymidone; propamocarb; propanosine-sodiurri; propiconazole; propineb; proquinazid; prothioconazole; pyraclostrobin; pyrazophos; pyrifenox; pyrimethanil; pyroquilon; pyroxyfur; pyrrolenitrine; quinconazole; quinoxyfen; quintozene; simeconazole; spiroxamine; sulfur; tebuconazole; tecloftalam; tecnazene; tetcyclacis; tetraconazole; thiabendazole; thicyofen; thifluzamide; thiophanate-methyl; thiram; tioxymid; tolclofos-methyl; tolylfluanid; triadimefon; triadimenol; triazbutil; triazoxide; tricyclamide; tricyclazole; tridemorph; trifloxystrobin; triflumizole; triforine; triticonazole; uniconazole; validamycin A; vinclozolin; zineb; ziram; zoxamide; (2S)-N-[2-[4-[[3-(4-chlorophenyl)-2-propynyl]oxy]-3-methoxyphenyl]ethyl]-3-methyl- 2-[(methylsulfonyl)amino]butanamide; l-(l-naphthalenyl)-lH-pyrrole-2,5-dione; 2,3,5,6- tetrachloro-4-(methylsulfonyl)pyridine; 2-amino-4-methyl-N-phenyl-5-thiazolecarboxamide; chloro-N-(2,3-dihydro-l,l,3-trimethyl-lH-inden-4-yl)-3-pyridinecarboxamide; 3,4,5-trichloro-2,6- pyridinedicarbonitrile; actinovate; cis-l-(4-chlorophenyl)-2-(lH-l,2,4-triazol-l-yl)cycloheptanol; methyl l-(2,3-dihydro-2,2-dimethyl-lH-inden-l-yl)-lH-imidazole-5-carboxylate; monopotassium carbonate; N-(6-methoxy-3-pyridinyl)cyclopropanecarboxamide; N-butyl--( , -dimethylethyl)- - oxaspiro[4.5]decane-3-amine; sodium tetrathiocarbonate; and copper salts and preparations, such as Bordeaux mixture; copper hydroxide; copper naphthenate; copper oxychloride; copper sulfate; cufraneb; cuprous oxide; mancopper; oxine-copper. Bactericides: bronopol, dichlorophen, nitrapyrin, nickel dimethyldithiocarbamate, kasuamycin, octhilinone, furancarboxylic acid, oxytetracyclin, probenazole, streptomycin, tecloftalam, copper sulfate and other copper preparations. Insecticides/acaricides/nematicides: . Acetylcholine esterase (AChE) inhibitors . Carbamates, for example alanycarb, aldicarb, aldoxycarb, allyxycarb, aminocarb, bendiocarb, benfuracarb, bufencarb, butacarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, cloethocarb, dimetilan, ethiofencarb, fenobucarb, fenothiocarb, formetanate, furathiocarb, isoprocarb, metam-sodium, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, promecarb, propoxur, thiodicarb, thiofanox, trimethacarb, XMC, xylylcarb, triazamate .2 Oranophosphates, for example acephate, azamethiphos, azinphos (-methyl, -ethyl), bromophos-ethyl, bromfenvinfos (-methyl), butathiofos, cadusafos, carbophenothion, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos (-methyl/-ethyl), coumaphos, cyanofenphos, cyanophos, chlorfenvinphos, demeton-S-methyl, demeton-S-methyl sulfone, dialifos, diazinon, dichlofenthion, dichlorvos/DDVP, dicrotophos, dimethoate, dimethylvinphos, dioxabenzofos, disulfoton, EPN, ethion, ethoprophos, etrimfos, famphur, fenamiphos, fenitrothion, fensulfothion, fenthion, flupyrazofos, fonofos, formothion, fosmethilan, fosthiazate, heptenophos, iodofenphos, iprobenfos, isazofos, isofenphos, isopropyl O-salicylate, isoxathion, malathion, mecarbam, methacrifos, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion (-methyl/-ethyl), phenthoate, phorate, phosalone, phosmet, phosphamidon, phosphocarb, phoxim, pirimiphos (-methyl/-ethyl), profenofos, propaphos, propetamphos, prothiofos, prothoate, pyraclofos, pyridaphenthion, pyridathion, quinalphos, sebufos, sulfotep, sulprofos, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, triclorfon, vamidothion -33- 2. Sodium channel modulators / voltae-ated sodium channel blockers 2. Pyrethroids, for example acrinathrin, allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, bioallethrin, bioallethrin-S cyclopentyl isomer, bioethanomethrin, biopermethrin, bioresmethrin, chlovaporthrin, cis-cypermethrin, cis-resmethrin, cis-permethrin, clocythrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin (alpha-, beta-, theta-, zeta-), cyphenothrin, deltamethrin, empenthrin (IR isomer), esfenvalerate, etofenprox, fenfluthrin, fenpropathrin, fenpyrithrin, fenvalerate, flubrocythrinate, flucythrinate, flufenprox, flumethrin, fluvalinate, fubfenprox, amma-cyhalothrin, imiprothrin, kadethrin, lambda-cyhalothrin, metofluthrin, permethrin (cis-, trans-), phenothrin (IR trans-isomer), prallethrin, profluthrin, protrifenbute, pyresmethrin, resmethrin, RU 5525, silafluofen, tau-fluvalinate, tefluthrin, terallethrin, tetramethrin (IR isomer), tralomethrin, transfluthrin, ZXI 90, pyrethrins (pyrethrum) for example acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazine, thiacloprid, thiamethoxam 3.2 Nicotine, bensultap, cartap Acetylcholine receptor modulators 4. Spinosyns, for example spinosad ABA-ated chloride channel antaonists 5. Cyclodiene oranochlorines, for example camphechlor, chlordane, endosulfan, amma-HCH, HCH, heptachlor, lindane, methoxychlor -34- 5.2 Fiproles, for example acetoprole, ethiprole, fipronil, pyrafluprole, pyripole, vaniliprole Chloride channel activators 6. Mectins, for example avermectin, emamectin, emamectin benzoate, ivermectin, milbemycin uvenile hormone mimetics, for example diofenolan, epofenonane, fenoxycarb, hydroprene, kinoprene, methoprene, pyriproxifen, triprene Ecdyson aonists/disruptors . Diacylhydrazines, for example chromafenozide, halofenozide, methoxyfenozide, tebufenozide Chitin biosynthesis inhibitors 9. Benzoylureas, for example bistrifluron, chlofluazuron, diflubenzuron, fluazuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron, triflumuron 9.2 Buprofezin 9.3 Cyromazine Oxidative phosphorylation inhibitors, ATP disrupters 0. Diafenthiuron 0.2 Oranotins, for example azocyclotin, cyhexatin, fenbutatin oxide Oxidative phosphorylation decouplers actin by interruptin the H-proton radient . Pyrroles, for example chlorfenapyr -35- .2 Dinitrophenols, for example binapacyrl, dinobuton, dinocap, DNOC Pae-I electron transport inhibitors 2. METIs, for example fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad, tolfenpyrad 2.2 Hydramethylnone 2.3 Dicofol Pae-II electron transport inhibitors Rotenone Pae-Ill electron transport inhibitors Acequinocyl, fluacrypyrim Microbial disruptors of the insect ut membrane Bacillus thuriniensis strains Fat synthesis inhibitors tetronic acids, for example spirodiclofen, spiromesifen tetramic acids, for example spirotetramat (CAS Re. No.: 20333-25-) and 3-(2,5-dimethylphenyl)-- methoxy-2-oxo-l-azaspiro[4.5]dec-3-en-4-yl ethyl carbonate (also known as: carbonic acid, 3-(2,5-dimethylphenyl)--methoxy-2-oxo-l-azaspiro[4.5]dec-3-en-4-yl ethyl ester, CAS Re. No.: 3260-0-) carboxamides, -36- for example flonicamid octopamineric aonists, for example amitraz Inhibitors of manesium-stimulated ATPase, proparite benzoic acid dicarboxamides, for example flubendiamides nereistoxin analos for example thiocyclam hydroen oxalate, thiosultap-sodium Bioloicals, hormones or pheromones azadirachtin, Bacillus spec., Beauveria spec., codlemone, Metarrhizium spec., Paecilomyces spec., thuriniensin, Verticillium spec. Active compounds with unknown or unspecific mechanisms of action 23. Fumiants, for example aluminum phosphide, methyl bromide, sulfuryl fluoride 23.2 Antifeedants, for example cryolite, flonicamid, pymetrozine 23.3 Mite rowth inhibitors, for example clofentezine, etoxazole, hexythiazox 23.4 Amidoflumet, benclothiaz, benzoximate, bifenazate, bromopropylate, buprofezin, chinomethionat, chlordimeform, chlorobenzilate, chloropicrin, clothiazoben, cycloprene, cyflumetofen, dicyclanil, fenoxacrim, fentrifanil, flubenzimine, flufenerim, flutenzin, ossyplure, hydramethylnone, aponilure, metoxadiazone, petroleum, piperonyl butoxide, potassium oleate, pyridalyl, sulfluramid, tetradifon, tetrasul, triarathene, verbutin A mixture with other known active compounds, such as herbicides, fertilizers, rowth reulators, safeners, semiochemicals, or else with aents which improve plant properties is also possible. When used as insecticides in their commercially available formulations and in the use forms prepared from these formulations, the active compounds/active compound combinations accordin to the invention can furthermore be present in the form of a mixture with synerists. Synerists are compounds by which the activity of the active compounds is increased without it bein necessary for the synerist added to be active itself. When used as insecticides in their commercially available formulations and in the use forms prepared from these formulations, the active compounds/active compound combinations accordin to the invention can furthermore be present in the form of mixtures with inhibitors which reduce the deradation of the active compound after application in the habitat of the plant, on the surface of parts of plants or in plant tissues. The active compound content of the use forms prepared from the commercially available formulations can vary within wide ranes. The active compound concentration of the use forms can be from 0.0000000 up to 95% by weiht of active compound and is preferably between 0.0000 and % by weiht. Application is in a customary manner adapted to suit the use forms. As already mentioned above, it is possible to treat all plants and their parts in accordance with the invention. In a preferred embodiment, wild plant species or plant varieties and plant cultivars which have been obtained by traditional bioloical breedin methods, such as hybridization or protoplast fusion, and the parts of these varieties and cultivars are treated. In a further preferred embodiment, transenic plants and plant cultivars which have been obtained by recombinant methods, if appropriate in combination with conventional methods (enetically modified oranisms), and their parts are treated. The term "parts" or "parts of plants" or "plant parts" has been explained above. Plants which are treated particularly preferably in accordance with the invention are those of the plant cultivars which are in each case commercially available or in use. Plant cultivars are understood as meanin plants with new traits which have been bred either by conventional breedin, by mutaenesis or by recombinant DNA techniques. They may take the form of cultivars, biotypes and enotypes. Dependin on the plant species or plant cultivars, their location and rowth conditions (soils, climate, veetation period, nutrition), the treatment accordin to the invention may also result in superadditive ("syneristic") effects. Thus, for example, reduced application rates and/or a widened activity spectrum and/or an increase in the activity of the substances and compositions which can be used in accordance with the invention, better plant rowth, increased tolerance to hih or low temperatures, increased tolerance to drouht or to salinity in the water or soil, increased flowerin performance, facilitated harvestin, accelerated maturation, hiher yields, hiher quality and/or better nutritional value of the harvested products, better storae characteristics and/or processability of the harvested products are possible which exceed the effects which were actually to be expected. The preferred transenic plants or plant cultivars (those obtained by recombinant methods) to be treated in accordance with the invention include all those plants which, owin to the process of recombinant modification, were iven enetic material which confers particular, advantaeous, valuable traits to these plants. Examples of such properties are better plant rowth, increased tolerance to hih or low temperatures, increased tolerance to drouht or to salinity in the water or soil, increased flowerin performance, facilitated harvestin, accelerated maturation, hiher harvest yields, hiher quality and/or hiher nutritional value of the harvested products, better storae characteristics and/or better processability of the harvested products. Further examples of such traits, examples which must be mentioned especially, are .better defense of the plants aainst animal and microbial pests, such as aainst insects, mites, phytopathoenic funi, bacteria and/or viruses and an increased tolerance of the plants to certain herbicidal active compounds. Examples of transenic plants which may be mentioned are the important crop plants, such as cereals (wheat, rice), maize, soybeans, potato, suar beet, tomatoes, peas and other veetable varieties, cotton, tobacco, oilseed rape and fruit plants (with the fruits apples, pears, citrus fruits and rapes), with particular emphasis on maize, soybeans, potatoes, cotton, tobacco, and oilseed rape. Traits which are especially emphasized are the increased defense of the plants aainst insects, arachnids, nematodes and slus and snails, owin to toxins bein formed in the plants, in particular toxins which are enerated in the plants by the enetic material of Bacillus thuriniensis (for example by the enes CrylA(a), CrylA(b), CrylA(c), CryllA, CrylllA, CryIIIB2, Cry9c Cry2Ab, Cry3Bb and Cry IF and their combinations (hereinbelow "Bt plants"). Other traits which are particularly emphasized are the increased defense of plants aainst funi, bacteria and viruses by the systemic acquired resistance (SAR), systemins, phytoalexins, elicitors and resistance enes and correspondinly expressed proteins and toxins. Other traits which are especially emphasized are the increased tolerance of the plants to certain herbicidal active compounds, for example imidazolinones, sulfonylureas, lyphosate or phosphinotricin (for example "PAT" ene). The enes which confer the desired traits in each case may also be present in the transenic plants in combination with one another. Examples of "Bt plants" which may be mentioned are maize cultivars, cotton cultivars, soybean cultivars and potato cultivars which are commercially available under the trade names YIELD ARD® (for example maize, cotton, soybeans), KnockOut® (for example maize), StarLink® (for example maize), Bollard® (cotton), Nucotn® (cotton) and NewLeaf® (potato). Examples of herbicide-tolerant plants which may be mentioned are maize cultivars, cotton cultivars and soybean cultivars which are commercially available under the trade names Roundup Ready® (tolerance to lyphosate, for example maize, cotton, soybeans), Liberty Link® (tolerance to phosphinotricin, for example oilseed rape), IMI® (tolerance to imidazolinones) and STS® (tolerance to sulfonylureas, for example maize). Herbicideresistant plants (plants bred in a conventional manner for herbicide tolerance) which may be mentioned also include the varieties commercially available under the name Clearfield® (for example maize). Naturally, these statements also apply to plant cultivars havin these enetic traits or enetic traits still to be developed, which plant cultivars will be developed and/or marketed in the future. The plants listed can be treated particularly advantaeously accordin to the invention with the compounds of the eneral formula or the active compound mixtures accordin to the invention. The preferred ranes stated above for the active compounds and mixtures also apply to the treatment of these plants. Particular emphasis may be iven to the treatment of plants with the compounds or mixtures specifically mentioned in the present text. The active compounds/active compound combinations accordin to the invention are not only active aainst plant, hyiene and stored-product pests, but also, in the veterinary medicine sector, aainst animal parasites (ectoparasites and endoparasites), such as ixodid ticks, arasid ticks, scab mites, trombiculid mites, flies (stinin and suckin), parasitic fly larvae, lice, hair lice, bird lice and fleas. These parasites include: From the order of the Anoplurida, for example, Haematopinus spp., Linonathus spp., Pediculus spp., Phtirus spp., Solenopotes spp. From the order of the Mallophaida and the sub-orders Amblycerina and Ischnocerina, for example, Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes spp., Felicola spp. From the order of the Diptera and the sub-orders Nematocerina and Brachycerina, for example, Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., hrysops spp., Hybomitra spp., Atylotus spp., Tabanus spp., Haematopota spp., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., lossina spp., Calliphora spp., Lucilia spp., Chrysomyia spp., Wohlfahrtia spp., Sarcophaa spp., Oestrus spp., Hypoderma spp., asterophilus spp., Hippobosca spp., Lipoptena spp. and Melophaus spp. From the order of the Siphonapterida, for example, Pulex spp., Ctenocephalides spp., Xenopyslla spp. and Ceratophyllus spp. From the order of the Heteropterida, for example, Cimex spp., Triatoma spp., Rhodnius spp. and Panstronylus spp. From the order of the Blattarida, for example, Blatta orientalis, Periplaneta americana, Blattela ermanica and Supella spp. From the sub-class of the Acari (Acarina) and the orders of the Meta- and Mesostimata, for example, Aras spp., Ornithodorus spp., Otobius spp., Ixodes spp., Amblyomma spp., Boophilus spp., Dermacentor spp., Haemophysalis spp., Hyalomma spp., Rhipicephalus spp., Dermanyssus spp., Raillietia spp., Pneumonyssus spp., Sternostoma spp. and Varroa spp. From the order of the Actinedida (Prostimata) and Acaridida (Astimata), for example, Acarapis spp., Cheyletiella spp., Ornithocheyletia spp., Myobia spp., Psorerates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophaus spp., Calolyphus spp., Hypodectes spp., Pterolichus spp., Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp. and Laminosioptes spp. The active compounds/active compound combinations of the formula (I) accordin to the invention are also suitable for controllin arthropods which attack aricultural livestock, such as, for example, cattle, sheep, oats, horses, pis, donkeys, camels, buffaloes, rabbits, chickens, turkeys, ducks, eese, honeybees, other domestic animals, such as, for example, dos, cats, cae birds, aquarium fish, and so-called experimental animals, such as, for example, hamsters, uinea-pis, rats and mice. By combatin these arthropods, it is intended to reduce deaths and decreased performances (in meat, milk, wool, hides, es, honey and the like), so that more economical and simpler animal keepin is made possible by usin the active compounds accordin to the invention. In the veterinary sector, the active compounds/active compound combinations accordin to the invention are used in a known manner by enteral administration, for example in the form of tablets, capsules, drinks, drenches, ranules, pastes, boli, the feed-throuh method, suppositories, by parenteral administration, such as, for example, by means of inections (intramuscular, subcutaneous, intravenous, intraperitoneal and the like), implants, by nasal application, by dermal administration, for example in the form of dippin or bathin, sprayin, pourin-on and spottinon, washin, dustin, and with the aid of shaped articles which comprise active compound, such as collars, ear tas, tail marks, limb bands, halters, markin devices and the like. When administered to livestock, poultry, domestic animals and the like, the active compounds of the formula (I) can be used as formulations (for example powders, emulsions, flowables) which comprise the active compounds in an amount of to 0% by weiht, either directly or after dilution by a factor of 00 to 0 000, or they may be used in the form of a chemical bath. Furthermore, it has been found that the compounds/active compound combinations accordin to the invention have a potent insecticidal action aainst insects which destroy industrial materials. The followin insects may be mentioned by way of example and as bein preferred, but without any limitation: Beetles, such as Hylotrupes baulus, Chlorophorus pilosis, Anobium punctatum, Xestobium rufovillosum, Ptilinus pecticornis, Dendrobium pertinex, Ernobius mollis, Priobium carpini, Lyctus brunneus, Lyctus africanus, Lyctus planicollis, Lyctus linearis, Lyctus pubescens, Trooxylon aequale, Minthes ruicollis, Xyleborus spec. Tryptodendron spec. Apate monachus, Bostrychus capucins, Heterobostrychus brunneus, Sinoxylon spec. Dinoderus minutus; Dermapterans, such as Sirex uvencus, Urocerus ias, Urocerus ias tainus, Urocerus auur; Termites, such as Kalotermes flavicollis, Cryptotermes brevis, Heterotermes indicola, Reticulitermes flavipes, Reticulitermes santonensis, Reticulitermes lucifuus, Mastotermes darwiniensis, Zootermopsis nevadensis, optotermes. formosanus; Bristletails, such as Lepisma saccharina. Industrial materials are to be understood as meanin, in the present context, non-live materials, such as, preferably, synthetic materials, lues, sizes, paper and board, leather, wood and timber products, and paint. The materials to be very particularly preferably protected aainst attack by insects are wood and timber products. Wood and timber products which can be protected by the composition accordin to the invention or mixtures comprisin such a composition are to be understood as meanin, for example: construction timber, wooden beams, railway sleepers, bride components, etties, wooden vehicles, boxes, pallets, containers, telephone poles, wood claddin, windows and doors made of wood, plywood, particle board, oiner's articles, or wood products which, quite enerally, are used in the construction of houses or in oinery. -42- The active compounds can be used as such, in the form of concentrates or enerally customary formulations, such as powders, ranules, solutions, suspensions, emulsions or pastes. The formulations mentioned can be prepared in a manner known per se, for example by mixin the active compounds with at least one solvent or diluent, emulsifier, dispersant and/or binder or fixative, water repellent, if appropriate desiccants and UV stabilizers and, if appropriate, colorants and piments and other processin auxiliaries. The insecticidal compositions or concentrates used for the protection of wood and wooden materials comprise the active compound accordin to the invention in a concentration of 0.000 to 95% by weiht, in particular 0.00 to 60% by weiht. The amount of the compositions or concentrates employed depends on the species and the occurrence of the insects and on the medium. The optimum rate of application can be determined upon use in each case by a test series. However, in eneral, it suffices to employ 0.000 to 20% by weiht, preferably 0.00 to 0% by weiht, of the active compound, based on the material to be protected. The solvent and/or diluent used is an oranochemical solvent or solvent mixture and/or an oily or oil-type oranochemical solvent or solvent mixture of low volatility and/or a polar oranochemical solvent or solvent mixture and/or water and, if appropriate, an emulsifier and/or wettin aent. Oranochemical solvents which are preferably employed are oily or oil-type solvents havin an evaporation number of above 35 and a flash point of above 30°C, preferably above 45°C. Substances which are used as such oily and oil-type solvents which have low volatility and are insoluble in water are suitable mineral oils or their aromatic fractions, or mineral-oil-containin solvent mixtures, preferably white spirit, petroleum and/or alkylbenzene. Substances which are advantaeously used are mineral oils with a boilin rane of 70 to 220°C, white spirit with a boilin rane of 70 to 220°C, spindle oil with a boilin rane of 250 to 350°C, petroleum or aromatics of boilin rane 60 to 20°C, essence of turpentine and the like. In a preferred embodiment, liquid aliphatic hydrocarbons with a boilin rane of 0 to 20°C or hih-boilin mixtures of aromatic and aliphatic hydrocarbons with a boilin rane of 0 to 220°C and/or spindle oil and/or monochloronaphthalene, preferably a-monochloronaphthalene, are used. The oranic oily or oil-type solvents of low volatility havin an evaporation number of above and a flash point of above 30°C, preferably above 45°C, can be partially replaced by oranochemical solvents of hih or medium volatility, with the proviso that the solvent mixture also has an evaporation number of above 35 and a flash point of above 30°C, preferably above 45°C, and that the insecticide/funicide mixture is soluble or emulsifiable in this solvent mixture. In a preferred embodiment, part of the oranochemical solvent or solvent mixture or an aliphatic polar oranochemical solvent or solvent mixture is replaced. Substances which are preferably used are aliphatic oranochemical solvents havin hydroxyl and/or ester and/or ether roups, such as, for example, lycol ethers, esters and the like. The oranochemical binders used within the scope of the present invention are the synthetic resins and/or bindin dryin oils which are known per se and can be diluted with water and/or are soluble or dispersible or emulsifiable in the oranochemical solvents employed, in particular binders composed of, or comprisin, an acrylate resin, a vinyl resin, for example polyvinyl acetate, polyester resin, polycondensation or polyaddition resin, polyurethane resin, alkyd resin or modified alkyd resin, phenol resin, hydrocarbon resin, such as indene/cumarone resin, silicone resin, dryin veetable and/or dryin oils and/or physically dryin binders based on a natural and/or synthetic resin. The synthetic resin used as the binder can be employed in the form of an emulsion, dispersion or solution. Up to 0% by weiht of bitumen or bituminous substances can also be used as binders. In addition, colorants, piments, water repellents, odor-maskin substances and inhibitors or anticorrosives known per se and the like can also be employed. The composition or the concentrate preferably comprises, in accordance with the invention, at least one alkyd resin or modified alkyd resin and/or a dryin veetable oil as the oranochemical binder. Preferably used accordin to the invention are alkyd resins with an oil content of over 45% by weiht, preferably 50 to 6% by weiht. All or some of the abovementioned binder can be replaced by a fixative (mixture) or a plasticizer (mixture). These additives are intended to prevent volatilization of the active compounds and crystallization or precipitation. They preferably replace 0.0 to 30% of the binder (based on 00% of binder employed). The plasticizers are from the chemical classes of the phthalic esters, such as dibutyl phthalate, dioctyl phthalate or benzyl butyl phthalate, the phosphoric esters, such as tributyl phosphate, the adipic esters, such as di(2-ethylhexyl) adipate, the stearates, such as butyl stearate or amyl stearate, the oleates, such as butyl oleate, the lycerol ethers or relatively hih molecular weiht lycol ethers, lycerol esters and p-toluenesulfonic esters. - 44- Fixatives are chemically based on polyvinyl alkyl ethers, such as, for example, polyvinyl methyl ether, or ketones, such as benzophenone or ethylenebenzophenone. Particularly suitable as a solvent or diluent is also water, if appropriate as a mixture with one or more of the abovementioned oranochemical solvents or diluents, emulsifiers and dispersants. Particularly effective protection of wood is achieved by lare-scale industrial imprenation processes, for example vacuum, double-vacuum or pressure processes. If appropriate, the ready-to-use compositions can additionally comprise other insecticides and, if appropriate, additionally one or more funicides. Suitable additional components which may be admixed are, preferably, the insecticides and funicides mentioned in WO 94/29 26. The compounds mentioned in that document are expressly part of the present application. Very particularly preferred components which may be admixed are insecticides, such as chlorpyriphos, phoxim, silafluofm, alphamethrin, cyfluthrin, cypermethrin, deltamethrin, permethrin, imidacloprid, NI-25, flufenoxuron, hexaflumuron, transfluthrin, thiacloprid, methoxyphenoxid, triflumuron, chlothianidin, spinosad, tefluthrin, and funicides, such as epoxyconazole, hexaconazole, azaconazole, propiconazole, tebuconazole, cyproconazole, metconazole, imazalil, dichlorfluanid, tolylfluanid, 3-iodo-2-propynyl butylcarbamate, N-octyl-isothiazolin-3-one and 4,5-dichloro-N-octylisothiazolin-3-one. The compounds accordin to the invention can at the same time be employed for protectin obects which come into contact with saltwater or brackish water, in particular hulls, screens, nets, buildins, moorins and sinalin systems, aainst foulin. Foulin by sessile Oliochaeta, such as Serpulidae, and by shells and species from the Ledamorpha roup (oose barnacles), such as various Lepas and Scalpellum species, or by species from the Balanomorpha roup (acorn barnacles), such as Balanus or Pollicipes species, increases the frictional dra of ships and, as a consequence, leads to a marked increase in operation costs owin to hiher enery consumption and additionally frequent residence in the dry dock. Apart from foulin by alae, for example Ectocarpus sp. and Ceramium sp., foulin by sessile Entomostraka roups, which come under the eneric term Cirripedia (cirriped crustaceans), is of particular importance. Surprisinly, it has now been found that the compounds accordin to the invention, alone or in combination with other active compounds, have an outstandin antifoulin action. Usin the compounds accordin to the invention, alone or in combination with other active compounds, allows the use of heavy metals such as, for example, in bis(trialkyltin) sulfides, tri-rcbutyltin laurate, tri-butyltin chloride, copper(I) oxide, triethyltin chloride, tri-«-butyl-(2-phenyl- 4-chlorophenoxy)tin, tributyltin oxide.; molybdenum disulfide, antimony oxide, polymeric butyl titanate, phenyl(bispyridine)bismuth chloride, tri-«-butyltin fluoride, mananese ethylenebisthiocarbamate, zinc dimethyldithiocarbamate, zinc ethylenebisthiocarbamate, zinc salts and copper salts of 2-pyridinethiol -oxide, bisdimethyldithiocarbamoylzinc ethylenebisthiocarbamate, zinc oxide, copper(I) ethylenebisdithiocarbamate, copper thiocyanate, copper naphthenate and tributyltin halides to be dispensed with, or the concentration of these compounds to be substantially reduced. If appropriate, the ready-to-use antifoulin paints can additionally comprise other active compounds, preferably alicides, funicides, herbicides, molluscicides, or other antifoulin active compounds. Preferably suitable components in combination with the antifoulin compositions accordin to the invention are: alicides such as 2-/e-butylamino-4-cyclopropylamino-6-methylthio-l,3,5-triazine, dichlorophen, diuron, endothal, fentin acetate, isoproturon, methabenzthiazuron, oxyfluorfen, quinoclamine and terbutryn; funicides such as benzo[£]thiophenecarboxylic acid cyclohexylamide S,S-dioxide, dichlofluanid, fluorfolpet, 3-iodo- 2-propynyl butylcarbamate, tolylfluanid and azoles such as azaconazole, cyproconazole, epoxyconazole, hexaconazole, metconazole, propiconazole and tebuconazole; molluscicides such as fentin acetate, metaldehyde, methiocarb, niclosamid, thiodicarb and trimethacarb, Fe chelates; or conventional antifoulin active compounds such as 4,5-dichloro-2-octyl-4-isothiazolin-3-one, diiodomethylparatryl sulfone, 2-(N,N-dimethylthiocarbamoylthio)- 5-nitrothiazyl, potassium, copper, sodium and zinc salts of 2-pyridinethiol -oxide, pyridine-triphenylborane, tetrabutyldistannoxane, 2,3,5,6-tetrachloro-4-(methylsulfonyl)- pyridine, 2,4,5,6-tetrachloroisophthalonitrile, tetramethylthiuram disulfide and 2,4,6- trichlorophenylmaleimide. The antifoulin compositions used comprise the active compound accordin to the invention of the compounds accordin to the invention in a concentration of 0.00 to 50% by weiht, in particular 0.0 to 20% by weiht. Moreover, the antifoulin compositions accordin to the invention comprise the customary components such as, for example, those described in Unerer, Chem. Ind, 95, 37, 730-732 and Williams, Antifoulin Marine Coatins, Noyes, Park Ride, 973. Besides the alicidal, funicidal, moliuscicidal active compounds and insecticidal active compounds accordin to the invention, antifoulin paints comprise, in particular, binders. Examples of reconized binders are polyvinyl chloride in a solvent system, chlorinated rubber in a solvent system, acrylic resins in a solvent system, in particular in an aqueous system, vinyl chloride/vinyl acetate copolymer systems in the form of aqueous dispersions or in the form of oranic solvent systems, butadiene/styrene/acrylonitrile rubbers, dryin oils such as linseed oil, resin esters or modified hardened resins in combination with tar or bitumens, asphalt and epoxy compounds, small amounts of chlorine rubber, chlorinated polypropylene and vinyl resins. If appropriate, paints also comprise inoranic piments, oranic piments or colorants which are preferably insoluble in saltwater. Paints may furthermore comprise materials such as rosin to allow controlled release of the active compounds. Furthermore, the paints may comprise plasticizers, modifiers which affect the rheoloical properties and other conventional constituents. The compounds accordin to the invention or the abovementioned mixtures may also be incorporated into self-polishin antifoulin systems. The active compounds are also suitable for controllin animal pests, in particular insects, arachnids and mites, which are found in enclosed spaces such as, for example, dwellins, factory halls, offices, vehicle cabins and the like. They can be employed in domestic insecticide products for controllin these pests alone or in combination with other active compounds and auxiliaries. They are active aainst sensitive and resistant species and aainst all development staes. These pests include: From the order of the Scorpionidea, for example, Buthus occitanus. From the order of the Acarina, for example, Aras persicus, Aras reflexus, Bryobia ssp., Dermanyssus allinae, lyciphaus domesticus, Ornithodorus moubat, Rhipicephalus sanuineus, Trombicula alfredduesi, Neutrombicula autumnalis, Dermatophaoides pteronissimus, Dermatophaoides forinae. From the order of the Araneae, for example, Aviculariidae, Araneidae. From the order of the Opiliones, for example, Pseudoscorpiones chelifer, Pseudoscorpiones cheiridium, Opiliones phalanium. From the order of the Isopoda, for example, Oniscus asellus, Porcellio scaber. From the order of the Diplopoda, for example, Blaniulus uttulatus, Polydesmus spp. From the order of the Chilopoda, for example, eophilus spp. From the order of the Zyentoma, for example, Ctenolepisma spp., Lepisma saccharina, Lepismodes inquilinus. From the order of the Blattaria, for example, Blatta orientalies, Blattella ermanica, Blattella asahinai, Leucophaea maderae, Panchlora spp., Parcoblatta spp., Periplaneta australasiae, Periplaneta americana, Periplaneta brimnea, Periplaneta fuliinosa, Supella lonipalpa. From the order of the Saltatoria, for example, Acheta domesticus. From the order of the Dermaptera, for example, Forficula auricularia. From the order of the Isoptera, for example, Kalotermes spp., Reticulitermes spp. From the order of the Psocoptera, for example, Lepinatus spp., Liposcelis spp. From the order of the Coleptera, for example, Anthrenus spp., Attaenus spp., Dermestes spp., Latheticus oryzae, Necrobia spp., Ptinus spp., Rhizopertha dominica, Sitophilus ranarius, Sitophilus oryzae, Sitophilus zeamais, Steobium paniceum. From the order of the Diptera, for example, Aedes aeypti, Aedes albopictus, Aedes taeniorhynchus, Anopheles spp., Calliphora erythrocephala, Chrysozona pluvialis, Culex quinquefasciatus, Culex pipiens, Culex tarsalis, Drosophila spp., Fannia canicularis, Musca domestica, Phlebotomus spp., Sarcophaa carnaria, Simulium spp., Stomoxys calcitrans, Tipula paludosa. From the order of the Lepidoptera, for example, Achroia risella, alleria mellonella, Plodia interpunctella, Tinea cloacella, Tinea pellionella, Tineola bisselliella. From the order of the Siphonaptera, for example, Ctenocephalides canis, Ctenocephalides felis, Pulex irritans, Tuna penetrans, Xenopsylla cheopis. From the order of the Hymenoptera, for example, Camponotus herculeanus, Lasius fuliinosus, Lasius nier, Lasius umbratus, Monomorium pharaonis, Paravespula spp., Tetramorium caespitum. From the order of the Anoplura, for example, Pediculus humanus capitis, Pediculus humanus corporis, Phthirus pubis. From the order of the Heteroptera, for example, Cimex hemipterus, Cimex lectularius, Rhodinus prolixus, Triatoma infestans. They are used in the household insecticides sector alone or in combination with other suitable active compounds such as phosphoric esters, carbamates, pyrethroids, neonicotinoids, rowth reulators or active compounds from other known classes of insecticides. They are used in aerosols, pressure-free spray products, for example pump and atomizer sprays, automatic foin systems, foers, foams, els, evaporator products with evaporator tablets made of cellulose or polymer, liquid evaporators, el and membrane evaporators, propeller-driven evaporators, enery-free, or passive, evaporation systems, moth papers, moth bas and moth els, as ranules or dusts, in baits for spreadin or in bait stations. The active compounds/active compound combinations accordin to the invention can also be used as defoliants, desiccants, haulm killers and, in particular, as weed killers. Weeds in the broadest sense are understood as meanin all plants which row at locations where they are undesired. Whether the substances accordin to the invention act as nonselective or selective herbicides depends essentially on the application rate. The active compounds/active compound combinations accordin to the invention can be used, for example, in the followin plants: Dicotyledonous weeds of the enera: Abutilon, Amaranthus, Ambrosia, Anoda, Anthemis, Aphanes, Atriplex, Bellis, Bidens, Capsella, Carduus, Cassia, Centaurea, Chenopodium, Cirsium, Convolvulus, Datura, Desmodium, Emex, Erysimum, Euphorbia, aleopsis, alinsoa, alium, Hibiscus, Ipomoea, Kochia, Lamium, Lepidium, Lindernia, Matricaria, Mentha, Mercurialis, Mulluo, Myosotis, Papaver, Pharbitis, Plantao, Polyonum, Portulaca, Ranunculus, Raphanus, Rorippa, Rotala, Rumex, Salsola, Senecio, Sesbania, Sida, Sinapis, Solanum, Sonchus, Sphenoclea, Stellaria, Taraxacum, Thlaspi, Trifolium, Urtica, Veronica, Viola, Xanthium. icotyledonous crops of the enera: Arachis, Beta, Brassica, Cucumis, Cucurbita, Helianthus, Daucus, lycine, ossypium, Ipomoea, Lactuca, Linum, Lycopersicon, Nicotiana, Phaseolus, Pisum, Solanum, Vicia. Monocotyledonous weeds of the enera: Aeilops, Aropyron, Arostis, Alopecurus, Apera, Avena, Brachiaria, Bromus, Cenchrus, Commelina, Cynodon, Cyperus, Dactyloctenium, Diitaria, Echinochloa, Eleocharis, Eleusine, Erarostis, Eriochloa, Festuca, Fimbristylis, Heteranthera, Imperata, Ischaemum, Leptochloa, Lolium, Monochoria, Panicum, Paspalum, Phalaris, Phleum, Poa, Rottboellia, Saittaria, Scirpus, Setaria, Sorhum. Monocotyledonous crops of the enera: Allium, Ananas, Asparaus, Avena, Hordeum, Oryza, Panicum, Saccharum, Secale, Sorhum, Triticale, Triticum, Zea. However, the use of the active compounds/active compound combinations accordin to the invention is in no way restricted to these enera, but extends in the same manner to other plants. Dependin on the concentration, the active compounds/active compound combinations accordin to the invention are suitable for the nonselective weed control on, for example, industrial terrains and railway tracks and on paths and locations with and without trees. Likewise the active compounds accordin to the invention can be employed for controllin weeds in perennial crops, for example forests, ornamental tree plantins, orchards, vineyards, citrus roves, nut orchards, banana plantations, coffee plantations, tea plantations, rubber plantations, oil palm plantations, cocoa plantations, soft fruit plantations and hop fields, on lawns, turf and pastureland, and for the selective control of weeds in annual crops. The compounds of the formula (I)/active compound combinations accordin to the invention have stron herbicidal activity and a broad activity spectrum when used on the soil and on aerial plant parts. To a certain extent, they are also suitable for the selective control of monocotyledonous and dicotyledonous weeds in monocotyledonous and dicotyledonous crops, both pre- and postemerence. At certain concentrations or application rates, the active compounds/active compound combinations accordin to the invention can also be employed for controllin animal pests and funal or bacterial plant diseases. If appropriate, they can also be used as intermediates or precursors for the synthesis of other active compounds. The active compounds/active compound combinations can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, dustin aents, pastes, soluble powders, ranules, suspoemulsion concentrates, natural and synthetic materials imprenated with active compound, and very fine capsules in polymeric substances. These formulations are produced in a known manner, for example by mixin the active compounds with extenders, that is liquid solvents and/or solid carriers, optionally with the use of surfactants, that is emulsifiers and/or dispersants and/or foam-formers. If the extender used is water, it is also possible to use, for example, oranic solvents as auxiliary solvents. Suitable liquid solvents are essentially: aromatics, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and veetable oils, alcohols, such as butanol or lycol, and also their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, stronly polar solvents, such as dimethylformamide and dimethyl sulfoxide, and also water. Suitable solid carriers are: for example ammonium salts and round natural minerals, such as kaolins, clays, talc, chalk, quartz, attapulite, montmorillonite or diatomaceous earth, and round synthetic minerals, such as finely divided silica, alumina and silicates, suitable solid carriers for ranules are: for example crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, and also synthetic ranules of inoranic and oranic meals, and ranules of oranic material such as sawdust, coconut shells, maize cobs and tobacco stalks; suitable emulsifiers and/or foam-formers are: for example nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polylycol ethers, alkylsulfonates, alkyl sulfates, arylsulfonates and protein hydrolyzates; suitable dispersants are: for example linosulfite waste liquors and methylcellulose. Tackifiers such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, ranules or latices, such as um arabic, polyvinyl alcohol and polyvinyl acetate, and also natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids, can be used in the formulations. Other possible additives are mineral and veetable oils. It is possible to use colorants such as inoranic piments, for example iron oxide, titanium oxide and Prussian blue, and oranic colorants, such as alizarin colorants, azo colorants and metal phthalocyanine colorants, and trace nutrients such as salts of iron, mananese, boron, copper, cobalt, molybdenum and zinc. The formulations enerally comprise between 0. and 95 per cent by weiht of active compound, preferably between 0.5 and 90%. The active compounds/active compound combinations accordin to the invention, as such or in their formulations, can also be used for weed control purposes as a mixture with known herbicides and/or with substances which improve crop plant tolerance ("safeners"), ready mixes or tank mixes bein possible. Mixtures with herbicide products which contain one or more known herbicides and a safener are hence also possible. Herbicides which are suitable for the mixtures are known herbicides, for example acetochlor, acifluorfen (-sodium), aclonifen, alachlor, alloxydim (-sodium), ametryne, amicarbazone, amidochlor, amidosulfuron, aminopyralid, anilofos, asulam, atrazine, azafenidin, azimsulfuron, beflubutamid, benazolin (-ethyl), benfuresate, bensulfuron (-methyl), bentazone, bencarbazone, benzfendizone, benzobicyclon, benzofenap, benzoylprop (-ethyl), bialaphos, bifenox, bispyribac (-sodium), bromobutide, bromofenoxim, bromoxynil, butachlor, butafenacil (-allyl), butroxydim, butylate, cafenstrole, caloxydim, carbetamide, carfentrazone (-ethyl), chlomethoxyfen, chloramben, chloridazon, chlorimuron (-ethyl), chlornitrofen, chlorsulfuron, chlortoluron, cinidon (-ethyl), cinmethylin, cinosulfuron, clefoxydim, clethodim, clodinafop (-proparyl), clomazone, clomeprop, clopyralid, clopyrasulfuron (-methyl), cloransulam (-methyl), cumyluron, cyanazine, cybutryne, cycloate, cyclosulfamuron, cycloxydim, cyhalofop (-butyl), 2,4- D, 2,4-DB, desmedipham, diallate, dicamba, dichlorprop (-P), diclofop (-methyl), diclosulam, diethatyl (-ethyl), difenzoquat, diflufenican, diflufenzopyr, dimefuron, dimepiperate, dimethachlor, dimethametryn, dimethenamid, dimexyflam, dinitramine, diphenamid, diquat, dithiopyr, diuron, dymron, epropodan, EPTC, esprocarb, ethalfluralin, ethametsulfuron (-methyl), ethofumesate, ethoxyfen, ethoxysulfuron, etobenzanid, fenoxaprop (-P-ethyl), fentrazamide, flamprop (-isopropyl, -isopropyl-L, -methyl), flazasulfuron, florasulam, fluazifop (-P-butyl), fluazolate, flucarbazone (-sodium), flufenacet, flumetsulam, flumiclorac (-pentyl), flumioxazin, flumipropyn, flumetsulam, fluometuron, fluorochloridone, fluorolycofen (-ethyl), flupoxam, flupropacil, flurpyrsulfuron (-methyl, -sodium), flurenol (-butyl), fluridone, fluroxypyr (-butoxypropyl, -meptyl), flurprimidol, flurtamone, fluthiacet (-methyl), fluthiamide, fomesafen, foramsulfuron, lufosinate (-ammonium), lyphosate (-isopropylammonium), halosafen, haloxyfop (-ethoxyethyl, -P-methyl), hexazinone, HOK-20, imazamethabenz (-methyl), imazamethapyr, imazamox, imazapic, imazapyr, imazaquin, imazethapyr, imazosulfuron, iodosulfuron (-methyl, -sodium), ioxynil, isopropalin, isoproturon, isouron, isoxaben, isoxachlortole, isoxaflutole, isoxapyrifop, KIH 45, lactofen, lenacil, linuron, MCPA, mecoprop, mefenacet, mesosulfuron, mesotrione, metamifop, metamitron, metazachlor, methabenzthiazuron, metobenzuron, metobromuron, (alpha-) metolachlor, metosulam, metoxuron, metribuzin, metsulfuron (-methyl), molinate, monolinuron, naproanilide, napropamide, neburon, nicosulfuron, norflurazon, orbencarb, orthosulfamuron, oryzalin, oxadiaryl, oxadiazon, oxasulfuron, oxaziclomefone, oxyfluorfen, paraquat, pelaronic acid, pendimethalin, pendralin, penoxsulam, pentoxazone, phenmedipham, picolinafen, pinoxaden, piperophos, pretilachlor, primisulfuron (-methyl), profluazol, prometryn, propachlor, propanil, propaquizafop, propisochlor, propoxycarbazone (-sodium), propyzamide, prosulfocarb, prosulfuron, pyraflufen (-ethyl), pyrasulfotole, pyrazoyl, pyrazolate, pyrazosulfuron (-ethyl), pyrazoxyfen, pyribenzoxim, pyributicarb, pyridate, pyridatol, pyriftalide, pyriminobac (-methyl), pyrimisulfan, pyrithiobac (-sodium), quinchlorac, quinmerac, quinoclamine, quizalofop (-P-ethyl, -P-tefuryl), rimsulfuron, sethoxydim, simazine, simetryn, sulcotrione, sulfentrazone, sulfometuron (-methyl), sulfosate, sulfosulfuron, tebutam, tebuthiuron, tembotrione, tepraloxydim, terbuthylazine, terbutryn, thenylchlor, thiafluamide, thiazopyr, thidiazimin, thifensulfuron (-methyl), thiobencarb, tiocarbazil, topramezone, tralkoxydim, triallate, triasulfuron, tribenuron (-methyl), triclopyr, tridiphane, trifluralin, trifloxysulfuron, triflusulfuron (-methyl), tritosulfuron and A mixture with other known active compounds, such as funicides, insectides, acaricides, nematicides, bird repellents, plant nutrients and soil conditioners, is also possible. The active compounds/active compound combinations can be applied as such, in the form of their formulations or the use forms prepared therefrom by further dilution, such as ready-to-use solutions, suspensions, emulsions, powders, pastes and ranules. They are applied in the customary manner, for example by pourin, sprayin, atomizin, spreadin. The active compounds/active compound combinations accordin to the invention can be applied both before and after plant emerence. They can also be incorporated into the soil prior to. plantin. The application rate of active compound can vary within a substantial rane. Essentially, it depends on the nature of the desired effect. In eneral, the application rates are between and 0 k of active compound per hectare of soil area, preferably between 5 and 5 k per ha. The advantaeous effect of the compatibility with crop plants of the active compound combinations accordin to the invention is particularly pronounced at certain concentration ratios. However, the weiht ratios of the active compounds in the active compound combinations can be varied within relatively wide ranes. In eneral, from 0.00 to 000 parts by weiht, preferably from 0.0 to 00 parts by weiht, particularly preferably 0.05 to 20 parts by weiht, of one of the compounds which improves crop plant compatibility (antidotes/safeners) mentioned above under (b) are present per part by weiht of active compound of the formula (I). The active compound combinations accordin to the invention are enerally applied in the form of finished formulations. However, the active compounds contained in the active compound combinations can, as individual formulations, also be mixed durin use, i.e. be applied in the form of tank mixes. For certain applications, in particular by the post-emerence method, it may furthermore be advantaeous to include, as further additives in the formulations, mineral or veetable oils which are compatible with plants (for example the commercial preparation "Rako Binol"), or ammonium salts, such as, for example, ammonium sulfate or ammonium thiocyanate. The novel active compound combinations can be used as such, in the form of their formulations or the use forms prepared therefrom by further dilution, such as ready-to-use solutions, suspensions, emulsions, powders, pastes and ranules. Application is in the customary manner, for example by waterin, sprayin, atomizin, dustin or scatterin. The application rates of the active compound combinations accordin to the invention can be varied within a certain rane; they depend, inter alia, on the weather and on soil factors. In eneral, the application rates are between 0.00 and 5 k per ha, preferably between 0.005 and 2 k per ha, particularly preferably between 0.0 and 0.5 k per ha. The active compound combinations accordin to the invention can be applied before and after emerence of the plants, that is to say by the pre-emerence and post-emerence method. Dependin on their properties, the safeners to be used accordin to the invention can be used for pretreatin the seed of the crop plant (seed dressin) or can be introduced into the seed furrows prior to sowin or be used separately prior to the herbicide or toether with the herbicide, before or after emerence of the plants. Preparation and use of the active compounds accordin to the invention are illustrated in the examples below. Under aron, 5.24 of potassium tert-butoxide-95% pure- (44.4 mmol) are initially chared in 0ml of dimethylacetamide in a 00 ml three-necked flask fitted with thermometer and reflux condenser. At 40 to 50°C, .7 of the compound accordin to Example II-l (20.2 mmol) in 0ml of dimethylacetamide are added dropwise. The mixture is stirred at 60°C for h and monitored by thin-layer chromatoraphy durin this time. The reaction solution is then stirred into 00 ml of ice-water, the pH is adusted to 2 usin cone. HC and the precipitate is filtered off with suction. The product is then purified by column chromatoraphy on silica el (dichloromethane:ethyl acetate 5:3). Yield 7. (94% of theory), m.p. 225.6°C. (3 mmol) of example I-l-c-4 from WO 97/02243 are initially chared in 30 ml of anhydrous tetrahydrofuran in a 00 ml three-necked flask. At -7°C, 2.64 ml of nbutyllithium (2.5m in n-hexane) are added dropwise. After 5 min of stirrin, 0.76 (3 mmol) of iodine in 5 ml of anhydrous tetrahydrofuran is added dropwise at -7°C, and the mixture is allowed to slowly warm to room temperature. The solvent is evaporated and the residue is pre-purified by flash chromatoraphy on silica el usin the mobile phase methylene chloride/acetone 5:. The product-containin fractions were combined, the solvent was removed under reduced pressure and the residue 250 m was purified by reversed-phase chromatoraphy usin acetonitrile/water (radient proram 70:30 -» 0:90). Yield: 40 m (4 2.7% of theory) m.p. 245°C. The followin compounds of the formula (I-l-a) are obtained analoously to example (I-l-a-) and in accordance with the eneral statements on the (Figure Removed) Under an atmosphere of protective as, 0.4 of the compound of example I-l-a-5 is initially chared in 30 ml of ethyl acetate, 0.5 ml of triethylamine and 0 m of Stelich base are added and 0.5 of cyclopropylcarbonyl chloride in 5 ml of ethyl acetate is added dropwise under reflux and the mixture is stirred further under reflux. After the reaction has ended (monitored by thin-layer chromatoraphy) the product is purified by flash column separation on silica el (mobile phase ethyl acetate) Yield: 0.4 (75% of theory), m.p. 67°C The followin compounds of the formula (I-l-b) are obtained analoously to example (I-l-b-) and in accordance with the eneral statements on the Under aron, 0.66 (.5 mmol) of example I-l-a-2 is initially chared in 20ml of anhydrous methylene chloride in a 00 ml three-necked flask, 0.2 ml (.5 mmol) of triethylamine is added and 0.4 ml (.5 mmol) of ethyl chloroformate is added dropwise at 20°C. The mixture is stirred for 4 hours, the solvent is evaporated under reduced pressure and the residue is chromatoraphed on silica el usin the mobile phase methylene chloride/ethyl acetate 0:. Yield: 0.4 (A 43% of theory) m.p. 9°C The followin compounds of the formula (I-l-c) are obtained analoously to example (I-l-c-) and in accordance with the eneral statements on the if-. preparation Under aron, 5. of methyl cis-l-amino-4-methoxycycIohexanecarboxylate hydrochloride (0.0226 mol) are initially chared under aron in 50 ml of anhydrous tetrahydrofuran in a 00 ml three-necked flask fitted with thermometer and reflux condenser. At 20°C, 6.3 ml (0.0452 mol) of triethylamine are added dropwise. The mixture is stirred for 5 min, and 5.4 of 2-iodophenylacetic acid (0.0205 mol) are added at 20°C. After 5 min, 4.3 ml of triethylamine (0.030 mol) are added dropwise, immediately followed by .5 ml of phosphorus oxychloride; the solution should boil ently. The mixture is stirred under reflux for another 30 min. After coolin and removal of the solvent under reduced pressure, the pro'duct is purified by column chromatoraphy on silica el (dichloromethane:ethyl acetate 3:) Yield: .7 (96% of theory), m.p. 52°C . (4.5 mmol) of the compound of example XXIX- in 20 nil of methylene chloride are added dropwise to .4 ml of concentrated sulfuric acid, and the mixture is stirred at an external temperature of 30 - 40°C for 2 hours. 3.3 ml of methanol are then added dropwise, the mixture is stirred at an external temperature of 40 - 70°C for 4 hours, allowed to stand overniht and stirred at 40 to 70°C for a further 3 hours. The reaction solution is then poured onto ice/H2O and extracted with dichloromethane, and the extracts are washed with sat. NaHCC3 solution, dried and concentrated usin a rotary evaporator. (CDC3 300 MHz): S = 7.40 (s, 2H, Ar-H), 3.65 (s, 3H, OCH3), 3.55 (s, 2H, CH2) .90 (sept, lH,CH(CH3)2)ppm. The followin compounds of the formula (II) are obtained analoously to examples (II-l) and (II- 25) and in accordance with the eneral statements on the preparation .7 (5.59mmol) of 4-iodo-2-ethyl-6-methylphenylacetic acid are initially chared in 25ml of tetrahydrofuran, 2 ml of triethylamine and 0.627 (5.59 mmol) of 2-amino-2- methylisobutyronitrile are added, the mixture is stirred at room temperature for 5 minutes, ml of triethylamine is added followed by the dropwise addition of 0.6 ml of phosphorus oxychloride such that the mixture boils ently. The mixture is stirred under reflux for 30 minutes, concentrated on a rotary evaporator and worked up with ethyl acetate/water, and the oranic phase is dried with sodium sulfate, stirred with silica el, filtered off and concentrated usin a rotary evaporator. Yield: .2 (74% of theory), m.p. 6°C of the formula (XXIX) are obtained analoously to example (XXIX-) and in accordance with the eneral statements on the preparation 2-iodophenylacetyl chloride and 0.66 (5 mmol) of ethyl 2-methyl-2-hydroxypropionate are heated at 40°C for 0 h, after coolin, 0 ml of dimethylformamide are added, and 6 ml of M potassium t-butoxide solution (6 mmol) are added dropwise. The mixture is stirred at room temperature for 0 h and concentrated usin a rotary evaporator, and the residue is partitioned between water and ethyl acetate. The aqueous phase is acidifed with 2N HC and the product is extracted with ethyl acetate, the oranic phase is dried and concentrated usin a rotary evaporator. Yield: . (6% of theory) loP .0 The followin compounds of the formula (I-2-a) are obtained analoously to example (I-2-a-l) in accordance with the eneral statements on the preparation 0.25 (0.757mmol) of the compound of example I-2-a-l and 0.092 (0.909 mmol) of triethylamine are initially chared in 0ml of dichloromethane, 0.097 (0.909 mmol) of isobutyryl chloride is added dropwise and the mixture is stirred at room temperature overniht, washed with 0% strenth citric acid and 0% strenth aqueous sodium hydroxide solution, dried and concentrated usin a rotary evaporator. The crude product is purified by column chromatoraphy on silica el (radient dichloromethane dichloromethane/ethyl acetate 95:5). Yield: 0.23 (74% of theory), loP 3.53 The followin compounds of the formula (I-2-b) are obtained analoously to example (I-2-b-l) and in accordance with the eneral statements on the preparation 0.25 (0.757 mmol) of the compound of example I-2-a-l and 0.092 (0.909 mmol) of triethylamine are initially chared in 0 ml of dichloromethane, 0. (0.909 mmol) of isopropyl chloroformate is added dropwise, and the mixture is stirred at room temperature overniht, washed with 0% strenth citric acid and 0% strenth aqueous sodium hydroxide solution, dried and concentrated usin a rotary evaporator. The crude product is purified by column chromatoraphy on silica el (radient dichloromethane dichloromethane/ethyl acetate 95:5). Yield: 0.6 (46% of theory), loP 3.47 The followin compounds of the formula (I-2-c) are obtained analoously to example (I-2-c-) and in accordance with the eneral statements on the preparation 0.566 of potassium tert-butoxide is initially chared in 5 ml of N,N-dimethylacetamide at 50°C, of the compound of example (XII-) in 5 ml of N,N-dimethylacetamide is added and the mixture is stirred at 60°C for 2 h. The cooled reaction solution is then added dropwise to icewater/ concentrated HC. The crystals are filtered off with suction. Yield: 0.54 (6% of theory), m.p. 229°C Example I--b-l 0.25 (0.00 mol) of the compound of example I--a-l and 0.074 of 2-methylpropionyl chloride are initially chared in 5 ml of toluene at room temperature, 0. ml of triethylamine is added 5 dropwise, the mixture is stirred for 2 h, water is added and the mixture is extracted. The oranic phase is dried and concentrated usin a rotary evaporator, and the residue is crystallized usin n-heptane and a little ethyl acetate. Yield: 0. (32% of theory) ]H-NMR (300 MHz, CDC3): 5 = 7.40 ppm (s, 2H, Ar-H), 3.0 ppm (m, 2H, N-CH2), 3.40 ppm 0 (m, 2H,N-CH2), 2.40 ppm (sept, H, CHC(CH3)2), 2.00-.0 ppm (m, 4H, 2 xCH2 cycle). Example No. (I--b-2) is obtained analoously to example (I--b-l) (300 MHz, CDC3): S = 7.40 (s, 2H, Ar-H), 3.90 (m, 2H, N-CH_2), 3.40 (m, 2H, N-CH2), 2.60-2.40 (m, 2H, Ar-CH2) ppm. Example I--c-l 0.07 ml of ethyl chloroformate is added to 0.25 (0.00 mol) of the compound of example I--a-l and 0. ml of triethylamine and 5 ml of toluene, and the mixture is stirred at room temperature for hour. The reaction solution is extracted with water and the oranic phase is dried. Purification is carried out by HPLC. Yield: 0.09 (29% of theory) (300 MHz, CDCI3): 5 = 7.40 (s, 2H, Ar-H), 4.5 (q, 2H, O-CH2), 3.0 (tr, 2H, N-CH2), 3.45 (tr, 2H, Ar-CH2), 2.50 (m, 2H, Ar-CH2), 2.00- .0 (m, 4H, 2 x CH2 .3 ml of triethylamine are added to 2 of 4-iodo-2-ethyl-6-methylphenylacetic acid in 40 ml of tetrahydrofuran, and the mixture is stirred for 5 minutes. .095 of ethyl hexahydropyridazine carbamate are then added, the mixture is stirred for 0 minutes and .92 ml of triethylamine are added. Immediately afterward, 0.55 ml of phosphoryl chloride is slowly added dropwise. The mixture is stirred under reflux for 30 minutes. After coolin, the mixture is concentrated usin a rotary evaporator, the residue is worked up with ethyl acetate/water and the oranic phase is separated off, dried with sodium sulfate, filtered off and concentrated usin a rotary evaporator. Yield: 2.5 (5% of theory) ]H-NMR (400 MHz, CDC3): = .5, .30 (2 t, 6H, OCH2CH3, Ar CH2CH3), 2.20 (s, 3H, Ar-CH3), 2.50 (q, 2H, Ar-CH2CH3), 3.60, 3.70 (2d, 2H, NCH2), 7.40 (s, 2H, Ar-H) ppm. Under aron, a solution of 0 of methyl (4-bromo-2-methyl-6-ethylphenyl)acetate, .056 of sodium iodide, 7.023 of copper(I) iodide and 3.72 of N,N'-dimethylethylenediamine in 250 ml of dioxane is heated at 0°C for h. After the reaction has ended, the reaction mixture filtered and the mother liquor is diluted with 300 ml of water and extracted twice with 200 ml of dichloromethane. The oranic phase is washed with 25% strenth ammonia solution, dried over sodium sulfate and freed from the solvent. Yield of methyl (2-ethyl-4-iodo-6- methylphenyl)acetate: 7. , 65%. 'H-NMR (300MHz, d6-DMSO): 6 = 7.42 (d, H), 7.39 (d, H), 3.6 (s, 2 H), 3.6 (s, 3 H), 2.55 (q, 2 H), 29 (s, 3 H), .0 (t, 3 H) ppm. (Figure Removed) Example XXVII- A solution of 0.696 of LiOH in 50 ml of water is added to a solution of 7.7 of methyl (2-ethyl- 4-iodo-6-methylphenyl)acetate in 50 ml of THF, and the mixture is stirred at room temperature h. The mixture is then evaporated to dryness usin a rotary evaporator, and in each case 50 ml of ethyl acetate and water are added to the residue. The phases are separated and the ethyl acetate phase is washed with water. The combined aqueous phases are adusted to pH = usin HC, and the precipitated solid is filtered off with suction, washed with water and dried under reduced pressure. Yield of (2-ethyl-4-iodo-6-methylphenyl)acetic acid: 6 , 7%. !H-NMR (300MHz, d6-DMSO): = 2.5 (s(br), H), 7.40 (d, H), 7.3 (d, H), 3.57 (s, 2 H), 2.56 (q, 2 H), .09 (t, 3 H) ppm. Example XXXI-2 Under aron, a solution of 20 of methyl (5-bromo-2-methylphenyl)acetate, 24.663 of sodium iodide, 5.66 of copper(I) iodide and 7.075 of N,N'-dimethylethylenediamine in 500ml of dioxane is heated at 0°C for 3 days. Another of sodium, 5.5 of copper(I) iodide and 3.3 of N,N'-dimethylethylenediamine are then added. After a further 3 days of heatin at 0°C, the reaction mixture is filtered and the mother liquor is diluted with 300 ml of water and extracted twice with 200 ml of dichloromethane. The oranic phase is washed with 25% strenth ammonia solution, dried over Na2SO4 and freed from the solvent. Yield of methyl (5-iodo-2- methylphenyl)acetate: .6 , 30%. ]H-NMR (300MHz, d6-DMSO): 5 = 7.56 (d, H), 7.5 (d, H), 6.99 (d, H), 3.62 (s, 2 H), 3.57 (s, 3H),2.6(s,3H)ppm. Example XXVII-2 A solution of .04 of LiOH in 75 ml of water is added to a solution of 0.7 of methyl (5-iodo- 2-methylphenyl)acetate in 75 ml of THF, and the mixture is stirred at room temperature for h. The mixture is then concentrated to dryness usin a rotary evaporator, and in each case 75 ml of ethyl acetate and water are added to the residue. The phases are separated and the oranic phase is washed with water. The combined aqueous phases are adusted to pH = usin HC and the precipitated solid is triturated successively with dichloromethane and ethyl acetate, filtered off (Figure Removed) with suction and dried under reduced pressure. For further purification, it is triturated with diethyl ether and filtered off. Yield of (5-iodo-2-methylphenyl)acetic acid: 5.5 , 44%. (300MHz, d6-DMSO): S = 2.2 (s, (br) H), 7.55 (d, H), 7.49 (d, H), 6.9 (d, H), 3.56 (s, 2H),2.7 (s, 3 H) ppm. The followin compounds of the formula (XXXI) are obtained analoously to examples (XXXI- - The loP values iven in the Tables and Preparation Examples above are determined in accordance with EEC Directive 79/3 Annex V.A by HPLC (Hih Performance Liquid Chromatoraphy) on a reversed-phase column (C ). Temperature: 43°C. The determination is carried out in the acidic rane at pH 2.3 usin the mobile phases 0.% aqueous phosphoric acid and acetonitrile; linear radient from 0% acetonitrile to 95% acetonitrile. The LC-MS determination in the acidic rane is carried out at pH 2.7 usin the mobile phases 0.% aqueous formic acid and acetonitrile (contains 0.% formic acid); linear radient from 0% acetonitrile to 95% acetonitrile. The LC-MS determination in the neutral rane is carried out at pH 7. usin the mobile phases 0.00 molar aqueous ammonium bicarbonate solution and acetonitrile; linear radient from 0% acetonitrile to 95% acetonitrile. Calibration is carried out usin unbranched alkan-2-ones (havin 3 to 6 carbon atoms) with known loP values (determination of the loP values by the retention times usin linear interpolation between two successive alkanones). The lambda max values were determined in the maxima of the chromatoraphic sinals usin the UV spectra from 200 nm to 400 nm. Phaedon Test (Spray treatment) Solvents: 7 parts by weiht of acetone .5 parts by weiht of dimethylformamide Emulsifier: 0.5 part by weiht of alkylaryl polylycol ether To produce a suitable preparation of active compound, part by weiht of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containin water to the desired concentration. Discs of Chinese cabbae (Brassica pekinensis) are sprayed with an active compound preparation of the desired concentration and, after dryin, populated with larvae of the mustard beetle (Phaedon cochleariae). After the desired period of time, the effect in % is determined. 00% means that all beetle larvae have been killed; 0% means that none of the beetle larvae have been killed. In this test, for example, the followin compounds of the Preparation Examples show, at an application rate of 500 /ha, an efficacy of 0%. Myzus Test (Spray treatment) Solvents: 7 parts by weiht of acetone .5 parts by weiht of dimethylformamide Emulsifier: 0.5 part by weiht of alkylaryl polylycol ether To produce a suitable preparation of active compound, part by weiht of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containin water to the desired concentration. Discs of Chinese cabbae (Brassica pekinensis) which are infested by all staes of the reen peach aphid {Myzus persicae) are sprayed with an active compound preparation of the desired concentration. After the desired period of time, the effect in % is determined. 00% means that all aphids have been killed; 0% means that none of the aphids have been killed. In this test, for example, the followin compounds of the Preparation Examples show, at an application rate of 500 /ha, an efficacy of 0%. Nilaparvata luens Test (hydroponic treatment) Solvents: 7 parts by weiht of acetone .5 parts by weiht of dimethylformamide Emulsifier: 0.5 part by weiht of alkylaryl polylycol ether To produce a suitable preparation of active compound, part by weiht of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containin water to the desired concentration. The active compound preparation is pipetted into water. The stated concentration refers to the amount of active compound per volume unit of water (m/ = ppm). After the desired period time, the water is infected with the brown plant hopper (Nilaparvata luens). After the desired period of time, the effect in % is determined. 00% means that all plant hoppers have been killed; 0% means that none of the plant hoppers have been killed. In this test, the compound of Preparation Example I-2-a-2 showed, at a concentration of 20 Tetranychus Test; OP-resistant/spray treatment (TETRUR) Solvents: 7 parts by weiht of acetone .5 parts by weiht of dimethyIformamide Emulsifier: 0.5 part by weiht of alkylaryl polylycol ether To produce a suitable preparation of active compound, part by weiht of active compound is mixed with the stated amounts of solvents and emulsifier, and the concentrate is diluted with emulsifier-containin water to the desired concentration. Discs of bean leaves (Phaseolus vularis) which are heavily infested by all staes of the reenhouse red spider mite (Tetranychus urticae} are sprayed with an active compound preparation of the desired concentration. After the desired period of time, the effect in % is determined. 00% means that all spider mites have been killed; 0% means that none of the spider mites have been killed. In this test, for example, the followin compounds of the Preparation Examples show, at an application rate of 00 /ha, an efficacy of 0%. M-a-2, I-l-a-4, I-l-a-5, I-l-a-7, I-l-a-, I-l-a-2, I-l-a-,-l-a-9, I-l-a-2,-l-a-2,-l-a-22,- l-b-2,I-l-b-,-l-c-,-l-c-4,-l-c-5,-l-c-20,-2-a-6,-2-b-2,-2-b-5,-2-b-6, -2 b-,-2-b-0, I-2-b-ll, I-2-C-2,-2-C-3, I-2-C-4,-2-c-S, I--b-l, I--b-2. In this test, for example, the followin compound of the Preparation Example showed, at an application rate of 500 /ha, an efficacy of 0%: Herbicidal pre-emerence action Seeds of monocotyledonous and dicotyledonous weed and crop plants are placed in sandy loam in wood fiber pots and covered with soil. The test compounds, formulated in the form of wettable powders (WP) or as emulsion concentrates (EC), are then, as an aqueous suspension with a water application rate of 00 /ha (converted), with 0.2% of wettin aent added, applied to the surface of the coverin soil. After the treatment, the pots are placed in a reenhouse and kept under rowth conditions for the test plants. The visual assessment of the emerence damae on the test plants is carried out after a trial period of 3 weeks by comparison with untreated controls (herbicidal effect in percent (%): (Figure Removed) 00% effect = the plants have died, 0% effect = like control plants). Here, the followin compounds, for example, controlled Avena sativa, Lolium multiflorum and Setaria viridis at an application rate of 320 /ha with 70% efficacy: I-l-a-,-l-a-4,-l-a-2,-l-b-7. - 94- Example F Herbicidal post-emerence action Seeds of monocotyledonous and dicotyledonous weed and crop plants are placed in sandy loam in wood fiber pots, covered with soil and cultivated in a reenhouse under ood rowth conditions. Two to three weeks after sowin, the test plants are treated at the one-leaf stae. The test compounds, formulated as wettable powders (WP) or as emulsion concentrates (EC), are then, as an aqueous suspension with a water application rate of 00 /ha (converted), with 0.2% of wettin aent added, sprayed onto the reen parts of the plants. After the test plants have been kept in the reenhouse under optimum rowth conditions for about 3 weeks, the effect of the preparations is rated visually in comparison to treated controls (herbicidal effect in percent (%): 00% effect = the plants have died, 0% effect = like control plants). Here, the followin compounds, for example, controlled Avena sativa, Echinochloa crus-alli, Lolium multiflorum and Setaria viridis at an application rate of 320 /ha with 70% efficacy: I-l-a-, I-l-a-n, I-l-a-2, I-l-a-3, I-l-a-4, I-l-a-2, I-l-c-, I-l-c-6, I-l-c-, I-l-c-2,-2-b-0, I-2-C-3,--b-2. Example Herbicidal post-emerence action Seeds of monocotyledonous and dicotyledonous weed and crop plants are placed into sandy loam in wood fiber pots or in plastic pots, covered with soil and cultivated in a reenhouse, durin the veetation period also outdoors outside of the reenhouse, under ood rowth conditions. Two to three weeks after sowin, the test plants are treated at the one- to three-leaf stae. The test compounds, formulated as wettable powders (WP) or liquid (EC), are, in various dosaes at a water application rate of 300 /ha (converted), with wettin aent (0.2 to 0.3%) added, sprayed onto the plants and the surface of the soil. Three to four weeks after the treatment of the test plants, the effect of the preparations is rated visually in comparison to treated controls (herbicidal effect in %) (%): 00% effect = the plants have died, 0% effect = like control plants). Use of safeners If it is additionally to be tested as to whether safeners can improve the plant compatibility of test substances in the case of crop plants, the followin options are used for applyin the safener: seeds of the crop plants are, before sowin, dressed with the safener substance (the amount of safener stated in percent, based on the weiht of the seed) before the application of the test substances, the crop plants are sprayed with the safener at a certain application rate per hectare (usually day before the application of the test substances) the safener is applied toether with the test substance as a tank mix (the amount of safener is stated in /ha or as a ratio, based on the herbicide). By comparin the effect of test substances on crop plants without or with safener treatment, it is possible to assess the effect of the safener substance. Container trials with cereal in a reenhouse Mefenpyr day prior to herbicide application (Figure Removed) Critical concentration test/Soil insects - Treatment of transenic plants Test insect: Diabrotica balteata - larvae in the soil Solvent: 7 parts by weiht of acetone Emulsifier: part by weiht of alkylaryl polylycol ether To produce a suitable preparation of active compound, part by weiht of active compound is mixed with the stated amount of solvent, the stated amount of emulsifier is added and the concentrate is diluted with water to the desired concentration. The preparation of active compound is poured onto the soil. Here, the concentration of active compound in the preparation is virtually immaterial; only the amount by weiht of active compound per unit volume of soil, which is stated in ppm (m/), matters. The soil is filled into 0.25 pots, and these are allowed to stand at 20°C. Immediately after the preparation, 5 preerminated corn rains of the cultivar YIELD UARD (trademark of Monsanto Comp., USA) are placed into each pot. After 2 days, the appropriate test insects are placed into the treated soil. After a further 7 days, the efficacy of the active compound is determined by countin the corn plants that have emered ( plant = 20% activity). Example I Heliothis virescens test - treatment of transenic plants Solvent: 7 parts by weiht of acetone Emulsifier: part by weiht of alkylaryl polylycol ether To produce a suitable preparation of active compound, part by weiht of active compound is mixed with the stated amount of solvent and the stated amount of emulsifier, and the concentrate diluted with water to the desired concentration. Soybean shoots (lycine max) of the cultivar Roundup Ready (trademark of Monsanto Comp. USA) are treated by bein dipped into the preparation of active compound of the desired concentration and are populated with the tobacco budworm Heliothis virescens while the leaves are still moist. After the desired period of time, the k i l l of the insects is determined. Claims A compound of the fomula (1) (Figure Removed)in whichepesents iodine,X epesents hydogen, alkyl, halogen, haloalkyl, alkoxy o haloalkoxy,Y epesents hydogen, alkyl, halogen o alkoxy, with the poviso that at least one of the adicals 2, X o Y is located in the 2-position of the phenyl adical and is not hydogen,CKE epesents one of the goupsepesents hydogen, in each case optionally halogen-substituted alkyl,alkenyl, alkoxyalkyl, alkylthioalkyl, satuated o unsatuated, optionallysubstituted cycloalkyl in which optionally at least one ing atom is eplaced by a heteoatom, o in each case optionally halogen-, alkyl-,haloalkyl-, alkoxy-, haloalkoxy-, cyano- o nito-substituted ayl, aylalkylo hetayl,epesents hydogen, alkyl o alkoxyalkyl, oA and B togethe with the cabon atom to which they ae attached epesent a satuated o unsatuated, unsubstituted o substituted cycle whichoptionally contains at least one heteoatom,D epesents hydogen o an optionally substituted adical fom the goup consisting of alkyl, alkenyl, alkynyl, alkoxyalkyl, satuated o unsatuated cycloalkyl in which optionally one o moe ing membes ae eplaced by heteoatoms, aylalkyl, ayl,i hetaylalkyl o hetayl o A and D togethe with the atoms to which they ae attached epesent a satuated o unsatuated cycle which is unsubstituted o substituted in the A,D moiety and optionally contains at least one (in the case of CKE=g one futhe) heteoatom, o A and ' togethe epesent alkanediyl o alkenediyl, optionally substituted by hydoxyl, in each case optionally substituted alkyl, alkoxy, alkylthio, cycloalkyl, benzyloxy o ayl o epesents hydogen o alkyl, epesents hydogen, epesents optionally substituted alkyl, alkoxyalkyl, alkylthioalkyl, optionally substituted cycloalkyl (in which optionally one methylene goup is eplaced by oxygen o sulfu) o optionally substituted phenyl, otogethe with the cabon atom to which they ae attached epesent a satuated o unsatuated, unsubstituted o substituted cycle which optionally contains a heteoatom, g epesents hydogen (a) o epesents one of the goups (Figure Removed) E epesents a metal ion euivalent o an ammonium ion, L epesents oxygen o sulfu, M epesents oxygen o sulfu, ' epesents in each case optionally halogen-substituted alkyl, alkenyl, alkoxyalkyl, alkylthioalkyl, polyalkoxyalkyl o optionally halogen-, alkyl- o alkoxy-substituted cycloalkyl which may be inteupted by at least one heteoatom, in each case optionally substituted phenyl, phenylalkyl, hetayl, phenoxyalkyl o hetayloxyalkyl, 2 epesents in each case optionally halogen-substituted alkyl, alkenyl, alkoxyalkyl, polyalkoxyalkyl o epesents in each case optionally substituted cycloalkyl, phenyl o benzyl, , and - independently of one anothe epesent in each case optionally halogen-substituted alkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkenylthio, cycloalkylthio o epesent in each case optionally substituted phenyl, benzyl, phenoxy o phenylthio, .6 and 7 independently of one anothe epesent hydogen, in each case optionally halogen-substituted alkyl, cycloalkyl, alkenyl, alkoxy, alkoxyalkyl, epesent optionally substituted phenyl, epesent optionally substituted benzyl, o togethe with the N atom to which they ae attached epesent a cycle which is optionally inteupted by oxygen o sulfu. 2. The compound of the fomula (1) as claimed in claim i in which epesents iodine, with the poviso that at least one of the adicals 2, X o Y is located in the 2-position of the phenyl adical and is not hydogen, CKE epesents one of the goups (Figure Removed) A epesents hydogen o in each case optionally halogen-substituted C B epesents hydogen, A, B and the cabon atom to which they ae attached epesent satuated o unsatuated in which optionally one ing membe is eplaced by oxygen o sulfu and which ae optionally mono- o disubstituted by alkylthio, halogen o phenyl o A, B and the cabon atom to which they ae attached epesent -cycloalky! which is substituted by an alkylenedithiol goup o by an alkylenedioxyl goup o by an alkylenediyl goup which optionally contains one o two not diectly ad2acent oxygen and/o sulfu atoms and which is optionally substituted by -alkyl, which goup, togethe with the cabon atom to which it is attached, foms a futhe five- to eight-membeed ing, o A, B and the cabon atom to which they ae attached in which two substituents togethe with the cabon atoms to which they ae attached epesent in each case optionally o halogen- in which optionally one methylene goup is eplaced by oxygen o D epesents hydogen, in each case optionally halogen-substituted C which optionally one ing membe is eplaced by oxygen o sulfu o in each case cyano- o nito-substituted phenyl, hetayl having 5 o 6 ing atoms, phenyl--alkyl o hetayl- -alkyl having 5 o 6 ing atoms o A and D togethe epesent in each case optionally substituted C3-C5-alkanediyl o C3-C6- alkenediyl in which optionally one methylene goup is eplaced by a cabonyl goup, oxygen o sulfu, possible substituents being in each case: halogen, hydoxyl, mecapto o in each case optionally halogen-substituted C\- benzyloxy, o a futhe C3-Cg-alkanediyl gouping, C3-C6-alkenediyl gouping o a butadienyl gouping which is optionally substituted by -alkyl o in which optionally two ad2acent substituents togethe with the cabon atoms to which they ae attached fom a futhe satuated o unsatuated cycle having 5 o 6 ing atoms (in the case of the compound of the fomula (i-i) A and D in this case togethe with the atoms to which they ae attached epesent, fo example, the goups AD-i to AD- 10 mentioned futhe below) that may contain oxygen o sulfu o which optionally contains one of the following goups (Figure Removed) A and ' togethe epesent C3-C5-alkanediyl o C4-C3-alkenediyl, each of which is optionally mono- o disubstituted by identical o diffeent substituents fom the goup consisting of halogen; hydoxylC3-C7-cycloalkyl, each of which is optionally mono- to tisubstituted byidentical o diffeent halogen substituents; and benzyloxy o phenyl, each of which is optionally mono- to tisubstituted by identical o diffeent substituents fom the goup consisting of halogen, o CC-alkenediyl futhemoe optionally contains one of the goups below (Figure Removed) E epesents a metal ion euivalent o an ammonium ion, L epesents oxygen o sulfu and M epesents oxygen o sulfu. optionally one cabon atom is eplaced by oxygen o sulfu, epesents hydogen, epesents in each case optionally halogen-substituted and a independently of one anothe epesent hydogen, epesent optionally halogen-substituted and a togethe with the cabon atom to which they ae attached epesent a 3. The compound of the fomula (1) as claimed in claim i in which 2 epesents iodine, X epesents hydogen, fluoine, chloine, bomine, iodine, Y epesents hydogen, fluoine, chloine, bomine, iodine, with the poviso that at least one of the adicals 2, X o Y is located in the 2-position of the phenyl adical and is not hydogen, A epesents hydogen, epesents of which is optionally mono- to tisubstituted by fluoine o chloine, epesents -cycloalkyl which is optionally mono- to disubstituted by C2-C2-alkoxy o (but not in the case of the compounds of the fomulae (i-3), (i-4), (i-6) and (i-7)) epesents phenyl o benzyl, each of which is optionally mono- to disubstituted by fluoine, chloine, bomine, C4-alkoxy, C1C2-haloalkoxy, cyano o nito, B epesents hydogen, C2-Calkyl o CpCa-alkoxy-CpC2-alkyl, o A, B and the cabon atom to which they ae attached epesent satuated o unsatuated C5-C7-cycloalkyl in which optionally one ing membe is eplaced by oxygen o sulfu and which is optionally mono- to disubstituted by tifluoomethyl, C2-Cg-alkoxy o C2-alkoxy-C2-alkoxy, with the poviso that in this paticulaly pefeably epesents hydogen o methyl, o A, B and the cabon atom to which they ae attached epesent C5-C6-cycloalkyl which is substituted by an alkylenedithiol goup o by an alkylenedioxyl goup o by an alkylenediyl goup which optionally contains one o two not diectly ad2acent oxygen o sulfu atoms and which is optionally substituted by methyl o ethyl, which goup togethe with the cabon atom to which it is attached foms a futhe five- o six-membeed ing, with the poviso that in this case paticulaly pefeably epesents hydogen o methyl, A, B and the cabon atom to which they ae attached epesent C3-Cg-cycloalkyl o 05- Cg-cycloalkenyl in which two substituents togethe with the cabon atoms to which they ae attached epesent in each case optionally C2-C2-alkyl- o C2-C2- alkoxy-substituted C2-C4-alkanediyl, C2-C4-alkenediyl o butadienediyl, with the poviso that in this case epesents hydogen o methyl, D epesents hydogen, epesents C2-Cg-alkyl, C3-C6-alkenyl, C2-C4-alkoxy-C2- C3-alkyl, each of which is optionally mono- to tisubstituted by fluoine, epesents C3-Cg-cycloalkyl which is optionally mono- to disubstituted by C\-C- alkyl, C2-C4-alkoxy o -haloalkyl and in which optionally one methylene goup is eplaced by oxygen o (but not in the case of the compounds of the fomulae (i-l)) epesents phenyl o pyidyl, each of which is optionally mono- to disubstituted by fluoine, chloine, bomine, C1-C4-alkyl, C2-C4-haloalkyl, C2- C4-alkoxy o C|-C4-haloaikoxy, o A and D togethe epesent optionally mono- to disubstituted C3-C5-alkanediyl in which one methylene goup may be eplaced by a cabonyl goup (but not in the case of the compounds of the fomula (i-l)), oxygen o sulfu, possible substituents being C1-C2-alkyl o C1-C2-alkoxy, o A and D (in the case of the compounds of the fomula (i-l)) togethe with the atoms to which they ae attached epesent one of the goups AD-i to AD-10: A and togethe epesent C3-C4alkanediyl which is optionally mono- o disubstituted by identical o diffeent substituents selected fom the goup consisting of C-C2- alkyl and C2-C2-alkoxy, o ! epesents hydogen, 2 epesents hydogen, % C and " independently of one anothe epesent hydogen o C2-C2-alkyl, epesents hydogen, C1-C4-alkyl, o C3-C6-cycloalkyl which is optionally monoto disubstituted by methyl o methoxy, o -3 and togethe with the cabon to which they ae attached epesent an optionally C2- C2-alkyl- o C1-C2-aikoxy-substituted satuated C5-Cg-ing in which optionally one ing membe is eplaced by oxygen o sulfu, with the poviso that in this case A epesents hydogen o methyl, g epesents hydogen (a) o epesents one of the goups E epesents a metal ion euivalent o an ammonium ion, L epesents oxygen o sulfu and M epesents oxygen o sulfu, i epesents C2-Cg-alkyl, C2-C1g-alkenyl, C \ -C4-alkoxy-C 2 -C2-alkyl, C2-C alkylthio-C2-C2-alkyl, each of which is optionally mono- to tisubstituted by fluoine o chloine, o C3-C6-cycloalkyl which is optionally mono- to disubstituted by fluoine, chloine, C1-C2-alkyl o C1-C2-alkoxy and in which optionally one o two not diectly ad2acent ing membes ae eplaced by oxygen, epesents phenyl which is optionally mono- to disubstituted by fluoine, chloine, bomine, cyano, nito, C1-C4-alkyl, C2-Calkoxy, C1-C2-haloalkyl o C2 haloalkoxy, 2 epesents C2-Cg-alkyl, C-Cg-alkenyl o C1-C4-alkoxy-C2-C4-alkyl, each of which is optionally mono- to tisubstituted by fluoine, epesents C3-Cg-cycloalkyl which is optionally monosubstituted by C2-C2-aikyl o C1-C2-alkoxy o epesents phenyl o benzyl, each of which is optionally mono- to disubstituted by fluoine, chloine, bomine, cyano, nito, C2-C4-alkyl, C2-C3-alkoxy, tifluoomethyl o tifluoomethoxy, - epesents C2-C-alkyl which is optionally mono- to tisubstituted by fluoine o epesents phenyl which is optionally monosubstituted by fluoine, chloine, bomine, C2-C/2-alkyl, C1-g4-alkoxy, tifluoomethyl, tifluoomethoxy, cyano o nito, epesents C1-C5-alkyl, C2-Cg-alkoxy, C2-Cg-alkylamino, dKC2-Cg-alkyOamino, C1-C6-alkylthio, C3-C4-alkenylthio, C3-C6-cycloalkylthio o epesents phenyl, phenoxy o phenylthio, each of which is optionally monosubstituted by fluoine, chloine, bomine, nito, cyano, C1-C3-alkoxy, C1-C3-haloalkoxy, C2-C3- alkylthio, C1-C3-haioalkylthio, C2-C3-alkyl o tifluoomethyl, epesents C i -C6-alkoxy o C i -C6-alkylthio, epesents hydogen, C2-Cg-alkyl, C3-Cg-cycloalkyl, C i -Cg-alkoxy, C1-C6-alkoxy-C1-C4-alky1 epesents phenyl which is optionally monosubstituted by fluoine, chloine, bomine, tifluoomethyl, C2-C4-alkyl o C2-C4-alkoxy, epesents benzyl which is optionally monosubstituted by fluoine, chloine, bomine, C1-C4-alkyl, tifluoomethyl o C 2 -C4-aikoxy, epesents C|-C6-alkyl, C.C6-alkenyl o C|-C6-alkoxy-C1-C4-alkyl, and togethe epesent an optionally methyl- o ethyl-substituted C4-C5-alkylene adical in which optionally one methylene goup is eplaced by oxygen o sulfu. 4. The compound of the fomula (1) as claimed in claim i in which 2 epesents iodine, X epesents hydogen, fluoine, chloine, bomine, methyl, ethyl, popyl, methoxy o ethoxy, Y epesents hydogen, chloine, bomine, methyl, ethyl, popyl o methoxy, with the poviso that at least one of the adicals 2, X o Y is located in the 2-position of the phenyl adical and is not hydogen, CKE epesents one of the goups A epesents hydogen, epesents C2-Calkyl o C1-C2-alkoxy-C1-C2-alkyl, each of which is optionally mono- to tisubstituted by fluoine, epesents cyclopopyl, cyclopentyl o cyclohexyl and, only in the case of the compounds of the fomula (i-5), epesents phenyl which is optionally mono- to disubstituted by fluoine, chloine, bomine, methyl, ethyl, n-popyl, isopopyl, methoxy, ethoxy, tifluoomethyl, tifluoomethoxy, cyano o nito, B epesents hydogen, methyl o ethyl, o A, B and the cabon atom to which they ae attached epesent satuated C$-Cficycloalkyl in which optionally one ing membe is eplaced by oxygen o sulfu and which is optionally monosubstituted by methyl, ethyl, popyl, isopopyl, tifluoomethyl, methoxy, ethoxy, popoxy, methoxyethoxy, butoxy o ethoxyethoxy, with the poviso that in this case C epesents hydogen, o A, B and the cabon atom to which they ae attached epesent Cg-cycloalkyl which is optionally substituted by an alkylenedioxyl goup which contains two not diectly ad2acent oxygen atoms, with the poviso that in this case vey paticulaly pefeably epesents hydogen, o A, B and the cabon atom to which they ae attached epesent C5-Cg-cycloalkyl o 05- C-cycloalkenyl in which two substituents togethe with the cabon atoms to which they ae attached epesent C2-C4-alkanediyl o C2-C4-alkenediyl o butadienediyl, with the poviso that in this case - epesents hydogen, D epesents hydogen, epesents C1-C4-alkyl, C3-C4-alkenyl, C2-C4-alkoxy-C2- C3-alkyl, each of which is optionally mono- to tisubstituted by fluoine, epesents cyclopopyl, cyclopentyl o cyclohexyl o (but not in the case of the compounds of the fomulae (i-i)) epesents phenyl o pyidyl, each of which is optionally monosubstituted by fluoine, chloine, methyl, ethyl, n-popyl, isopopyl, methoxy, ethoxy o tifluoomethyl, o A and D togethe epesent C3-C5-alkanediyl which is optionally monosubstituted by methyl o methoxy and in which optionally one cabon atom is eplaced by oxygen o sulfu o epesent the goup AD-1 A and ' togethe epesent C3-C4-alkanediyl which is optionally mono- o disubstituted by methyl o methoxy, o ! epesents hydogen, epesents hydogen, and independently of one anothe epesent hydogen o methyl, epesents hydogen, methyl, ethyl o popyl, o and togethe with the cabon to which they ae attached epesent a satuated €5- C6-ing which is optionally monosubstituted by methyl o methoxy, with the poviso that in this case A epesents hydogen, g epesents hydogen (a) o epesents one of the goups L epesents oxygen o sulfu, M epesents oxygen o sulfu and E epesents an ammonium ion, i epesents C2-Cg-alkyl, C2-C17-alkenyl, C2-alkoxy-C2-alkyl, C1-C2- alkylthio-C1-alkyl, each of which is optionally monosubstituted by chloine, o epesents cyclopopyl o cyclohexyl, each of which is optionally monosubstituted by fluoine, chloine, methyl o methoxy, epesents phenyl which is optionally monosubstituted by fluoine, chloine, bomine, cyano, nito, methyl, methoxy, tifluoomethyl o tifluoomethoxy, .2 epesents C1-Cg-alkyl, C2C6-alkenyl o C2-C4-alkoxy-C2-C3-alkyl, each of which is optionally monosubstituted by fluoine, o epesents phenyl o ben2yl, 3 epesents C|-Cg-alkyi. 5. The compound of the fomula (1) as claimed in claim i in which 2 epesents iodine, X epesents hydogen, chloine, methyl o ethyl, Y epesents hydogen, chloine, methyl o ethyl, with the poviso that at least one of the adicals 2, X o Y is located in the 2-position of the phenyl adical and is not hydogen, whee the adicals 2, X and Y with thei meanings ae aanged in the following phenyl substitution pattens epesents C|-Chalky i o cyclopopyl, epesents hydogen o methyl, A, B and the cabon atom to which they ae attached epesent satuated Csin which optionally one ing membe is eplaced by oxygen and which is optionally monosubstituted by methyl, methoxy o popoxy, A and D epesent the goup AD-1 in the case of CKE = goup (g) A and D togethe epesent C3-C5-alkanediyl, g epesents hydogen (a) o epesents one of the goups .i epesents C|-C6-alkyl, CC2-alkoxy-C|-alkyl, cyclopopyl, each of which is optionally monosubstituted by chloine, o epesents phenyl which is optionally monosubstituted by chloine, .2 epesents C2-Cg-alkyl C2-Cg-alkenyl o benzyl. A pocess fo pepaing compounds of the fomula (1) as claimed in claim 1 wheein, to obtain (Figue Removed) epesents alkyl ae condensed intamoleculaly in the pesence of a diluent and in the pesence of a base, (B) compounds of the fomula (i-2-a) (Figue Removed)A, B, 2, X , Y and ae as defined above ae condensed intamoleculaly in the pesence of a diluent and in the pesence of a base, (C) compounds of the fomula (i-3-a) in which A, B, 2, X and Y ae as defined above, compounds of the fomula (iV) A, B, 2, X, Y and % ae as defined above and V epesents hydogen, halogen, alkyl o alkoxy, ae cyclized intamoleculaly, if appopiate in the pesence of a diluent and in the pesence of an aC1d, (D) compounds of the fomula (i-4-a) 2, X and Y ae as defined above and Hal epesents halogen, if appopiate in the pesence of a diluent and if appopiate in the pesence of an aC1d accepto, (E) compounds of the fomula (i-5-a) A, 2, X and Y ae as defined above, compounds of the fomula (Vii) in which A is as defined above ae eacted with compounds of the fomula (Vi) Hal, 2, X and Y ae as defined above, if appopiate in the pesence of a diluent and if appopiate in the pesence of an aC1d accepto, (F) compounds of the fomula (i-6-a) in which A, B, l, , 2, X and Y ae as defined above and ° epesents alkyl ae cyclized intamoleculaly, if appopiate in the pesence of a diluent and in the pesence of a base, (g) compounds of the fomula (i-7-a) A, B, 2, 3, 4, 5, 6, X and Y ae as defined above, compounds of the fomula (iX) A, B, 2, 3, 4, 5, 6, X and Y ae as defined above and ° epsents alkyl ae condensed intamoleC1ilaly in the pesence of a diluent and in the pesence of a base, (H) compounds of the fomula (i-g-a) A, D, 2, X and Y ae as defined above, compounds of the fomula (X) A and D ae as defined above a) ae eacted with compounds of the fomula (Vi) (Figue Removed) Hal, X, Y and 2 ae as defined above, if appopiate in the pesence of a diluent and if appopiate in the pesence of an aC1d accepto, B) ae eacted with compounds of the fomula (Xi) 2, X and Y ae as defined above and U epesents NH2 o O-g, whee g is as defined above, if appopiate in the pesence of a diluent and if appopiate in the pesence of a base, o y) ae eacted with compounds of the fomula (Xii) A, D, 2, X, Y and ae as defined above, if appopiate in the pesence of a diluent and if appopiate in the pesence of a base, (1) compounds of the fomulae (i-!-b) to (i-g-b) shown above in which A, B, D, 2, , 2, 3, O4, 5, 6, 1 X, and Y ae as defined above, compounds of the fomulae (i-i-a) to (i-g-a) shown above in which A, B, D, 2, 1 2, 3, 4, 5, ", X and Y ae as defined above ae in each case (a) eacted with aC1d halides of the fomula (Xiii) (B) eacted with caboxylic anhydides of the fomula (XiV) '-CO-O-CO-i (XiV) in which ! is as defined above, if appopiate in the pesence of a diluent and if appopiate in the pesence of an aC1d binde, (2) compounds of the fomulae (i-l-c) to (i-g-c) shown above in which A, B, D, 2, , 2, 3, O4, 5, 6, 2, M, X and Y ae as defined above and L epesents oxygen, compounds of the fomulae (i-l-a) to (i-g-a) shown above in which A, B, D, 2, l, 2, 3, 4, 5, 6? x and Y ae as defined above ae in each case eacted with chloofomic estes o chloofomic thioestes of the fomula (XV) 2-M-CO-C1 (XV) in which 2 and M ae as defined above, if appopiate in the pesence of a diluent and if appopiate in the pesence of an aC1d binde, (K) compounds of the fomulae (i-l-c) to (i-g-c) shown above in which A, B, D, 2, , 2, 3, 4, 5, 6, 2, M, X and Y ae as defined above and L epesents sulfu, compounds of the fomulae (i-l-a) to (i-g-a) shown above in which A, B, D, 2, , 2, O3, O4. , , X and Y ae as defined above ae in each case eacted with chloomonothiofomic estes o chloodithiofomic estes of the fomula (XVi) M and 2 ae as defined above, if appopiate in the pesence of a diluent and if appopiate in the pesence of an aC1d binde, (L) compounds of the fomulae (i-l-d) to (i-g-d) shown above in which A, B, D, 2, , 2, 3, 4, 5, 6, 3, X and Y ae as defined above, compounds of the fomulae (i-l-a) to (i-g-a) shown above in which A, B, D, 2, 1 2, 3, 4, 5, , X and Y ae as defined above ae in each case eacted with sulfonyl chloides of the fomula (XVii) (Figue Removed) is as defined above, if appopiate in the pesence of a diluent and if appopiate in the pesence of an aC1d binde, (M) compounds of the fomulae (i-l-e) to (i-g-e) shown above in which A, B, D, 2, L, 1 2, 3, 4, 5, 6, 4, 5, X and Y ae as defined above, compounds of the fomulae (i-l-a) to (i-g-a) shown above in which A, B, D, 2, 1 2, 3, 4, 5, ", X and Y ae as defined above ae in each case eacted with phosphous compounds of the fomula (XViii) L, 4 and ae as defined above and Hal epesents halogen, if appopiate in the pesence of a diluent and if appopiate in the pesence of an aC1d binde, (N) compounds of the fomulae (i-l-f) to (i-g-f) shown above in which A, B, D, E, 2, , 2, 3, 4, , 6, x and Y ae as defined above, compounds of the fomulae (i-l-a) to (i-g-a) in which A, B, D, 2, 1 2, 3, 4, 5, 6, X and Y ae as defined above ae in each case eacted with metal compounds o amines of the fomulae (XiX) o (XX) t epesents the numbe i o 2 and .10, ! ', '2 independently of one anothe epesent hydogen o alkyl, if appopiate in the pesence of a diluent, compounds of the fomulae (i-l-g) to (i-g-g) shown above in which A, B, D, 2, L, 1 2, 3, 4, 5, 6, 6, 7 X and Y ae as defined above, compounds of the fomulae (i-l-a) to (i-g-a) shown above in which A, B, D, 2, 1 2, 3, 4, 5, , X and Y ae as defined above ae in each case (a) eacted with isocyanates o isothiocyanates of the fomula (XXi) .6 and L ae as defined above, if appopiate in the pesence of a diluent and if appopiate in the pesence of a catalyst, o (6) eacted with cabamoyl chloides o thiocabamoyl chloides of the fomula (XXii) L, .6 and 7 ae as defined above, if appopiate in the pesence of a diluent and if appopiate in the pesence of an aC1d binde,compounds of the fomulae (i-i-a) to i-g-a) shown above in which A, B, D, 2, 1 2, 3, 4, 5, 6, X and Y ae as defined above, compounds of the fomulae (i-i- a') to (i-g-ai) in which A, B, D, 1 2, 3, 4, 5, 6, X and Y ae as defined above and W epesents bomine a) ae eacted with metal iodides, if appopiate in the pesence of a diluent, a Cu(1) salt and a base, o B) ae sub2ected to a halogen/metal exchange with metal oganyls and the anion fomed is uenched with iodinating agents. 7. The use of compounds of the fomula (1) as claimed in claim i fo pepaing pestiC1des and/o hebiC1des. g. A pestiC1de and/o hebiC1de which compises at least one compound of the fomula (1) as claimed in claim i. 9. A method fo contolling animal pests and/o unwanted vegetation which compises allowing compounds of the fomula (1) as claimed in claim i to act on pests and/o thei habitats. 10. The use of compounds of the fomula (1) as claimed in claim i fo contolling animal pests and/o unwanted vegetation. ii. A pocess fo pepaing pestiC1des and/o hebiC1des which compises mixing compounds of the fomula (1) as claimed in claim i with extendes and/o sufactants. i2. A composition compising an effective amount of an active compound combination compising, as components, (ai) at least one substituted cyclic ketoenol of the fomula (1) in which CKE, 2, X and Y ae as defined above and (bi) at least one cop plant compatibility-impoving compound fom the following goup of compounds: 4-dichlooacetyl-l-oxa-4-azaspio[4.5idecane (AD-67, MON-4660), i-dichlooacetylhexahydo- 3,3,ga-timethylpyplo[l,2-aipyimidin-6(2H)-one (dicyclonon, BAS-145i3g), 4-dichlooacetyl-3,4-dihydo-3-methyl-2H-l,4-benzoxazine (benoxaco), i -methylhexyl 5-chloouinoline-g-oxyacetate (clouintocet-mexyl - cf. also elated compounds in EP-A-g6750, EP-A-94349, EP-A-i9i736, EP-A-492366), 3-(2-chloobenzyi)-l-(l-methyll- phenylethyl)uea (cumyluon), a-(cyanomethoximino)phenylacetonitile (cyometinil), 2,4-dichloophenoxyacetic aC1d (2,4-D), 4-(2,4-dichloophenoxy)butyic aC1d (2,4-DB), i-(i-methyl-l-phenylethyl)-3-(4-methylphenyl)uea (daimuon, dymon), 3,6-dichloo- 2-methoxybenzoic aC1d (dicamba), S-l-methyl-i-phenylethyl pipeidine-i-thiocaboxylate (dimepipeate), 2,2-dichloo-N-(2-oxo-2-(2-popenylamino)ethyl)-N-(2-popenyl)- acetamide (DKA-24), 2,2-dichloo-N,N-di-2-popenylacetamide (dichlomid), 4,6-dichloo-2-phenylpyimidine (fencloim), ethyl l-(2,4-dichloophenyl)-5- tichloomethyl-lH-l,2,4-tiazole-3-caboxylate (fenchloazole-ethyl - cf. also elated compounds in EP-A-i74562 and EP-A-346620), phenylmethyl 2-chloo-4- tifluoomethylthiazole-5-caboxylate (fluazole), 4-chloo-N-(l,3-dioxolan-2-ylmethoxy)- a-tifluooacetophenone oxime (fluxofenim), 3-dichlooacetyl-5-(2-fuanyl)-2,2- dimethyloxazolidine (fuilazole, MON-i3900), ethyl 4,5-dihydo-5,5-diphenyl-3- isoxazolecaboxylate (isoxadifen-ethyl - cf. also elated compounds in WO-A-95/07g97), l-(ethoxycabonyl)ethyl 3,6-dichioo-2-methoxybenzoate (lactidichlo), (4-chloo-otolyloxy) acetic aC1d (MCPA), 2-(4-chloo-o-tolyloxy)popionic aC1d (mecopop), diethyl i- (2,4-dichoophenyl)-4,5-dihydo-5-methyl-lH-pyazoie-3,5-dicaboxyiate (mefenpydiethyl - cf. also elated compounds in WO-A-9i/07g74), 2-dichloomethyl-2-methyl-13- dioxolane (Mg-i9i), 2-popenyl-l-oxa-4-azaspio[4.5idecane-4-cabodithioate (Mg-g3g), 1g-naphthalic anhydide, a-(l,3-dioxolan-2-ylmethoximino)phenylacetonitile (oxabetinil), 2,2-dichloo-N-( 13-dioxolan-2-ylmethyl)-N-(2-popenyl)acetamide (PPg-i292), 3-dichlooacetyl-2,2-dimethyloxazolidine (-2g725), 3-dichlooacetyl- 2,2,5-timethyloxazolidine (-2914g), 4-(4-chloo-o-tolyl)butyic aC1d, 4-(4-chloophenoxy) butyic aC1d, diphenylmethoxyacetic aC1d, methyl diphenylmethoxyacetate, ethyl diphenylmethoxyacetate, methyl l-(2-chloophenyl)-5-phenyl-lH-pyazole-3-caboxylate, ethyl l-(2,4-dichloophenyl)-5-methyl-lH-pyazole-3-caboxylate, ethyl l-(2,4-dichloophenyl)- 5-isopopyl-l H-pyazole-3-caboxylate, ethyl l-(2,4-dichloophenyl)-5-(l,l-di- 233- methylethyl)-! H-pyazole-3-caboxylate, ethyl l-(2,4-dichloophenyl)-5-phenyllH- pyazole-3-caboxylate (cf. also elated compounds in EP-A-269g06 and EP-A-333i3i), ethyl 5-(2,4-dichloobenzyl)-2-isoxazoline-3-caboxylate, ethyl 5-phenyl- 2-isoxazoline-3-caboxylate, ethyl 5-(4-fiuoophenyl)-5-phenyl-2-isoxazoline- 3-caboxylate (cf. also elated compounds in WO-A-9i/0g202), 13-dimethylbut-l-yl 5-chloouinoline-g-oxyacetate, 4-allyloxybutyl 5-chloouinoline-g-oxyacetate, l-allyloxypop-2-yl 5-chloouinoline-g-oxyacetate, methyl 5-chloouinoxaline-g-oxyacetate, ethyl 5-chloouinoline-g-oxyacetate, allyl 5-chloouinoxaline-g-oxyacetate, 2-oxopop-l-yi 5-chloouinoline-g-oxyacetate, diethyl 5-chloouinoline-g-oxymalonate, diallyl 5-chloouinoxaline-g-oxymalonate, diethyl 5-chloouinoline-g-oxymalonate (cf. also elated compounds in EP-A-5g2i9g), 4-caboxychoman-4-ylacetic aC1d (AC-3044i5, cf. EP-A-6i36ig), 4-chloophenoxyacetic aC1d, 3,3'-dimethyl-4-methoxybenzophenone, l-bomo-4-chioomethyisulfonylbenzene, l-[4-(N-2-methoxybenzoylsulfamoyl)phenyli-3- methyluea (also known as N-(2-methoxybenzoyl)-4-[(methylaminocabonyl)- aminoibenzenesulfonamide), l-[4-(N-2-methoxybenzoyisulfamoyl)phenyli-3,3-dimethyluea, l-[4-(N-4,5-dimethylbenzoylsulfamoyl)phenyli-3-methyluea, l-[4-(N-naphthylsuifamoyl)phenyli-3,3-dimethyluea, N-(2-methoxy-5-methylbenzoyl)-4- (cyclopopylaminocabonyl)benzenesulfonamide, and/o one of the following compounds, defined by geneal fomulae, of the geneal fomula (i la) (Figue Removed) m epesents a numbe 0, 1 2, 3, 4 o 5, Ai epesents one of the divalent heteocyclic goupings shown below n epesents a numbe 0, 1 2, 3, 4 o 5, A2 epesents optionally CC4-alkyi- and/o C1-C4-alkoxy-cabonyl- and/o CpC4- alkenyloxy-cabonyl-substituted alkanediyl having i o 2 cabon atoms, 14 epesents hydoxyl, mecapto, amino, CpCe-alkoxy, C1-Ce-alkylthio, -Cealkylamino o di(C|-C4-aikyl)-amino, i5 epesents hydoxyl, mecapto, amino, CC7-alkoxy, CC6-alkenyloxy, C\-C&- alkenyloxy-C|-Cfi-alkoxy, CC6-alkylthio, C|-C6-alkylamino o di(C1-C4-alkyl)- amino, i6 epesents in each case optionally fluoine-, chloine- and/o bomine-substituted C C4-alkyl, epesents hydogen, in each case optionally fluoine-, chloine- and/o bominesubstituted C,-C6-alkyl, C2-C6-alkenyl o C2-C6-alkynyl, C1-C4-alkoxy-C,-C4-alkyl, dioxolanyl-CC4-alkyl, fuyl, fuyl-C1-C4-alkyl, thienyl, thiazolyl, pipeidinyl, o optionally fluoine-, chloine- and/o bomine- o C1-C4-aikyl-substituted phenyl, epesents hydogen, in each case optionally fluoine-, chloine- and/o bominesubstituted C|-C()-alkyl, C2-C6-alkenyl o C2-C6-alkynyl, C1-C4-alkoxy-CC4-alkyl, dioxolanyl-C|-Calkyl, fuyl, fuyl-CC4-alkyl, thienyl, thiazolyl, pipeidinyl, o optionally fluoine-, chloine- and/o bomine- o Cp-alkyl-substituted phenyl, i7 and ig also togethe epesent C3-C6-alkanediyl o C2-C5-oxaalkanediyl, each of which is optionally substituted by CC4-alkyl, phenyl, fuyl, a fused benzene ing o by two substituents which, togethe with the C atom to which they ae attached, fom a 5- o 6-membeed cabocycle, i9 epesents hydogen, cyano, halogen, o epesents in each case optionally fluoine-, chloine- and/o bomine-substituted C1-C4-alkyl, C3-C6-cycloalkyl o phenyl, 20 epesents hydogen, in each case optionally hydoxyl-, cyano-, halogen- o CC4- alkoxy-substituted CC6-aikyl, C3-C6-cycloalkyi oti-(CC4-alkyl)-siiyl, 2i epesents hydogen, cyano, halogen, o epesents in each case optionally fluoine-, chloine- and/o bomine-substituted C|-C4-alkyl, C3-C6-cycloalkyl o phenyl, Xi epesents nito, cyano, halogen, C|-C4-alkyl, CC4-haloalkyl, CC4-alkoxy o CC4-haloalkoxy, X2 epesents hydogen, cyano, nito, halogen, C,-C4-alkyl, C|-C4-haloalkyl, C1-C4- alkoxy o CChaloalkoxy, X3 epesents hydogen, cyano, nito, halogen, CC4-alkyl, C,-C4-haloalkyl, CC4- alkoxy o C|-C4-haloalkoxy, and/o the following compounds, defined by geneal fomulae, of the geneal fomula (lid) t epesents a numbe 0, 1 2, 3, 4 o 5, v epesents a numbe 0, 12,3,4 o 5, 22 epesents hydogen o CC4-alkyl, 23 epesents hydogen o CC4-alkyl, 24 epesents hydogen, in each case optionally cyano-, halogen- o CpC4-alkoxysubstituted CC6-alkyl, CC6-alkoxy, CC6-alkyithio, C1-C6-alkylamino o di(C,-C4- alkyl)-amino, o in each case optionally cyano-, halogen- o C1-C4-alkyl-substituted C3-C6-cycloalkyl, gC6-cycloaikyioxy, C3-C6-cycloaikylthio o C3-Cecycloalkylamino, 25 epesents hydogen, optionally cyano-, hydoxyl-, halogen- o C1-C4-alkoxysubstituted C|-C()-alkyl, in each case optionally cyano- o halogen-substituted C3-C6- alkenyl o C3-,-alkynyl, o optionally cyano-, halogen- o C|-C4-alkyl-substituted C2-Ce-cycloalkyl, 25 epesents hydogen, optionally cyano-, hydoxyl-, halogen- o CC4-alkoxysubstituted C1-C6-alkyl, in each case optionally cyano- o halogen-substituted C3-C6- alkenyl o C3-C6-aikynyl, optionally cyano-, halogen- o C1-C4-alkyl-substituted C3-C6-cycloalkyl, o optionally nito-, cyano-, halogen-, CC4-alkyl-, CC4-haloalkyl-, C1-C4-aikoxy- o CC4-haloalkoxy-substituted phenyl, o togethe with 25 epesents in each case optionally C|-C4-alkyl-substituted C2-C6-alkanediyl o C2-C$- oxaalkanediyl, X4 epesents nito, cyano, caboxyl, cabamoyl, fomyl, sulfamoyl, hydoxyl, amino, halogen, C|-C4-alkyl, CC4-haloalkyl, C,-C4-alkoxy o C1-C4-haioalkoxy, and X5 epesents nito, cyano. caboxyl, cabamoyl, fomyl, sulfamoyl, hydoxyl, amino, halogen, CC4-alkyl, CC4-haloalkyl, CC4-alkoxy o d-C4-haloalkoxy. i3. The composition as claimed in claim i2 in which the cop plant compatibility-impoving compound is selected fom the following goup of compounds: clouintocet-mexyl, fenchloazole-ethyl, isoxadifen-ethyl, mefenpy-diethyl, fuilazole, fencloim, cumyluon, dymon o the compounds iie-5 o iie-ii. 14. The composition as claimed in claim i2 in which the cop plant compatibility-impoving(Figue Removed) compound is mefenpy-diethyl. i5. A method fo contolling unwanted vegetation which compises allowing a composition as claimed in claim i2 to act on the plants o thei habitats. i6. The use of a composition as claimed in claim i2 fo contolling unwanted vegetation. i7. A method fo contolling unwanted vegetation which compises allowing a compound of the fomula (1) as claimed in claim i and a cop plant compatibility-impoving compound as claimed in claim i2 to act, sepaately in close tempoal succession, o as a mixtue, on the plants o thei habitats. |
---|
2012-delnp-2007-Correspondence Others-(11-02-2013).pdf
2012-delnp-2007-Correspondence Others-(21-01-2014).pdf
2012-DELNP-2007-Correspondence Others-(29-08-2011).pdf
2012-delnp-2007-Correspondence Others-(30-08-2012).pdf
2012-delnp-2007-Correspondence-Others-(08-07-2013).pdf
2012-delnp-2007-Correspondence-Others-(23-05-2013).pdf
2012-delnp-2007-Form-3-(08-07-2013).pdf
2012-delnp-2007-Form-3-(11-02-2013).pdf
2012-delnp-2007-Form-3-(21-01-2014).pdf
2012-DELNP-2007-Form-3-(29-08-2011).pdf
2012-delnp-2007-Form-3-(30-08-2012).pdf
2012-delnp-2007-Petition-137-(23-05-2013).pdf
2021-delnp-2007-correspondence-others.pdf
2021-delnp-2007-description(complete).pdf
Patent Number | 258885 | |||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Indian Patent Application Number | 2012/DELNP/2007 | |||||||||||||||||||||||||||||||||||||||||||||
PG Journal Number | 07/2014 | |||||||||||||||||||||||||||||||||||||||||||||
Publication Date | 14-Feb-2014 | |||||||||||||||||||||||||||||||||||||||||||||
Grant Date | 12-Feb-2014 | |||||||||||||||||||||||||||||||||||||||||||||
Date of Filing | 15-Mar-2007 | |||||||||||||||||||||||||||||||||||||||||||||
Name of Patentee | BAYER CROPSCIENCE AG | |||||||||||||||||||||||||||||||||||||||||||||
Applicant Address | ALFRED-NOBEL-STR.50, 40789 MONHEIM, GERMANY | |||||||||||||||||||||||||||||||||||||||||||||
Inventors:
|
||||||||||||||||||||||||||||||||||||||||||||||
PCT International Classification Number | C07D 207/36 | |||||||||||||||||||||||||||||||||||||||||||||
PCT International Application Number | PCT/EP2005/009807 | |||||||||||||||||||||||||||||||||||||||||||||
PCT International Filing date | 2005-09-13 | |||||||||||||||||||||||||||||||||||||||||||||
PCT Conventions:
|