Title of Invention	A PYRIDINE KETONE COMPOUND AND A COMPOSITION COMPRISING THE SAME
Abstract	ABSTRACT IN/PCT/2001/00339/CHE "Novel pyridine ketone and a composition comprising the same" This invention relates to compounds of formula I in which the substituents are as herein described are suitable for use as herbicides.

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PYRIDINE KETONES USEFUL AS HERBICIDES Novel herbicides-Trie present invention relates to novel herbicidally active pyridine ketones, to processes for their preparation, to compositions which comprise these compounds, and to their use for controlling weeds, in particular in crops of useful plants, or for inhibiting plant growth. Pyridine ketones having herbicidal action are described, for example, in WO 97/46530. We have now found novel pyridine ketones having herbicidal and growth-inhibiting properties. The present invention thus provides compounds of the formula I in which each R independently is CrC6alkyl, C2-C6alkenyl, C2-C6haloalkenyl, C2-C6alkynyl, C2-C6 haloalkynyl, C3-C6cycloalkyl, CrC6alkoxy, d-C6haloalkoxy, d-Cealkylttuo, d-C&aikylsuJfinyl, CrC6alkylsulfonyl, d-dhaloalkyl, d-Cehaloalkylthio, C,-C6haloalkylsulfinyl, C1-C6haloalkylsulfonyl, d-dalkoxycarbonyl, C1-C6alkylcarbonyl, C1-C6alkylamino, di-C1-C6 alkyiamino, C1-C6alkylaminosulfonyl, di-C1-C6alkylaminosulfonyl, -N(Ri)-S-R2) -N(R3)-SO-R4, -N(R5)-S02-R6, nitro, cyano, halogen, hydroxyl, amino, formyl, hydroxy-d-C6alkyl, C1-C6 alkoxy-d-Cealkyl, d-C6alkoxycarbonyloxy-d-dalkyl> C1-C6alkylthio-C1-C6alkyl, d-d alkylsulfinyl-d-C6aikyl, d-d>alkylsulfonyl-d-dalkyl, thiocyanato-d-C6alkyl, cyano-CrC6 alkyl, oxiranyl, C3-C6alkenyloxy, C3-C6alkynyloxy, d-C6alkoxy-C1-C6alkoxy, cyano-d-C6 alkenyloxy, d-C6alkoxycarbonyloxy-C1-C6alkoxy, C3-C6alkynyloxy, cyano-CrC6alkoxy, d-C6 alkoxycarbonyl-C1-C6alkoxy, d-C6alkylthio-d-C6alkoxy, alkoxycarbonyl-d-C6alkylthio, alkoxycarbonyl-d-C6alkylsulfinyl, alkoxycarbonyl-C1-C6alkylsulfonyl, d-C6alkylsulfonyloxy, C1-C6haloalkylsulfonyloxy, phenyl, benzyl, phenoxy, phenylthio, phenylsulfinyl,. phenylsulfonyl, benzylthio, benzylsulfinyl or benzylsulfonyl, where the phenyl groups may be mono- or polysubstituted by halogen, methyl, ethyl, trifluoromethyl, methoxy or nitro, or R is a five- to ten-membered monocyclic or fused bicyclic ring system, which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, where the ring system is either attached directly to the pyridine ring or attached to the pyridine ring via a C1-C4alkylene group, and where each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and where the ring system for its part may be mono-, di- or trisubstituted by d-C6alkyl, d-Cehaloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, d-C6alkoxy, d-dhaloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, C1-C6alkylthio, d-C6haloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, d-C6alkylsulfinyl, d-C6haloalkylsulfinyl, d-C6alkylsulfonyl, d-C6haloalkylsulfonyl, aminosulfonyl, d-C2alkylaminosulfonyi, C2-ddialkylaminosulfonyl, d-C3alkylene-R7, NR8R9, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by d-C3alkyl, C,-C3haloalkyl, C1-C3alkoxy, d-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; m is 1, 2, 3 or 4; p is 0 or 1 ; Ri, R3 and R5 independently of one another are hydrogen or d-C6alkyl; R2 is NR10Rn, d-C6alkoxy, d-C6haloalkoxy, d-C6alkyl, d-C6haloalkyl, C3-C6alkenyl, C3-C6 haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C3-C6cycloalkyl or phenyl, where phenyl for its part may be substituted by d-C3alkyl, d-C3haloalkyl, d-C3alkoxy, d-C3haloalkoxy, halogen, cyano or nitro; R4 is NRi2R13, d-C6alkoxy, d-C6haloalkoxy, d-C6alkyl, d-C6haloalkyl, C3-C6alkenyl, C3-C6 haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C3-C6cycloalkyl or phenyl, where phenyl for its part may be substituted by d-dalkyl, d-C3haloalkyl, d-C3alkoxy, CrC3haloalkoxy, halogen, cyano or nitro; R6is NR14Ri5, d-C6alkoxy, C1-C6haloalkoxy, d-C6alkyl, CrC6haloalkyl, C3-C6alkenyl, C3-C6 haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C3-C6cycloalkyl or pf\enyl, where phenyl for its part may be substituted by d-dalkyl, d-C3haloalkyl, d-C3alkoxy, d-C3haioalkoxy, halogen, cyano or nitro; R7 is C1-C3alkoxy, C2-C4alkoxycarbonyl, d-C3alkylthio, C1-C3alkylsulfinyl, CrC3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by d-Qjalkyl, C.i.-C3haloalkyl, CrC3 alkoxy, d-dhaloalkoxy, halogen, cyano or nitro;- Rs, R10, R12 and R14 independently of one another are hydrogen or CrC6alkyl; Rg, R11, R13 and R15 independently of one another are C1-C6alkyl or d-C6alkoxy; Q is the group Qi in which R16. R17, Ris and R19 independently of one another are hydrogen, hydroxyl, d-dalkyl, C2-C6 alkenyl, C2-C6alkynyl, d-dalkoxycarbonyl, CrC6alkylthio, C1-C6alkylsulfinyl, C1-C6 alkylsulfonyl, C1-C4alkyl-NHS(0)2, d-dhaloalkyl, -NH-d-dalkyl, -N(C1-dalkyl)2, d-C6 alkoxy, cyano, nitro, halogen or phenyl, which for its part may be substituted by d-dalkyl, d-dhaloalkyl, d-dalkoxy, C1-C4haloalkoxy, d-dalkylcarbonyl, d-dalkoxycarbonyl, amino, d-dalkylamino, di-d-dalkylamino, d-C6alkylthio, d-C6alkylsulfinyl, d-C6 alkylsulfonyl, d-dalkyl-S(0)20, d-dhaloalkylthio, d-dhaloalkylsulfinyl, d-d haloalkylsulfonyl, d-C4haloalkyl-S(0)20, d-dalkyl-S(0)2NH, C1-dalkyl-S(0)2N(C1-d alkyl), halogen, nitro, COOH or cyano; or two adjacent substituents from the group consisting of R16, R17, Ris and R19 form a C2-G6alkylene bridge; R20 is hydroxyl, 0'M\ halogen, cyano, SCN, OCN, d-d2alkoxy, Crdalkoxycarbonyl-d-d alkoxy, d-d2a!kylthio, CrC4alkylsulfinyl, d-d2alkylsulfonyl, d-C12haloalkylthio, d-d2 haloalkylsulfinyl, d-C12haloalkylsulfonyl, d-C6alkoxy-d-C6alkylthio, C1-C6alkoxy-C1-C6 alkylsulfinyl, d-C6alkoxy-d-C6alkylsulfonyl, d-d2alkenylthio, C2-C12alkenylsulfinyl, C2-d2 alkenylsulfonyl, d-d2alkynylthio, C2-C12alkynylsulfinyl, C2-C12alkynylsulfonyl, C2-C12 9 haloalkenylthio, d-C12haloalkenylsulfinyl, C2-C12haloalkenylsulfonyl, d-dalkoxycarbonyl- C1-C4alkylthio, d-dalkoxycarbonyl-d-dalkylsulfinyl, d-dalkoxycarbonyl-C1- dalkylsulfonyl, (d-dalkoxy)2P(0)0, d-dalkyl-(d-dalkoxy)P(9)0, H(d- dalkoxy)P(0)0, R37R38N, R71R72NNH-, R21R22NC(0)0-, R73R74NC(0)NH-, d-dalkyl-S(0)2NR39, d-d haloalkyl-S(O)2NR40, C1-dalkyl-S(0)20, d-dhaloalkyl-S(0)20, d-C18alkylcarbbnyloxy, where the alkyl group may be substituted by halogen, d-C6alkoxy, d.C6alkylthio or cyano, C2-C18alkenylcarbonyloxy, CrC1salkynylcarbonyloxy, C3-C6cycloalkylcarbonyloxy, CrC12 alkoxycarbonyloxy, C,-C12alkylthiocarbonyloxy, C1-C12alkylthiocarbamoyl, d-C6alkyl-NH(CS)N(CrC6alkyl)-NH-, di-d-C6alkyl-N(CS)N(d-C6aikyl)-NH-, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by C1-C4alkyl, d-dhaloalkyl, C1-C4alkoxy, CrC4haloalkoxy, C1-C4alkylcarbonyl, CrC4alkoxycarbonyl, C1-C4alkylamino, di-d-dalky!amino, d4alkylthio, CrC4alkylsulfinyl, d-C4alkylsulfonyl, d-C4alkyl-S(0)20, d-dhaloalkylthio, d-dhaloalkylsulfinyl, C1-C4 haloalkyisulfonyl, d-dhaloalkyl-S(0)20, d-C4alkyl-S(0)2NH, d-dalkyl-S(0)2N(d-d alkyl), halogen, nitro or cyano, or a group AMhio, Ar2-sulfinyl, Ar3-sulfonyl, -OCO-Ar4 or NH-Ar5 in which Ar1( Ar2, Ar3, Ar4 and Ar5 independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by d-C6alkyl, d-Cehaloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, d-C6alkoxy, d-dhaloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, d-C6alkylthio, d-C6haloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5 alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonyialkylthio, C2-dcyanoalkylthio, d-C6alkylsulfinyl, d-C6haloalkylsulfinyl, d-C6alkylsulfonyl, d-C6haloalkylsulfonyl, aminosulfonyl, d-dalkylaminosuifonyl, C2-C4dialkylaminosulfonyl, CrC3alkylene-R41, NR42R43, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by d-C3alkyl, d-C3haloalkyl, d-C3alkoxy, d-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; R4i is d-dalkoxy, d-dalkoxycarbonyl, d-C3alkylthio, d-C3alkylsulfinyl, C1-C3 alkylsulfonyl or phenyl, where phenyl for its part may be substituted by d-C3alkyl, d-C3 haloalkyl, d-C3alkoxy, d-C3haloalkoxy, halogen, cyano or nitro; R42 is hydrogen or d-C6alkyl; R43 is C1-C6alkyl or d-C6alkoxy; R21, R37, R39, Rio, R71 and R73 independently of one another are hydrogen or d-dalkyi; R22, R38, R72 and R74 independently of one another are hydrogen, d-C12alkyl, hydroxyl, d-d2alkoxy, C3-C6alkenyloxy or C3-C6alkynyloxy; or R21 and R22 together or R37 and R38 together or R71 and R72 together or R73 and R74 together are pyrrolidine piperidino, morpholino, thiornorpholino, which may be mono- or polysubstituted by methyl groups; , or are the group Q2 in which Y is a chemical bond, an alkylene group A,, carbonyl, oxygen, sulfur, sulfinyl, sulfonyl, -NHR248orNH(CO)R249; hi is C(R246R247)m0i ; A is C(R244R245)|-; r and m0i independently of one another are 0, 1 or 2; R240 is hydrogen, methyl or d-C3alkoxycarbonyl; R241, R242, R243, R244, R245, R246 and R247 independently of one another are hydrogen, halogen or methyi, or R243 together with an adjacent group R245 or R247 is a chemical bond; R248and R24g independently of one another are hydrogen or C1-C4alkyl; R23 is hydroxyl, 0'M+, halogen, cyano, SCN, OCN, d-C12alkoxy, C1-C4alkoxycarbonyl-CrC4 alkoxy, C1-C12alkylthio, d-C12alkylsulfinyl, CrC12alkylsulfonyl, d-C12haloalkylthio, C1-C12 haloalkylsulfinyl, C1-C4haloalkylsulfonyl, d-C6alkoxy-d-d>alkylthio, CrC6alkoxy-C1-C6 alkylsulfinyl, CrC6alkoxy-C1-C6alkylsuifonyl, C2-C12alkenylthio, C2-C12alkenylsulfinyl, C2-C12 alkenylsulfonyl, C2-C12alkynylthio, C2-C12alkynylsulfinyl, C2-C12alkynylsulfonyl, C2-C12 haloalkenylthio, C2-C12haloalkenylsulfinyl, C2-C12haloalkenylsulfonyl, d-dalkoxycarbonyl- d-dalkylthio, d-dalkoxycarbonyl-d-dalkylsulfinyl, d-dalkoxycarbonyl-d- dalkylsulfonyl, (C1-C4alkoxy)2P(0)0, d-dalkyl-(d-dalkoxy)P(0)0, H(d- dalkoxy)P(0)0, R44R45N, R75R76NNH-, R46R47NC(0)0-, RT7R78NC(0)NH-, C1-dalkyl-S(0)2NR4a, d-d haloalkyl-S(0)2NR49, d-dalkyl-S(0)20, C1-C4haloalkyl-S(0)20, d-dealkylcarbonyloxy, where the alkyl group may be substituted by halogen, d-C6alkoxy, d-d>alkylthio or cyano, C2-d8alkenylcarbonyloxy, C2-C18alkynylcarbonyloxy, C3-C6cycloalkylcarbonyloxy, d-d2 alkoxycarbonyloxy, d-C4alkylthiocarbonyloxy, C1-C12alkylthiocarbamoyl, d-C6alkyl- NH(CS)N(d-C6alkyl)-NH-, di-C1-C6alkyl-N(CS)N(C1-C6alkyl)-NH-, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by CrC4alkyl, C1-C4haloalkyl, d-dalkoxy, C1-C4haloalkoxy, d-dalkyicarbonyl, d-C4alkoxycarbonyl, C1-C4alkylamino, di-C1-C4alkylamino, d-dalkylthio, C1-C4alkylsulfihyl, d-C4alkylsulfonyl, C1-C4alkyl-S(0)20, C1-C4haloalkylthio, d-dhaloalkylsulfinyl, d-d haloalkylsulfonyl, C1-C4haloalkyl-S(0)20, d-dalkyl-S(0)2NH, C1-C4alkyl-S(0)2N(C1-C4 alkyl), halogen, nitro or cyano, or a group Ar6-thio, Ar7-sulfinyl, Ar8-sulfonyl, -OCO-Ar9 or NH-Ar10 in which Ar6, Ar7, Ar8, Ar9 and Ar10 independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by CrC6alkyl, CrC6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, d-C6alkoxy, d-dhaloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, C1-C6alkylthio, CrC6haloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5 alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, d-C6alkylsulfinyl, C1-C6haioalkylsulfinyl, C1-C6alkylsulfonyl, d-dhaloalkylsulfonyl, aminosulfonyl, d-Czalkylaminosulfonyl, C2-C4dialkylaminosulfonyl, CrC3alkylene-R5o, NR51R52, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by d-C3alkyl, d-C3haloaikyl, d-C3alkoxy, d-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; R50 is d-C3alkoxy, C2-dalkoxycarbonyl, C1-C3alkylthio, d-da'kylsulfinyl, C1-C3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, d-C3haloalkyl, d-d. alkoxy, d-C3haloalkoxy, halogen, cyano or nitro; R51 is hydrogen or d-C6alkyl; * R52 is C1-C6alkyl or d-C6alkoxy; R46, R4 , R4s, R49, R75 and R77 independently of one another are hydrogen or d-dalkyl; R47, R45, R76 and R78 independently of one another are hydrogen,d-d2alkyl, hydroxyl, d-C12alkoxy, C3-C6alkenyloxy or C3-C6alkynyioxy; or R4 and R45 together or R46 and R47 together or R75 and R76 together or R77 and R78 together are pyrrolidine piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups; or are the group Q3 in which R26 is hydroxyl, 0"M+, halogen, cyano, SCN, OCN, d-C4alkoxy, d-dalkoxycarbonyl-d-d alkoxy, CrC12alkylthio, d-d2alkylsulfinyl, C1-C12alkylsulfonyl, C1-C12haloalkylthio, C1-C12 haloalkylsulfinyl, d-d2haloalkylsulfonyl, d-dalkoxy-d-dalkylthio, d-C6alkoxy-d-C6 alkylsuifinyl, d-dalkoxy-d-C6alkylsulfonyl, C2-C12alkenylthio, C2-C12alkenytsulfinyl, C2-C12 alkenylsulfonyl, C2-C12alkynylthio, C2-C12alkynylsulfinyl, C2-d2alkynylsulfonyl, C2-C12 haloalkenylthio, C2-C12haloalkenylsulfinyl, C2-C12haloalkenylsulfonyl, d-dalkoxycarbonyl-d-dalkylthio, d-dalkoxycarbonyl-d-dalkylsulfinyl, d-dalkoxycarbonyl-d-dalkylsulfonyl, (d-C4alkoxy)2P(0)0, C1-C4alkyl-(C1-C4alkoxy)P(0)0, H(d-dalkoxy)P(0)0, R53R54N, R79R80NNH-, R55R56NC(0)0-, R8iR82NC(0)NH-, C1-C4alkyl-S(0)2NRS7, d-d haloalkyl-S(0)2NR58, d-dalkyl-S(0)20, C1-C4haloalkyl-S(0)20, d-d8alkylcarbonyioxy, where the alkyl group may be substituted by halogen, d-C6alkoxy, d.C6alkylthio or cyano, C2-C18aikenylcarbonyioxy, C2-C18alkynylcarbonyloxy, C3-C6cycloalkylcarbonyloxy, d-d2 alkoxycarbonyloxy, CrC12aikylthiocarbonyloxy, d-C12alkylthiocarbamoyl, C1-C6alkyl-NH(CS)N(d-C6alkyl)-NH-, di-d-C6alkyl-N(CS)N(C1-C6alkyl)-NH-, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by d-dalkyl, d-dhaloalkyl, d-dalkoxy, C1-dhaloalkoxy, d-dalkylcarbonyl, Crdalkoxycarbonyl, d-dalkylamino, di-C1-dalkylamino, d-dalkylthio, d-dalkylsulfinyl, d-dalkylsulfonyl, d-dalkyl-S(0)20, C,-dhaloalkylthio, d-dhaloalkylsulfinyl, d-d haloalkylsulfonyl, d-dhaloalkyl-S(0)20, d-dalkyl-S(0)2NH, C1-dalkyl-S(0)2N(d-d alkyl), halogen, nitro or cyano, or a group Arn-thio, Ar12-sulfinyl, Ar4-sulfonyl, -OCO-Ar14 or NH-A/15 in which Aru, Ar12, Ar13, Ar14 and Ar,5 independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be.mono-, di- or trisubstituted by d-dalkyl, C1-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, CrC6alkoxy, C1-C6haloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, C1-C6alkylthio, C,-C6haloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5 alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, d-C6alkylsulfinyl, CrC6haloalkylsulfinyl, C1-C6alkylsulfonyl, d-dhaloalkylsulfonyl, aminosulfonyl, C1-C2alkylaminosulfonyl, d-ddialkylaminosulfonyl, CrC3alkylene-R59, NReoRei, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by d-C3alkyl, CrC3haloalkyl, d-C3alkoxy, d-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; R59 is d-C3alkoxy, C2-C4alkoxycarbonyl, C1-C3alkylthio, C1-C3alkyisulfinyl, CrC3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, d-C3haloalkyl, d-d alkoxy, d-C3haloalkoxy, halogen, cyano or nitro; R6o is hydrogen or d-C6alkyl; R6i is d-C6alkyl or d-C6alkoxy; R55- R53 > R57- Rss, R79 and R8i independently of one another are hydrogen or d-dalkyl; R56, R54, Rso and R82 independently of one another are hydrogen, d-C12alkyl, hydroxyl, d-C12alkoxy, C3-C6alkenyloxy or C3-C6alkynyloxy; or R53 and R54 together or R55 and R56 together or R79 and Reo together or R81 and R82 together are pyrrolidine piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups; R29 is hydrogen, d-C6alkyl, d-dalkylcarbonyl, d-dalkoxycarbonyl, (d-dalkyl)NHCO, phenylaminocarbonyl, benzylaminocarbonyl or (d-C4alkyl)2NCO, where the phenyl and benzyl groups for their part may each be substituted by d-dalkyl, d-dhaloalkyl, d-d alkoxy, d-dhaloalkoxy, d-dalkylcarbonyl, d-dalkoxycarbonyl, d-dalkylamino, di-d-d alkylamino, d-dalkylthio, d-dalkylsulfinyl, d-dalkylsulfonyl, C1-dalkyl-S(0)20, d-d haloalkylthio, d-dhaloalkylsulfinyl, C1-C4haloalkylsulfonyl, C1-dhaloalkyl-S(0)20, d-d alkyl-S(0)2NH, d-dalkyl-S(0)2N(d-dalkyl), halogen, nitro or cyano; or is the group Q4 in which R30 is hydroxyl, O'W, halogen, cyano, SCN, OCN, C1-C12alkoxy, d-dalkoxycarbonyl-d-d alkoxy, CrC12alkylthio, CrC12alkylsuifinyl, CrC12alkylsulfonyl, C1-C12haloalkylthio, CrC12 haloalkylsulfinyl, C1-C12haloalkylsulfonyl, d-C6alkoxy-d-C6alkylthio, C1-C6alkoxy-C1-C6 alkylsulfinyl, d-dalkoxy-d-C6alkylsulfonyf, C2-C12alkenylthio, C2-C12alkenylsulfinyl, C2-C12 alkenylsulfonyl, C2-d2alkynylthio, C2-C12alkynylsulfinyl, C2-C12alkynylsulfonyl, C2-C12 haloalkenylthio, C2-C12haloalkenylsulfinyl, C2-C12haloalkenyisulfonyl, d-dalkoxycarbonyl-CrC4alkylthio, CrC4alkoxycarbonyl-C1-C4alkylsulfinyl, d-dalkoxycarbonyl-d-C4alkylsulfonyl, (d-C4alkoxy)2P(0)0, C1-C4alkyl-(C1-C4alkoxy)P(0)0, H(d-dalkoxy)P(0)0, ResResN, R83R8.NNH-, R64R65NC(0)0-, R85R86NC(0)NH-, d-dalkyl-S(0)2NR66, d-d haloalkyl-S(0)2NR67, C1-dalkyl-S(0)20, d-dhaloalkyl-S(0)20, CrC18alkylcarbonyloxy, where the alkyl group may be substituted by halogen, d-C6alkoxy, d-dalkylthio or cyano, C2-C18alkenylcarbonyloxy, C2-C18alkynylcarbonyloxy, C3-C6cycloalkylcarbonyioxy, d-d2 alkoxycarbonyloxy, d-C12alkylthiocarbonyloxy, C1-C12alkylthiocarbamoyl, d-C6alkyl-NH(CS)N(d-C6alkyl)-NH-, di-d-C6alkyl-N(CS)N(d-C6alkyl)-NH-, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by d-dalkyl, d-dhaloalkyl, d-dalkoxy, Crdhaloalkoxy, C1-dalkylcarbonyl, d-dalkoxycarbonyl, d-dalkylamino, di-d-dalkylamino, Crdalkylthio, C1-dalkylsulfinyl, Crdalkylsulfonyl, d-C4alkyl-S(0)20, d-dhaloalkylthio, d-dhaloalkylsulfinyl, d-d haloalkylsulfonyl, d-dhaloalkyl-S(0)20, d-C4alkyl-S(0)2NH, d-dalkyl-S(0)2N(d-d alkyl), halogen, nitro or cyano, or a group Ar16-thio, Ar17-sulfinyl, Ari8-sulfonyl, -OCO-Ar19 or NH-Ar20 in which Ar16, Ari7, Ar18, Ar19 and Ar20 independently of one another are a five- to ten-merribered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, ,and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by C1-C6alkyl, d-dhaloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, d-dalkoxy, d-dhaloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, d-dalkylthio, CrC6haloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5 alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, d-C6alkylsulfinyl, d-dhaloalkylsulfinyl, d-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, aminosulfonyl, C1-C2alkyiaminosulfonyl, C2-C4dialkylaminosulfonyl, CrC3alkylene-R68, NR69R70, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C1-C3alkyl, d-dhaloalkyl, CrC3alkoxy, d-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; R6B is d-dalkoxy, C2-C4alkoxycarbonyl, C1-C3alkylthio, d-dalkylsulfinyl, CrC3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by d-dalkyl, d-dhaloalkyl, d-d alkoxy, d-dhaloalkoxy, halogen, cyano or nitro; R70 is hydrogen or d-C6alkyl; R6, is d-dalkyl or d-C6alkoxy; R&4. Re2, Res, Re?, Ra3 and R85 independently of one another are hydrogen or d-dalkyl; Res, R63, RM and Rg6 independently of one another are hydrogen, d-d2alkyl, hydroxy!, d-C12alkoxy, C3-C6alkenyloxy or C3-C6alkynyloxy; or R62 and R63 together or RM and R65 together or R83 and R4 together or R85 and R86 together are pyrrolidine, piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups; R33 and R4 independently of one another are hydrogen, d-dalkyl, C2-C6alkenyl, C2-C6 alkynyl, d-C4alkoxycarbonyl, d-C6alkylthio, d-C6alkylsulfinyl, C1-C6alkylsulfonyl, C1-C4 alkyl-NHS(0)2, d-dhaloalkyl, -NH-d-dalkyl, -N(d-dalkyl)2, CrC6alkoxy or phenyl, which for its part may be substituted by d-dalkyl, d-dhaloalkyl, d-dalkoxy, d-dhaloalkoxy, d-dalkylcarbonyl, d-dalkoxycarbonyl, amino, d-C4a!kylamino, di-d-C4alkylamino, d-d alkylthio, d-C6alkylsulfinyl, d-dalkylsulfonyl, d-dalkyl-S(0)20, d-dhaloalkylthio, d-d haloalkylsulfinyl, d-dhaloalkylsulfonyl, d-dhaloalkyl-S(0)20, d-dalkyl-S(0)2NH, d-d alkyl-S(0)2N(d-dalkyl), halogen, nitro, COOH or cyano; or R33 and R4 together form a C2-C6alkylene bridge; and R35 is hydrogen, d-dalkyl, C3-C6alkenyl, C3-C6alkynyl or benzyl, which for its part may be substituted by halogen, methyl or methoxy, or is d-dalkoxycarbonyl or phenyl, which for its part may be substituted by d-dalkyl, d-dhaloalkyl, d-dalkoxy, d-dhaloalkoxy, d-d alkylcarbonyl, d-C4alkoxycarbonyl, amino, d-C4alkylamino, di-d-C4alkylamino, d-C4 alkylthio, C1-C4alkyisuifinyl, C1-C4alkylsulfonyl, d-C4alkyl-S(OkQ, d-dhaloalkylthio, d-d haloalkylsulfinyl,C1-C4haloalkylsulfonyl, C1-C4haloalkyl-S(0)20, d-C4alkyl-S(0)2NH, d-d alkyl-S(0)2N(C,-C4alkyl), halogen, nitro, COOH or cyano; or is the group Q5 in which Z is S, SO or S02; R01 is hydrogen, C1-C8alkyl, C1-C8alkyl substituted by halogen, d-C4alkoxy, d-C4alkylthio, C1-C4alkylsulfonyl, CrC4alkylsulfinyl, -CO2R02, -COR03, -COSR4, -NR05RO6, CONR036Ro37or phenyl, which for its part may be substituted by d-C4alkyl, CrC6haloaikyl, d-C4alkoxy, d-C4haloalkoxy, C2-C6alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, -COOH, COOd-C4alkyl, COOphenyl, d-dalkoxy, phenoxy, (C1-C4alkoxy)-d-d alkyl, (d-C4alkylthio)-d-C4alkyl, (C1-C4alkylsulfinyl)-d-dalkyl, (CrC4alkylsulfonyl)-d-C4 alkyl, NHS02-d-C4alkyl, NHS02-phenyl, N(CrC6alkyl)S02-d-C4alkyl, N(d-C6alkyl)S02-phenyl, N(C2-C6alkenyl)S02-C1-C4alkyl, N(C2-C6alkenyl)S02-phenyl, N(C3-C6alkynyl)S02-Cr dalkyl, N(C3-C6alkynyl)S02-phenyl, N(C3-C7cycloalkyl)S02-C1-C4alkyl, N(C3-C7 cycloalkyl)S02-phenyl, N(pJienyl)S02-CrC4alkyl, N(phenyl)S02-phenyl, OS02-d-C4alkyl, C0NR25R26, OS02-C,-C4haloalkyl, OS02-phenyl, d-C4alkyithio, d-C4haloalky!thio, phenylthio, C1-C4alkylsulfonyl, d-C4haloalkylsulfonyl, phenylsulfonyl, C1-C4alkylsulfinyl, d-dhaloalkylsulfinyl, phenylsulfinyl, d-C4alkyiene-phenyl or -NR0i5CO2R027; or R0i is C2-C8alkenyl or C2-C8alkenyl substituted by halogen, d-C4alkoxy, C1-dalkylthio, d-dalkylsulfonyl, C1-dalkylsulfinyl, -CONR032R033, cyano, nitro, -CHO, -CO2R03e, -COR039, -COS-C1-dalkyl, -NR034Ro35 or phenyl which for its part may be substituted by d-C4aikyl, C1-C6haloalkyl, d-C4alkoxy, CrC4haloalkoxy, C2-C6alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, -COOH, COOC1-C4alkyl, COOphenyl, C1-C4alkoxy, phenoxy, (d-C4alkoxy)-C,-C4alkyl, (C,-C4alkylthio)-C1-C4alkyl, {d-C4alkylsulfinyl)-d-C4aikyl, (d-C4alkylsulfonyl)-d-C4alkyl, NHS02-d-C4alkyl, NHS02-phenyl, N(C1-C6alkyl)S02-d-C4 alkyl, N(C1-C6alkyl)S02-phenyl, N(C2-C6alkenyl)S02-C1-C4alkyl, N(C2-C6alkenyl)S02-phenyl, N(C3-C6alkynyl)S02-d-C4alkyl, N(C3-C6alkynyl)S02-phenyl, N(C3-C7cycloalkyl)S02-d-C4 alkyl, N(C3-C7cycloalkyl)S02-phenyl, N(phenyl)S02-C1-C4alkyl, N(phenyl)S02-phenyl, 0S02-CrC4alkyl,.CONRo4oRo4i, OS02-d-C4haloaikyl, OS02-phenyl, d-C4alkylthio, C1-C4, haloalkylthio, phenyithio, CrC4alkylsuifonyl, CrC4haloalkylsulfonyl, phenylsulfonyl, C1-C4 alkylsulfinyl, CrC4haloalkylsulfinyl, phenylsulfinyl, CrC4alkylene-phenyl or -NR043CO2R042; or R0i is C3-C6alkynyl or C3-C6alkynyl substituted by halogen, CrC4haloalkyl, cyano, -CO2R044 or phenyl, which for its part may be substituted by d-C4alkyl, d-C6haloalkyl, d-C4 alkoxy, d-C4haloalkoxy, C2-C6alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, -COOH, COOd-C4alkyl, COOphenyl, d-dalkoxy, phenoxy, (d-C4 alkoxy)-d-C4alkyl, (C1-C4alkylthio)-CrC4alkyl, (d-dalkylsulfinyO-d-dalkyl, (d-d alkylsulfonyl)-d-dalkyl, NHS02-d-dalkyl, NHS02-phenyl, N(d-C6alkyl)S02-Crdalkyl, N(d-C6alkyl)S02-phenyl, N(C2-C6alkenyl)S02-d-C4alkyl, N(C2-C6alkenyl)S02-phenyl, N(C3-C6aikynyl)S02-d-C4alkyl, N(d-C6alkynyl)S02-phenyl, N(C3-C7cycloalkyl)S02-d-C4alkyl, N(C3-C7cycloalkyl)S02-phenyl, N(phenyl)S02-d-dalkyl, N(phenyl)S02-phenyl, 0S02-d-d alkyl, CONRo28Ro29, OS02-d-dhaloalkyl, OS02-phenyl, d-dalkylthio, d-dhaloalkylthio, phenyithio, d-dalkylsulfonyl, d-dhaloalkylsulfonyl, phenylsulfonyl, d-dalkylsulfinyl, d-dhaloaikylsulfinyl, phenylsulfinyl, d-dalkylene-phenyl or -NR03iC02Ro3o,' or R0i is drdcycloaikyl, C3-C7cycloalkyl substituted by C,-dalkyl, d-dalkoxy, d-d alkylthio, Crdalkylsulfinyl, C1-dalkylsulfonyl or phenyl, which for its part may be substituted by halogen, nitro, cyano, d-C4alkoxy, d-dhaloalkoxy, d-dalkylthio, d-dhaloalkylthio, C1-dalkyl and d-dhaloalkyl; or R01 is C1-dalkylene-C3-C7cycloalkyl, phenyl, or phenyl which is substituted by d-dalkyl, d-C6haloalkyl, CrC4alkoxy, d-dhaloalkoxy, C2-C6alkenyl, d-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, -COOH, COOd-C4alkyl, COOphenyl, d-dalkoxy, phenoxy, (d-dafkoxyj-d-dalkyl, (d-C4alkylthio)-d-C4alkyl, (d-dalkyisulfinyO-d-dalkyl, (CrC4alkylsulfonyl)-d-C4alkyl, NHS02-d-C4alkyl, NHS02-phenyl, N(CrC6alkyl)S02-d-C4 alkyl, N(d-C6alkyi)S02-phenyl, N(C2-C6alkenyl)S02-C1-C4alkyl, N(C2-C6alkenyl)S02-phenyl, N(C3-C6alkynyl)S02-C1-C4alkyll N(C3-C6alkynyl)S02-phenyl, N(C3-C7cycloaikyl)S02-d-C4 alkyl, N(C3-C7cycloalkyl)S02-phenyl, N(phenyl)S02-CrC4alkyl, N(phenyl)S02-phenyl, OS02-d-C4alkyl, CONRMSROAS, OS02-d-C4haloalkyl, OS02-phenyl, CrC4alkylthio, d-C4haloalkylthio, phenyithio, d-dalkylsulfonyl, d-dhaloalkylsuifonyl, phenylsulfonyl, CrC4 alkylsulfinyl, C1-C4haloalkylsulfinyl, phenylsulfinyl, or -NR048CO2RM?; or R01 is d-C4alkylene-phenyl, COR07 or 4-6-membered heterocyclyl; R02. Ro38. R044 and Roes independently of one another are hydrogen, C1-C4alkyl, phenyl, or phenyl which is substituted by C1-C4alkyl, C1-CehaloalkyI, d-dalkoxy, d-C4haloalkoxy, C2- C6alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, -COOH, COOCrC4alkyl, COOphenyl, d-dalkoxy, phenoxy, (C1-C4alkexy)-CrC4alkyl, (C1-C4 alkylthio)-C1-C4alkyi, (d-d'alkylsulfinyO-d-dalkyl, (C1-C4alkylsulfonyl)-C1-C4alkylf NHS02-d-C4alkyl, NHS02-phenyl, N(C1-C6alkyl)S02-C1-C4alkyl, N(C,-C6alkyl)S02-phenyl, N(C2-C6 alkenyl)S02-C1-C4alkyl, N(C2-C6alkenyl)S02-phenyl, N(C3-C6alkynyl)S02-C1-C4alkyt, N(C3-C6 alkynyl)S02-phenyl, N(C3-C7cycloalkyl)S02-d-C4alkyl, N(C3-C7cycloalkyl)SOrPhenyl, N(phenyl)S02-C1-C4alkyl, N(phenyl)S02-phenyf, OS02-C1-C4alkyl, CONR049R050. OS02-d-C4haloalkyl, OS02-phenyl, CrC4alkylthio, CrC4haloalkylthio, phenylthio, CrC4alkylsulfonyl, CrC4haioalkylsulfonyl, phenyisulfonyl, C1-C4alkylsulfinyl, CrC4haloalkylsulfinyl, phenylsulfinyl, C1-C4alkylene-phenyl or -NR052CO2R053; R03. R039 and Ro67 independently of one another are CrC4alkyl, phenyl or phenyl which is substituted by d-C4alkyl, d-C6haloalkyl, CrC4alkoxy, C1-C4haloalkoxy, C2-C6alkenyl, C3-C6 alkynyl, C3-C6alkenytoxy, C3-C6alkynyloxy, halogen, nitro, cyano, -COOH, COOC1-C4alkyl, COOphenyl, d-dalkoxy, phenoxy, (C1-C4alkoxy)-C1-C4alkyl, (CrC4alkylthio)-C1-C4alkyl, (CrC4alkylsurfinyl)-C1-C4alkyl, (d-dalkylsulfonyO-d-dalkyl, NHS02-C1-C4alkyl, NHS02-phenyl, N(C1-C6alkyl)S02-C1-C4alkyl, N(CrC6alkyl)S02-phenyl, N(C2-C6aikenyl)S02-C1-C4alkyl, N(C2-C6alkenyl)S02-phenyl, N(C3-C6alkynyl)S02-CrC4alkyl, N(C3-C6alkynyl)S02-phenyl, N(C3-C7cycloalkyl)S02-C1-C4alkyl, N(C3-C7cycloalkyl)S02-phenyl, N(phenyl)S02-Cr C4alkyl, N(phenyl)S02-phenyl, 0S02-C1-C4alkyl, CONR0070Ro54, OSOrC1-C4haloalkyl, OS02-phenyl, CrC4alkylthio, d-dhaloalkylthio, phenylthio, C1-C4alkylsulfonyl, d-C4haloalkylsulfonyl, phenyisulfonyl, d-C4alkylsulfinyl, d-C4haloalkylsulfinyl, phenylsulfinyl, d-C4alkylene-phenyl or -NR056CO2R055; R04 is C1-C4alkyl; R05 is hydrogen, d-C4alkyl, C2-C6alkenyl, C3-C6alkynyl, C3-C7cycloalkyl, phenyl or phenyl which is substituted by C1-C4alkyl, d-C6haloalkyl, d-dalkoxy, d-C4haloalkoxy, C2-C6 alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, -COOH, COOd-C4alkyl, COOphenyl, d-dalkoxy, phenoxy, (d-dalkoxyj-d-dalkyl, (d-C4 alkylthio)-d-C4alkyl, (d-C4alkylsulfinyl)-d-C4alkyl, (C1-C4alkylsulfonyl)-C1-C4alkyl, NHS02-d-C4alkyl, NHS02-phenyl, N(C1-C6alkyl)S02-C1-C4alkyl, N(d-C6alkyl)S02-phenyl, N(C2-C6 alkenyl)S02-C1-C4alkyl, N(C2-C6alkenyl)S02-phenyl, N(C3-C6alkynyl)S02H, N(C3-C6 alkynyl)S02-C,-C4alkyl, N(C3-C6alkynyl)S02-phenyl, N(C3-C7cycloalkyl)S02H, N(C3-C7 cycloalkyl)S02-C1-C4alkyll N(C3-C7cycloalkyl)S02-phenyl, N(phenyl)S02-d-C4alkyl, N(phenyl)S02-phenyl, OS02-d-C4alkyl, CONROSTROSS, OS02-d-C4haloalkyl, OS02-phenyl, d-C4alkylthio, C1-C4haloalkylthio, phenylthio, d-C4alkylsulfonyl, d-C4haloalkylsulfonyl, phenyisulfonyl, d-dalkylsulfinyl, C1-C4haloalkylsulfinyl, phenylsulfinyl, d-dalkylene- phenyl or -NR060CO2R059; Roe is hydrogen, d-dalkyl, C2-C6alkenyi, C3-C6alkynyl, C3-C7cycloalkyl, phenyl or phenyl which is substituted by C1-C4alkyl, d-dhaloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C2-C6 alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, -COOH, COOCrC4alkyl, COOphenyl, CrC4alkoxy, phenoxy, (C1-C4alkoxy)-CrC4alkyl, (d-d alkylthio)-C1-C4alkyl, (C,-C4alkylsulfinyl)-C1-C4alkyl, (C1-C4alkylsulfonyl)-C1-C4alkyl, NHS02- d-dalkyl, NHSOj-phenyl, N(d-dalkyl)S02-d-dalkyl, N(C,-C6alkyl)S02-phenyl, N(C2-C6 alkenyl)S02-C1-C4alkyl, N(C2-C6alkenyl)S02-phenyl, N(C3-C6alkynyl)S02-C1-C4alkyl, N(C3-C6 alkynyl)S02-phenyl, N(C3-C7cycloalkyl)S02-C1-C4alkyl, N(C3-C7cycioalkyl)S02-phenyl, N(phenyl)S02-CrC4alkyl, N(phenyl)S02-phenyl, 0S02-CrC4alkyl, CONR061R062, 0S02-Cr C4haloalkyl, OS02-phenyl, d-dalkylthio, d-dhaloalkylthio, phenylthio, d-C4alkylsulfonyl, d-dhaloalkylsulfonyl, phenyisulfonyl, d-dalkylsulfinyl, d-dhaloalkylsulfinyl, phenylsulfinyl, d-dalkylene-phenyl or -NRo64C02Ro63'> R07 is phenyl, substituted phenyl, d-dalkyl, d-dalkoxy or -NR0sRo9; Ros and R09 independently of one another are d-dalkyl, phenyl or phenyl which is substituted by halogen, nitro, cyano, d-dalkyl, d-dalkoxy, d-dthioalkyl, -C02Roe6. -COR067, Crdalkylsulfonyl, d-dalkylsulfinyl, d-dhaloalkyl; or R08 and R0g together form a 5-6-membered ring which may be interrupted by oxygen, NR065 or S, R015, R031, R043, Ro48> R052. Rose, Roeo and Ro64 independently of one another are hydrogen, d-dalkyl, C2-C6alkenyl, d-dalkynyl or C3-C7cycloalkyl; Ro25> Ro26, Ro27, Ro28. Ro29. Ro30> Ro32. Ro33. Ro34, Ro35. Ro36i Ro37, R()40i R()41, R(342. Ro45. Rw6» R047, R049, R0501 R053. ROM. Ross. R057, Rose. R059. R061. Ro62, R063. Roes and R070 independently of one another are hydrogen, d-dalkyl, C2-dalkenyl, d-dalkynyl, d-C7cycloalkyl, phenyl, or phenyl which is substituted by halogen, nitro, cyano, d-dalkoxy, d-dhaloalkoxy, d-dalkylthio, d-C4haloalkylthio, d-dalkyl or d-dhaloalkyl; and R36 is C1-C4alkyl, d-dhaloalkyi, C3-dalkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-d haloalkynyl, C3-dcycioalkyl or d-Cecycloalkyl which is substituted by halogen, d-dalkyl, d-dhaloalkyl, d-dalkenyl, C3-C6haloalkenyl, C3-dalkynyl, d-dhaloalkynyl, d-d alkoxycarbonyl, d-C4alkylthio, d-dalkylsulfinyl, d-dalkylsulfonyl, d-dhaloalkylthio, d-dhaloalkylsulfinyl, CrC4haloalkylsulfonyl, d-dalkylcarbonyl, di-C1-dalkyiamino, d-dalkoxy, C1-C4haloalkoxy, d-dalkyl-S(0)20, d-C4haloalkyl-S(0)20 or phenyl which for its part may be substituted by halogen, d-dalkyl, d-dhaloalkyl, d-C6alkenyl, C3-dalkynyl, cyano, nitro or COOH; and agronomically acceptable salts M+ and all stereoisomers and tautomers of the compounds of the formula I. , . - The compounds of the formula I can be present in different isomeric forms which can be isolated in pure form. The invention therefore also embraces all stereoisomeric forms of the compound of the formula I. Examples of these isomeric forms are the formulae Ix, Ixx, Ixxx and Ixxxx below, in which Q is the group Q2. The alkyl groups occurring in the definitions of the substituents can be straight-chain or branched and are, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, pentyl, hexyl, heptyl and octyl and their branched isomers. Alkoxy, alkenyl and alkynyl radicals are derived from the alkyl radicals mentioned. The alkenyl and alkynyl groups can be mono- or polyunsaturated. Halogen is generally fluorine, chlorine, bromine or iodine. This also applies, correspondingly, to halogen in combination with other meanings, such as haloalkyl or halophenyl. Haloalkyl groups preferably have a chain length of from 1 to 8 carbon atoms. Haloalkyl is, for example, fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2-fluoroethyl, 2-chloroethyl, pentafluoroethyl, 1,1-difluoro-2,2,2-trichloroethyl, 2,2,3,3-tetrafluoroethyl and 2,2,2-trichloroethyl; preferably trichloromethyl, difluorochloromethyl, difluoromethyi, trifluoromethyl and dichlorofluoromethyl. Suitable haloalkenyl groups are alkenyl groups which are mono- or polysubstituted by halogen, halogen being fluorine, chlorine, bromine and iodine and in particular fluorine and chlorine, for example 2,2-difluoro-1-methylvinyl, 3-fluoropropenyl, 3-chioropropenyl, 3-bromopropenyl, 2,3,3-trifluoropropenyl, 2,3,3-trichloropropenyl and 4,4,4-trifiuorobut-2-en-1-yl. Among the C3-C2oalkenyl groups which are mono-, di- or trisubstituted by halogen, preference is given to those having a chain length of from 3 to 5 carbon atoms. Suitable haloalkynyl groups are, for example, alkynyl groups which are mono- or polysubstituted by halogen, halogen being bromine, iodine and in particular fluorine and chlorine, for example 3-fluoropropynyl, 3-chloropropynyl, 3-bromopropynyl, 3,3,3-trifluoropropynyl and 4,4,4-trifluorobut-2-yn-1-yi. Among the alkynyl groups which are mono-or polysubstituted by halogen, preference is given to those having a chain length of from 3 to 5 carbon atoms. Alkoxy groups preferably have a chain length of from 1 to 6 carbon atoms. Alkoxy is, for example, methoxy, ethoxy, propoxy, i-propoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy and also the isomeric pentyloxy and hexyloxy radicals; preferably methoxy and ethoxy. Alkylcarbonyl is preferably acetyl or propionyl. Alkoxycarbonyl is, for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl or tert-butoxycarbonyl; preferably methoxycarbonyl or ethoxycarbonyl. Haloalkoxy groups preferably have a chain length of from 1 to 8 carbon atoms. Haloalkoxy is, for example, fluoromethoxy, difiuoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2,2-difluoroethoxy and 2,2,2-trichloroethoxy; preferably difiuoromethoxy, 2-chloroethoxy and trifluoromethoxy. Alkylthio groups preferably have a chain length of from 1 to 8 carbon atoms. Alkylthio is, for example, methylthio, ethylthio, propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio or tert-butylthio, preferably methylthio and ethylthio. Alkyisulfinyl is, for example, methylsulfinyl, ethylsulfinyl, propylsulfinyl, isopropylsulfinyl, n-butylsulfinyl, isobutylsulfinyl, sec-butylsulfinyl, tert-butylsuifinyl; preferably methylsulfinyl and ethylsulfinyl. Alkyisulfonyl is, for example, methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutylsulfonyl, sec-butylsulfonyl or tert-butylsulfonyl; preferably methylsulfonyl or ethylsulfonyl. Alkoxyalkoxy groups preferably have a chain length of from 1 to 8 carbon atoms. Examples of alkoxyalkoxy groups are: methoxymethoxy, methoxyethoxy, methoxypropoxy, ethoxymethoxy, ethoxyethoxy, propoxymethoxy or butoxybutoxy. Alkylamino is, for example, methylamino, ethylamino, n-propylamino, isopropylamino or the isomeric butylamines. Dialkylamino is, for example, dimethylamino, methylethylamino, diethylamino, n-propylmethylamino, dibutylamino and diisopropylamino. Preference is given to alkylamino groups having a chain length of from 1 to 4 carbcn atoms. Alkoxyalkyl groups have a chain length of preferably from 1 to 6 carbon atoms. Alkoxyalkyl is, for example, methoxymethyl, methoxyethyl, ethoxymethyl, ethoxyethyl, n-propoxymethyl, n-propoxyethyl, isopropoxymethyl or isopropoxyethyl. Alkylthioalkyl groups preferably have from 1 to 8 carbon atoms. Alkylthioalkyl is, for example, methylthiomethyl, methylthioethyl, ethylthiomethyl, ethylthioethyl, n-propylthiomethyl, n-propylthioethyl, isopropylthiomethyl, iso-propylthioethyl, butylthiomethyl, butylthioethyl or butylthiobutyl. The cycloalkyl groups preferably have from 3 to 8 ring carbon atoms, for example cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl. Phenyl, also as part of a substituent as phenoxy, benzyl, benzyloxy, benzoyl, phenylthio, phenylalkyl, phenoxyalkyl, may be substituted. In this case, the substituents can be in ortho, meta and/or para position. The preferred substituent positions are the ortho and para positions to the ring attachment point. Heterocyclyl is to be understood as meaning ring systems which, in addition to carbon atoms, contain at least one heteroatom, such as nitrogen, oxygen and/or sulfur. They can be saturated or unsaturated. In the context of the present invention, heterocyclyl ring systems may also be substituted. Suitable substituents are, for example, d-C4alkyl, C1-C4haloalkyl, CrC4alkoxy, cyano, nitro, d4alkylsulfonyl, C1-C4alkylsulfinyl, CrC4alkylthio or C3-C6cycloalkyl. Heterocyclyl may be, for example, furyl, thiophenyl, pyrrolidyl, piperidinyl, morpholinyl, pyridyl, imidazolyl, tetrahydrofuryl, tetrahydropyranyl, dihydrofuryl, dihydropyranyl, isoxazolyl, oxazolyl, isothiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazoJyi, thiazolyl, pyrazolyl, 1,2,4-triazolyl, 1,2,3-triazolyl, tetrazolyl, pyrimidyl, pyrazinyl, sym. orunsym. triazinyl, imidazolidinyl, dioxanyl, oxetanyl, in particular 2-oxetanyl, or phthalimidyl. The invention also embraces the salts M+ which can be formed by the compounds of the formula I, in particular the compounds of the formula I in which R20, R23, R26 and R30 are hydroxyl, preferably with amines, alkali metal and alkaline earth metal bases or quaternary ammonium bases. Among the alkali metal and alkaline earth metal bases, the hydroxides of lithium, sodium, potassium, magnesium or calcium, in particular those of sodium or potassium, may be especially emphasized as salt formers. Examples of amines suitable for ammonium salt formation are both ammonia and primary, secondary and tertiary d-C18alkylamines, d-C4ydroxyalkylamines and C2-C4alkoxyalkylamines, for example methylamine, ethylamine, n-propylamine, isopropylamine, the four isomeric butylamines, n-amylamine, isoamylamine, hexylamine, heptylamine, octylamine, nonylamine, decylamine, pentadecylamine, hexadecylamine, heptadecylamine, octadecylamine, methyiethylamine, methylisopropylamine, methylhexylamine, methylnonyfamine, methylpentadecylamine, methyloctadecyiamine, ethylbutylamine, ethylheptylamine, ethyloctylamine, hexylheptyl-amine, hexyloctylamine, dimethylamine, diethylamine, di-n-propylamine, diisopropylamine, di-n-butylamine, di-n-amylamine, diisoamylamine, dihexylamine, diheptylamine, dioctyl-amine, ethanolamine, n-propanolamine, isopropanolamine, N,N-diethanolamine, N-ethylpropanolamine, N-butylethanolamine, allylamine, n-butenyl-2-amine, n-pentenyl-2-amine, 2,3-dimethylbutenyl-2-amine, dibutenyl-2-amine, n-hexenyl-2-amine, propylene-diamine, trimethylamine, triethylamine, tri-n-propylamine, triisopropylamine, th-n-butylamine, triisobutylamine, tri-sec-butylamine, tri-n-amylamine, methoxyethylamine and ethoxyethylamine; heterocyclic amiines, for example pyridine, quinoline, isoquinoline, t morpholine, piperidine, pyrrolidine, indoline, quinuclidine and azepine; primary arylamines, for example anilines, methoxyanilines, ethoxyanilines, o,m,p-toluidines, phenylenediamines, naphthylamines and o,m,p-chloroanilines; but in particular triethylamine, isopropylamine and diisopropylamine. Quaternary ammonium bases which are suitable for salt formation are, for example, [N(Ra0i Rboi R coi Rdoi)]+ OH , where Raoi, Rboi. Red and Rdoi independently of one anotheer are CrC4alkyl. Further suitable tetraalkyiammonium bases with other anions can be obtained, for example, by anion exchange reactions. Preferred compounds of the formula I correspond to the formula lb . ,. . in which each R independently is d-C6alkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylthio, d-C6-alkylsulfinyl, CrC6alkylsuifonyl, d-C6haloalkyl, d-C6haloalkylthio, C1-C6haloalkylsulfinyl, d-C6haloalkylsulfonyl, d-C6alkoxycarbonyl, d-C6alkylcarbonyl, d-C6alkylamino, di-d-C6-alkylamino, d-C6alkylaminosulfonyl, di-d-'C6alkyiaminosulfonyl, -N(R1)-S-R2, -N(R3)-SO-R4, -N(R5)-S02-R6, nitro, cyano, halogen, hydroxy!, amino, or a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, where the ring system is either attached directly to the pyridine ring or attached via a d-dalkylene group to the pyridine ring, and each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and the ring system for its part may be mono-, di- or trisubstituted by d-C6aikyl, d-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, d-C6alkoxy, d-C6haloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, d-C6alkylthio, d-C6haloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4-cyanoalkylthio, d-C6alkylsulfinyl, d-C6haloalkylsulfinyl, d-C6alkylsulfonyl, d-C6-haloalkylsulfonyl, aminosulfonyl, C1-C2alkylaminosulfonyl, C2-ddialkylaminosulfonyl,.d-d-alkylene-R7, NR8Re, halogen, cyano, nitro, phenyl and benzylthio where phenyl and benzylthio for their part may be substituted on the phenyl ring by d-C3alkyl, d-C3haloalkyl, d-C3alkoxy, d-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; Q is the group Qi, in which R20 is hydroxyl, d-C4alkoxy, C1-C4aikylcarbonyloxy, d-dalkoxycarbonyloxy, R21R22N- C(0)0, phenylthio, d-dalkylthio, C1-C4alkyl-S(0)20, (CrC4alkoxy)2P(0)0, d-dalkyl(d- C4alkoxy)P(0)0, H(C1-C4alkoxy)P(0)0 or benzoyloxy; and R21 and R22 independently of one another are hydrogen or CrC4alkyl; or the group Q2a in which R23 is hydroxyl, d-C4alkoxy, d-dalkylcarbonyloxy, d-C4alkoxycarbonyloxy, R24R25N-C(0)0, phenylthio, CrC4alkylthio, CrC4alkyl-S(0)20, (CrC4alkoxy)2P(0)0, d-d- alkyl(d-dalkoxy)P(0)0, H(d-dalkoxy)P(0)0 or benzoyloxy; and R24 and R25 independently of one another are hydrogen or d-dalkyl; and Y is oxygen, sulfur, a chemical bond or a d-dalkylene bridge; or the group Q3 in which R26 is hydroxyl, d-dalkoxy, d-dalkylcarbonyloxy, d-dalkoxycarbonyloxy, R27R28N-C(0)0, phenylthio, d-dalkylthio, C1-dalkyl-S(0)20, (d-dalkoxy)2P(0)0, d-d- alkyl(d-dalkoxy)P(0)0, H(d-dalkoxy)P(0)0 or benzoyloxy; and R27 and R28 independently of one another are hydrogen or d-dalkyl and R29 is hydrogen, d-C6alkyl, d-dalkylcarbonyl, d-dalkoxycarbonyl, (d-dalkyl)NHCO or (d-dalkyl)2NCO; or the group Q4 in which R30 is hydroxyl, CrC4aikoxy, C1-C4alkylcarbonyloxy, d-dalkoxycarbonyloxy, R3iR32N-C(0)0, phenylthio, d-dalkylthio, d-C4alkyl-S(0)20, (CrC4alkoxy)2P(0)0, d-d-alkyl(CrC4alkoxy)P(0)0, H(C1-C4alkoxy)P(0)0 or benzoyloxy; and R31 and R32 independently of one another are hydrogen or Crdalkyl; R33 and R34 independently of one another are hydrogen, d-C4alkyl, C2-C6alkenyl, C2-Caaikynyl, d-C4-alkoxycarbonyl, d-Cealkylthio, C1-C6alkylsulfinyl, CrC6alkylsulfonyl, d-C4alkyl-NHS(0)2, C1-C4haloalkyl, -NH-CrC4alkyl, -N(CrC4alkyl)2, d-C6alkoxy, or phenyl which for its part may be substituted by C1-C4alkyl, d-dhaloalkyl, d-dalkoxy, d-dhaloalkoxy, d-dalkylcarbonyl, Crdalkoxycarbonyl, amino, d-dalkylamino, di-d-dalkylamino, d-C6alkylthio, d-C6-alkylsulfinyl, d-dalkylsulfonyl, d-dalkyl-S(0)20, d-C4haloalkylthio, d-dhaloalkylsulfinyl, d-dhaloaikylsulfonyl, d-dhaloalkyl-S(0)20, d-dalkyl-S(0)2NH, d-dalkyl-S(0)2N(d-d-alkyl), halogen, nitro, COOH or cyano; or R33 and R34 together form a d-C6alkylene bridge; and R35 is hydrogen, C,-C4alkyl, CrC4alkoxycarbonyl or phenyl which for its part may be substituted by C1-C4alkyl, d4haloalkyl, C4alkoxy, C4haloalkoxy, d-CUalkylcarbonyl, d-C4alkoxycarbonyl, amino, CrC4alkylamino, di-d-C4alkyiamino, C1-dalkylthio, d-d-alkylsulfinyl, C1-dalkylsulfonyl, C4alkyl-SfO4O, d-C4haloalkylthio, C4haloalkylsulfinyl, d-C4haloalkylsulfonyl, d-C4haloalkyl-S(0)20, d-C4aikyl-S(0)2NH, d-C4alkyl-S(0)2N(d-C4-alkyl), halogen, nitro, COOH or cyano; or the group Q5, and also agronomically acceptable salts of these compounds, the other substituents being defined as under formula I in claim 1. Among the compounds of the formula lb, preference is furthermore given to those in which the group -C(0)-Q is located in the 3 position on the pyridine ring, or in which Q is Q2, R23 being, in particular, hydroxyl, Y being a methylene bridge and m being the number 2. Preference is further given to compounds of the formula lb in which R is d-C6alkyl or CrCehaloalkyl. Preferred compounds of the formula I are characterized in that the group -C(0)Q is in the ortho position to a group R. Preference is furthermore given to compounds of the formula I in which a group R is CrCehaloalkyl and in the ortho position to the pyridyl nitrogen. Of particular interest are furthermore compounds of the formula I in which the group -C(0)Q is in the 3 position to the pyridyl nitrogen. In the formula I, p is preferably the number 0. Also to be emphasized are compounds of the formula I in which m is 2 and R is d-C3alkyl, d-C3-haloalkyl, d-C2alkoxymethyl, C1-C2alkythiomethyl, hydroxymethyl, d-Cealkylcarbonyloxymethyl, benzoyloxymethyl, d4alkoxycarbonyloxymethyl, chlorine, cyano, d-C3alkoxy, C1-C3haloalkoxy, allyloxy, propargyloxy, d-C3alkylthio, C1-C3alkylsulfinyi, d-C3alkylsulfonyl, d-C3alkylsulfonyloxy, C1-C2alkylsulfinylmethyl ord-C2alkylsulfonylmethyl. A further group of preferred compounds of the formula I is formed by those compounds in which at least one group R is trifluoromethyl, difluorochloromethyl, pentafluoroethyl or heptafluoro-n-propyl. • Particularly noteworthy compounds of the formula I are those in which Q is a group Q, and R16, R18 and R19 are C1-C3alkyl and R17 is hydrogen, or Q is a group Q2 and Y is -CH2-, -CH2CH2- or oxygen, A is -CH2- and R240, R24i, R242 and R243 are each hydrogen, or Q is a group Q3 and R29 is C1.C4alkylcarbonyl, d-C4alkoxycarbonyl or C14alkylaminocarbonyl or di(d-C2-alkyl)aminocarbonyl, or Q is a group Q4 in which R33, R34 and R35 are d-C3alkyl. In these noteworthy compounds of the formula I, R20, R23, R26 and R30 independently of one another are halogen, thiocyanato, d-C12alkoxy, C1-C4alkoxycarbonyl-d-C2alkoxy, C1-C12- alkylthio, C1-C12alkylsulfinyl, C1-C12alkylsulfonyl, d-C12haloalkylthio, d-C12haloalkylsuifinyl, d-C4haloalkylsulfonyi, d-C4alkenylthio, C2-d2alkenylsulfinyl, d>-C12alkenylsulfonyl, C2-C12-haloalkenylthio, C2-d2haloalkenylsulfinyl, C2-C12haioalkenylsulfonyl, C2-C12alkynyithio, C2-C12alkynylsulfinyl, C2-d2alkynylsulfonyl, d-C4alkoxycarbonyl-d-cV alkylthio, d-C4-alkoxycarbonyl-d-C2alkylsulfinyl, d-C4alkoxycarbonyl-d-C2alkylsulfonyl, C1-C4alkyl-S(0)2NH, d-C4haloalkyl-S(0)2NH, C1-C4alkyl-S(0)20, d-dsalkylcarbonyloxy, C2-C18-alkenylcarbonyloxy, C3-C6cycloalkylcarbonyioxy, d-C12alkoxycarbonyloxy, C1-C12-alkylthiocarbonyloxy, d-d2alkylthiocarbamoyl, d-Cealkyl-NH4SJNCd-CealkylJ-NH-, di-d-C6alkyl-N(CS)N(C1-C6alkyl)-NH-, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenyisulfonyl, phenylsulfonyioxy or benzoyloxy, where the phenyl groups for their part may in each case be substituted by d-C4alkyl, d-d-haloalkyl, d-C4alkoxy, d-dhaloalkoxy, d-C4alkylcarbonyl, d-dalkoxycarbonyl, d-d-alkylamino, di-d-C4alkylamino, d-dalkylthio, d-C4alkylsulfinyl, C1-C4alkyisuifonyl, d-C4-alkyl-S(0)20, d-C4haloalkylthio, C1-C4haloalkylsulfinyl, C,-dhaloalkylsulfonyl, d-d-haloalkyl-S(0)20, d-dalkyl-S(0)2NH, d-dalkyl-S(0)2N(d-C4alkyl), halogen, nitro or cyano, or R20, R23, R2e and R30 independently of one another are thienylcarbonyloxy or furylcarbonyloxy which for their part may be substituted by methyl or halogen, or are pyridylcarbonyloxy which for its part may be substituted as stated in claim 1, or R20 is RSTRSSN, R7IR72NNH-, R21R22NC(0)0-or R73R74NC(0)NH-; or R23 is R4R4N, R75R76NNH-, R46R47NC(0)0- or R4BNC4NH-; or R26 is R53R54N, R79R80NNH-, R55R56NC(0)0- or R81R82NC(0)NH-; or R30 is R62R63N, R83R84NNH-, FfoResNCfOJO- or R85R86NC(0)NH-. Very particularly preferably, R20, R23l R26 or R30 are hydroxyl or 0~M+. A further preferred group is formed by those compounds of the formula I in which Q is a group Q5, R36 is d-dalkyl, d-C4haloalkyl or cyclopropyl and R0i is d-C6alkyl, CrC4-alkoxycarbonylmethyl, C3-C8alkenyl, is benzyl or phenyl substituted by methyl, halogen, trifluoromethyl, methoxy, and at least one group R is trifluoromethyl, difluorochloromethyl, pentafluoroethyl or heptafluoro-n-propyl located in the ortho position to the pyridyl nitrogen. t The process according to the invention for preparing compounds of the formula I is carried out analogously to known processes (for example those described in WO 97/46530 and EP-A-0 353 187) and comprises A) reacting a compound of the formula II t in which R and m are as defined under formula I and X is a leaving group, for example halogen, in an inert organic solvent in the presence of a base with compounds of the formula III, IV.V or VI in which R16, R17, Ri8, Rig,R29, R33, R34, R35, R240, R243, R242, R241, A and Y are as defined under formula I to give the compounds of the formula VII, VIII, IX or X and then isomerizing these compounds, for example in the presence of a base and a catalytic amount of dimethylaminopyridine (DMAP) or a source of cyanide; or b) reacting a compound of the formula XI in which R and m are as defined under formula I with compounds of the formula III, IV, V or VI in which Ri6, R17. R-is, R19, R29, R33. R34, R35, R240, R243, R242> R241, A and Y are as defined under formula I in an inert, organic solvent in the presence of a base and a coupling agent to give a compound of the formula VII, VIII, IX or X and then isomerizing these compounds, for example as described under route a). Compounds of the formula I in which R2o, R23, R26 and R30 are different from hydroxyl or halogen can be prepared by converesion methods which are generally known from the literature, for example acyclations or carbamoylations with appropriate acyl chlorides, from compounds in which R20, R23, R26 or R30is hydroxyl in the presence of a suitable base, or they can be prepared by nucleophilic substitution reactions on chlorides of the formula I in which R20, R23, R26 or R30 is halogen, which are likewise obtainable by known processes by reaction with a chlorinating agent, such as phosgene, thionyl chloride or oxalyl chloride. Here, for example, suitably substituted amines, or hydroxylamines directly, or alkylsulfonamides, mercaptans, thiophenols, phenols, ArrNH2 or ArySH, are employed in the presence of a base, for example 5-ethyl-2-methylpyridine, tiiisopropylethylamine, triethylamine, sodium bicarbonate, sodium acetate or potassium carbonate. Compounds of the formula I in which R20, R23, R26 or R30 comprise thio groups can be oxidized analogously to known standard processes, for example using peracids, for example meta-chloroperbenzoic acid (m-CPBA) or peracetic acid, to give the corresponding sulfones and sulfoxides of the formula I. Here, the degree of oxidation at the sulfur atom (SO- or S02-) can be controlled by the amount of oxidizing agent. The process according to the invention for preparing compounds of the formula I in which R and m are as defined under formula I and Q is a group in which Z is sulfur, q is 0 and R36 and R0i are as defined under formula I is carried out analogously to known processes (for example those described in WO 97/43270) and comprises converting a compound of the formula XII in which R36, R and m are as defined under formula I in the presence of a base, carbon disulfide and an alkylating agent of the formula XIII in which R0i is as defined under formula I and X, is a leaving group, for example halogen or sulfonate, into the compound of the formula XIV in which Z is sulfur and R, R0i, R36 and m are as defined above and then cyclizing this compound using hydroxylamine hydrochloride, in the presence or absence of a solvent, in the presence of a base to give the compounds of the formulae in which Z is sulfur and R, R36, R01 and m are as defined above, and then oxidizing these compounds with an oxidizing agent, for example meta-chloroperbenzoic acid (m-CPBA). The isomers of the formulae le and If can be separated using column chromatography and a suitable mobile phase and then purified. The preparation of the compounds of the formula I in which p is 0 is illustrated in more detail in the reaction schemes 1 and 2 below. According to this reaction scheme, the compounds of the formula I with the group Q, in which R20 is hydroxy I, the compounds of the formula I with the group Q2 in which R23 is hydroxyl, the compounds of the formula I with the group Q3 in which R26 is hydroxyl and the compounds of the formula I with the group Q4 in which R30 is hydroxy! can preferably be prepared. For preparing the compounds of the formula I in which Q is the groups Qi to Q4 and R20, » R23)R26 and R30 are hydroxyl, in accordance with reaction scheme 1, route a), the carboxylic acid derivatives of the formula II in which X is a leaving group, for example halogen, for example iodine, bromine and in particular chlorine, N-oxyphthalimide or N,0- dimethylhydroxylamino or part of an activated ester, for example (formed from dicyclohexylcarbodiimide (DCC) and the corresponding carboxylic acid) or C2H5N c NH(CH2)3N(CH3)2 (formed from N-ethyl-N'-(3-dimethylaminopropyl)carbodiimide (EDC) and the corresponding carboxylic acid) are employed. These compounds are reacted in an inert organic solvent, for example a halogenated hydrocarbon, for example dichloromethane, a nitrile, for example acetonitrile, or an aromatic hydrocarbon, for example toluene, and in the presence of a base, for example an alkylamine, for example triethylamine, an aromatic amine, for example pyridine or 4-dimethylaminopyridine (DMAP), with the dione derivatives of the formula III, IV, V or VI to give the isomeric enol ethers of the formulae VII, VIII, IX and X. This esterification is carried out at temperatures of from 0°C to 110°C. The isomerization of the ester derivatives of the formulae VII, VIII, IX and X to the dione derivatives of the formula I (in which R2o, R23. R26 and R30 are hydroxyl) can be carried out, for example, analogously to EP 369 803 in the presence of a base, for example an alkylamine, for example triethylamine, a carbonate, for example potassium carbonate, and a catalytic amount of DMAP or a cyanide source, for example acetone cyanohydrin or potassium cyanide. According to reaction scheme 1, route b), the desired diones of the formula I (in which R20, R23, R26 and R30 are hydroxyl) can be obtained, for example, in analogy to Chem. Lett. 1975, 1045 by esterifying the carboxylic acids of the formula XI with the dione derivatives of the formula III, IV, V or VI in an inert solvent, for example a halogenated hydrocarbon, for example dichloromethane, a nitrile, for example acetonitrile, or an aromatic hydrocarbon, for example toluene, in the presence of a base, for example an alkylamine, for example triethylamine, and a coupling agent, for example 2-chloro-1-methylpyridinium iodide. Depending on the solvent used, this esterification is carried out at temperatures of from 0°C to 110°C, affording initially, as described under route a), the isomeric ester of the formula I which can be isomerized as described under route a), for example in the presence of a base and a catalytic amount of DMAP, or a cyanide source, to give the desired dione derivative of the formula I (R20, R231 R26 and R30 are hydroxyl). '• The preparation of the compounds of the formula I in which Q is the group Q5 can be carried out in accordance with reaction scheme 2 by reacting the (3-diketone derivative of the formula XII, for example in analogy to Synthesis 1991, 301; ibid. 1988, 793; or Tetrahedron.32, 3055 (1976) with carbon disulfide in the presence of a base, for example a carbonate, for example potassium carbonate, a metal hydride, for example sodium hydride, or potassium fluoride on aluminium, and an alkylating agent of the formula XIII in which *Xi is a leaving group, for example halogen, for example iodine, bromine and in particular carried out in the presence of a solvent, for example an amide, for example N,N-dimethylformamide (DMF), a sulfoxide, for example dimethylsuifoxide (DMSO), or a nitrile, for example acetonitrile. The ketene thioacetal of the formula XIV which is formed is cyclized with the aid of hydroxylamine hydrochloride in the presence of a base, for example sodium acetate, in a solvent, for example an alcohol, for example ethanol, or an ether, for example tetrahydrofuran, to give the compound of the formula le in which Z is sulfur. This cyclization reaction is carried out at temperatures of from 0°C to 100°C. If appropriate, compounds of the formulae le and If (Z is sulfur) can be oxidized analogously to known standard processes, for example with peracids, for example meta-chloroperbenzoic acid (m-CPBA) or peracetic acid, to give the corresponding sulfones and sulfoxides of the formulae le and If (Z = SO- or S02-). Here, the degree of oxidation at the sulfur atom (Z = SO- or S02-) can be controlled by the amount of oxidizing agent. Oxidations to the compounds of the formulae le and If (Z is SO- or S02-) are carried out as described, for example, in H.O. House, "Modern Synthetic Reactions" W. A. Benjamin, Inc., Menlo Park, California, 1972, pages 334-335 and 353-354. The activated carboxylic acid derivatives of the formula II in reaction scheme 1 (route a) in which X is a leaving group, for example halogen, for example bromine, iodine or in particular chlorine, can be prepared by known standard processes, as described, for example, in C. Ferri "Reaktionen der organischen Synthese" [Reactions of Organic Synthesis], Georg Thieme Verlag, Stuttgart, 1978, page 461 ff. Tt)is is shown in reaction scheme 3 below. According to reaction scheme 3, the compounds of the formula II (X=leaving group) or II (X=halogen) are prepared, for example, by employing a halogenating agent, for example a thionyl halide, for example thionyl chloride or thionyl bromide; a phosphorus halide or phosphorus oxyhalide, for example phosphorus pentachloride or phosphorus oxychloride or phosphorus pentabromide or phosphoryl bromide; or an oxalyl halide, for example oxalyl chloride, or by employing a reagent for the formation of activated esters, for example N,N'-dicyclohexylcarbodiimide (DCC) or N-ethyl-N'-(3-dimethylaminopropyl)carbodiimide (EDC) of the formula X. For the compound of the formula X used as halogenating agents, X is a leaving group, for example halogen, for example fluorine, bromine or iodine and in particular chlorine, and W, is, for example, PCI2, SOCI, SOBr or CICOCO. The reaction is carried out in the presence or absence of an inert organic solvent, for example in aliphatic, halogenated aliphatic, aromatic or halogenated aromatic hydrocarbons, for example n-hexane, benzene, toluene, xylenes, dichloromethane, 1,2-dichloroethane or chlorobenzene, at reaction temperatures in the range of from -20°C to the reflux temperature of the reaction mixture, preferably at 40-150°C, and in the presence of a catalytic amount of N,N-dimethylformamide. Such reactions are generally known and described in the literature in various variations with respect to the leaving group X. The compounds of the formulae III, IV, V and VI are known and can be prepared analogously to the methods described, for example, in WO 92/07337, DE-A-3818958, EP-A-0 338 992 and DE-A-3902818. The compounds of the formula XII in reaction scheme 2 can be obtained by standard processes, for example from the corresponding compounds of the formula II in which R and m are as defined above and X is a leaving group, for example halogen, for example via Claisen condensation, or from the compounds of the formula II by reaction with a ketocarboxylic acid salt of the formula XV in which R36 is as defined under formula I and M+ is an alkali metal ion (cf., for example, WO 96/26192). The compounds of the formulae II and XI are known and can be prepared analogously to the methods described, for example, in WO 97/46530, EP-A-0 353 187, Heterocycles, 48, 779 (1998), Heterocycles, 46, 129 (1997), or Tetrahedron Letters, 1749 (1998). For preparing all other compounds of the formula I functionalized according to the definition of (R)m, there is a large number of known standard processes available, for example alkylation, halogenation, acylation, amidation, oximation, oxidation and reduction, and the choice of the suitable preparation processes depends on the properties (reactivities) of the substituents in the intermediates in question. All further compounds originating from the scope of the formula I can be prepared in a simple manner, taking into account the chemical properties of the pyridyl or Q moiety. The end products of the formula I can be isolated in a customary manner by concentration or evaporation of the solvent and be purified by recrystallization or trituration of the solid residue in solvents in which they are only sparingly soluble, such as ethers, aromatic hydrocarbons or chlorinated hydrocarbons, by distillation or by means of column chromatography and a suitable mobile phase. Furthermore, it is known to the person skilled in the art in which order certain reactions have to be carried out advantageously to avoid possible side reactions. Unless a targeted synthesis is carried out for isolating pure isomers, the product may be obtained as a mixture of two or more isomers. The isomers can be separated by methods known per se. Compounds of the formula I in which p is 1, i.e. the corresponding N-oxides of the formula I, can be prepared by reacting a compound of the formula I in which p is 0 with a suitable oxidizing agent, for example with the H202 urea adduct, in the presence of an acid anhydride, for example trifluoroacetic anhydride. This reaction sequence is demonstrated using the example of group Q2 below: Compounds of the formula I in which R in the ortho position to the pyridine nitrogen is 1-chloro-C1-C2alkyl, 1-hydroxy-C1-C2alkyl, 1-(C1-C6alkylcarbonyloxy)-CrC2alkyl, 1-benzoyloxy-d-C2alkyl, 1 -(CrC4alkoxycarbonyloxy)-C1-C2alkyl, 1 -(C1-C4alkylthio)-C1-C2alkyl, 1 -(Cl-C4-alkylsulfinyl)-C1-C2alkyl, 1 -(C1-C4alkylsulfonyl)-C1-C2alkyl, 1 -thiocyanato-C1-C2alkyl, 1-cyano-C1-C2alkyl, can also be prepared, for example, by heating an N-oxide of the formula I under known reaction conditions, for example in the presence of tosyl chloride (see, for example, Parham, W. £.; Sloan, K. B.; Reddy, K. R.; Olson, P. E.; J Org Chem 1973, 38, 927) or in the presence of an acid anhydride (see, for example, Konno, K.; Hashimoto, K.; Shirahama, H.; Matsumoto, T.; Heterocycles 1986, 24, 2169), followed, if appropriate, by subsequent conversion. The compounds of the formula XXIIa are synthesized analogously to known processes, for example those mentioned in Heterocycles, 46, 129 (1997) or Helvetica Chimica Acta 71, 596 (1988), and comprises either a) acylating a compound of the formula XVI in which R3m is hydrogen or C1-C6alkyl; R40i is hydrogen, CrC6alkyi ,C2-C6aikenyl, C3-C6cycloalkyl, CrC6alkoxy, C1-C6alkylthio, d-C6alkylsulfinyl, CrC6haloalkyl, 1-(d-C6alkylcarbonyloxy)-d-C6alkyl, 1-(d-C6alkylthio)-d-Ce-alkyl, 1 -{d-C6alkylsulfinyl)-d-C6alkyl, 1 -(d-C6alkylsulfonyl)-d-C6alkyl, 1 -thiocyanato-d-Ce-alkyl, 1-cyano-d-C6alkyl, phenyl, where the phenyl groups may be mono- or polysubstituted by halogen, methyl, ethyl, trifluoromethyl, methoxy or nitro, or is a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, where the ring system is either attached directly or via a d-dalkylene group to the double bond, and each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms and the ring system for its part may be mono-, di- or trisubstituted by d-C6alkyl, d-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3d6haloalkynyl, d-C6alkoxy, d-C6haloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, d-C6alkylthio, d-C6haloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-Csalkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, d-C6alkylsulfinyl, d-C6haloalkyisulfinyl, d-C6alkylsulfonyl, d-C6haloalkylsulfonyl, aminosulfonyl, d-C2alkylaminosulfonyl, C2-C4dialkyiaminosulfonyl, C1-C3alkylene-R87, NR88R89, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by d-C3alkyl, d-C3haloalkyl, d-C3alkoxy, d-C3-haloalkoxy, halogen, cyano or nitro and where substituents on nitrogen in the heterocyclic ring are different from halogen; R87 is d-C3alkoxy, C2-daikoxycarbonyl, d-C3alkylthio, d-C3alkylsulfinyl, d-dalkylsulfonyl or phenyl, where phenyl for its part may be substituted by d-C3alkyl, d-C3haloalkyl, d-C3-alkoxy, d-C3haloalkoxy, halogen, cyano or nitro; R88 is hydrogen or d-C6alkyl and R89 is d-C6alkyl or d-C6alkoxy; with a compound of the formula XVII in which R501 is C,-C6haioall in which R30i, R401, R501 and Ri4are as defined above, in the presence of a base, for example an aromatic amine, for example pyridine, and subsequently replacing the alkoxy group by the amino group using ammonia in an organic solvent, for example a halogenated hydrocarbon, for example dichloromethane, or a nitrile, for example acetonitrile. The resulting compound of the formula XIX is subsequently condensed with a compound of the formula XX in which R201 is d-C6alkyl, C2-C6alkenyl, C2-C6haloalkenyl, C2-C6alkynyl, C2-C6-haloalkynyl, C3-C6cycloalkyl, CrC6haloalkyl, 1-(Cl-C6alkylcarbonyloxy)-C1-C6alkyl, 1-(C1-C6alkylthio)-Cr C6alkyl, 1 -(d-dalkylsulfinyl)-d-C6alkyl, 1 -(d-dalkylsulfonyl)-d-C6alkyl, 1 -thiocyanato-C-C6alkyl, 1-cyano-CrC6alkyl, d-C6alkoxy-d-dalkyl, C1-C6alkoxycarbonyl-C-|-d5alkoxy, d-Cealkylthio-d-Cealkoxy, phenyl, benzyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, benzylthio, benzylsulfinyl or benzylsulfonyl, where the phenyl groups may be mono- or polysubstituted at least by halogen, methyl, ethyl, trifluoromethyl, methoxy or nitro, or is a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group'consisting of nitrogen, oxygen and sulfur, where the ring system is attached either directly or via a d- d-alkylene group and each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and the ring system for its part-may be mono-, di- or trisubstituted by C1-C6alky|, C1-C6haloalkyl, C3-C6alkenyl, C3-C6halbalkenyi, C3-C6alkynyl, C3.C6haloalkynyl, CrC6alkoxy, CrC6haioalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, CrC6alkylthio, d-Cehaloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, d-C6alkylsulfinyl, d-C6haioalkylsulfinyl, d C6alkylsulfonyl, d-C6haloalkylsulfonyl, aminosulfonyl, C1-C2alkylaminosulfonyl, C2-C4dialkylaminosulfonyl, d-C3-R90, NR91R92, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by CrC3alkyl, CrC3haloalkyl, d-C3alkoxy, d-C3-haloalkoxy, halogen, cyano or nitro, and where substituents on nitrogen in the heterocyclic ring are different from halogen; R90 is d-C3alkoxy, C2-dalkoxycarbonyl, d-C3alkylthio, d-C3alkylsulfinyl, d-C3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by d-C3-alkyl, d-C3haloalkyl, d-C3-alkoxy, d-C3haloalkoxy, halogen, cyano or nitro; R91 is hydrogen or d-C6alkyl and R92 is d-C6alkyl or CrC6alkoxy and RM is as defined above, and the resulting compound of the formula XXIa is subsequently hydrolysed to give the compound of the formula XXIIa in which R20i, R301, R401 and R50i are as defined above, or b) condensing a compound of the formula XXIII in which R30i, R401, R501 and R,4are as defined above (using, for example, POCI3), and subsequently reacting this compound with a nucleophile of the formula XXVII Z-R150 (XXVII) In which Z is SH, OH or amino and R150 is d-C6alkyl, C3-C6alkenyk, C3-C6halogenalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C1-C6alkylsulfonyl, CrC6haloalkyl, phenyl, benzyl, where the phenyl and benzyl groups for their part may be substituted by d-C3alkyl, CrC3haloalkyl, C1.C3alkoxy, CrC3haloalkoxy, halogen, cyano or nitro, is d-C4alkoxy-C1-C4alkyl or C,-C4-alkylthio-C1-C4alkyl, C1-C4alkylsulfinyl-C1-C4alkyl, CrC4alkylsulfonyl-C1-C4alkyl, or a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and the ring system for its part may be mono-, di- or trisubstituted by CrC6alkyl, d-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6-alkynyl, C3-C6haloalkynyl, d-C6alkoxy, d-Cehaloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, ... mercapto, d-C6alkylthio, C1-C6haloalkylthio, C3-C6alkenylthio, C3-C6hak>alkenylthio, C3-C6-alkynylthio, C2-C5alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4-cyanoalkylthio, d-C6alkylsulfinyl, d-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, d-C6-haloalkylsulfonyl, aminosulfonyl, C1-C2alkylaminosulfonyl, C2-ddialkylaminosulfonyl, d-C3-aikylene-R93, NR94R95, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by d-C3alkyl, d-C3-haloalkyl, d-C3alkoxy, d-C3haloalkoxy, halogen, cyano or nitro, and where substituents on nitrogen in the heterocyclic ring are different from halogen; R93 is d-C3alkoxy, C2-dalkoxycarbonyl, d-C3alkylthio, d-C3alkylsulfinyl, d-C3alky!sulfonyl or phenyl, where phenyl for its part may be substituted by CrC3alkyl, C1-C3haloalkyl, d-C3-alkoxy, C1-C3haioalkoxy, halogen, cyano or nitro; R94 is hydrogen or d-C6alkyl and R95is d-C6alkyl or d-C6alkoxy; Compounds of the formula XXIb in which R150 is fluorine are prepared by reacting a compound of the formula XXVI in the presence of a polar aprotic solvent, for example acetonitrile, dimethylformamide or sulfolane, with potassium fluoride in the presence or absence of a catalytic amount of 18-crown-6. Compounds of the formula XXIc in which R150 is hydrogen are preparerd by reducing the chlorine group in the formula XXVI, for example using hydrogen in the presence of a suitable metal catalyst or using ammonium formate in a suitable solvent. The preparation of the compounds of the formula XXIIa, or XXIIb and XXIIc is illustrated in more detail in the reaction schemes 4 and 5 below. For preparing all other compounds of the formula I which are functionalized according to the definition of R201 (R150) to R50i, a large number of known standard processes is suitable, for example alkylation, halogenation, acylation, amidation, oximation, oxidation and reduction, the choice of the suitable preparation processes depending on the properties (reactivities) of the substituents in the intermediates in question. The novel compounds of the formula lib in which Rf is trifluoromefriyl, difluorochloromethyl, pentafluoroethyl, heptafluoro-n-propyl or trichloromethyl, RXi is d-C6alkyl and Q and R are as defined under formula I can be prepared by generally known processes via 3-alkoxycarbonyl-4-perhaloalkyipyridine N-oxides of the formula XXVIII according to reaction scheme 5 by preparing, using suitable chlorination conditions and separation processes, the 6-chloro-4-haloalkyl-3-nicotinic esters of the formula XXX and then converting these compounds with a nucleophile of the formula XXXI Zo,-Risi (XXXI) in which Z01 is SH, hydroxyl, halogen or amino and R151 is hydrogen, C1-C6alkyl, C3-C6-alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, halogen, C3-C6haloalkynyl, CrC6alkylsulfonyl, d-C6-haloalkyl, phenyl, benzyl, where the phenyl and benzyl groups for their part may be substituted by d-C3alkyl, d-C3haloalkyl, CrC3alkoxy, CrC3haloalkoxy, halogen, cyano or nitro, is d-dalkoxy-d-dalkyl or CrC4alkylthio-C1-C4alkyl, C1-C4alkyisulfinyl-C1-C4alkyl, C1-C4alkylsulfonyl-C1-C4alkyl, or a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and the ring system for its part may be mono-, di- or trisubstituted by CrC6alkyl, d-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6-haloalkynyl, d-Cealkoxy, d-C6haloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, d-C6alkylthio, d-dhaloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5alkoxy-alkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-dcyanoalkylthio, d-C6-alkylsulfinyl, d-C6haloalkylsulfinyl, d-C6alkylsulfonyl, d-C6haloalkylsulfonyl, aminosulfonyl, d-C2alkylaminosulfonyl, C2-ddialkylaminosulfonyl, d-C3alkylene-R96, NR97R98, halogen, cyano, nitro, phenyl or benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by d-C3alkyl, d-C3haloalkyl, d-C3alkoxy, d-C3-haloalkoxy, halogen, cyano or nitro, R96 is d-C3alkoxy, C2-dalkoxycarbonyl, d-C3alkylthio, d-C3alkylsulfinyl, d-C3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by d-C3alkyl, d-C3haloalkyl, d-C3-alkoxy, d-C3haloalkoxy, halogen, cyano or nitro; t R97 is hydrogen or d-C6alkyl and Rg8 is d-C6alkyl or d-C6alkoxy; and where substituents on nitrogen in the heterocyclic ring are different from halogen, using reaction processses which are generally known to the person skilled in the art, into the 6- substituted 4-perhaloalkylnicotinic acids of the formula XXXII and their subsequent products of the formulae lib and lb as described in reaction scheme 1. This is shown in reaction scheme 6 below. According to this reaction scheme, it is preferably possible to prepare the compounds of the formula I with the group Q, in which R20 is hydroxyl, the compounds of the formula I with the group Q2 in which R23 is hydroxyl, the compounds of the formula I with the group Q3 in which R26 is hydroxyl and the* compounds of the formula I with the group Q4 in which R30 is hydroxyl. 6-substituted 2-haloalkylnicotinic acid compounds of the formula Ic can be prepared, for example, from the corresponding 2-haioalkyl-3-alkoxycarbonyl-2-pyridines XXXIII in which Rf is trifluoromethyl, difluorochloromethyl, pentafluoroethyl, heptafluoro-n-propyl'or trichloromethyl and R1x is C1-C6alkyl and R is as defined under formula I, by hydrolysis into the corresponding carboxylic acids and their subsequent activation, for example by conversion into an acyl haiide (lie). (Reaction scheme 7) Their precursors of the formulae XXXIIIa, XXXIIIb, XXXIIIc, XXXIIId, XXXIIIe, XXXIIIf, XXXIIIg and XXXIIIh are likewise accessible by conversion processes known to the person skilled in the art (reaction scheme 7). 2-Trifluoromethyl-3-ethoxycarbonyl-2-pyridone (formula XXXIIIa in which R is hydrogen, R1X is ethyl and Rf is trifluoromethyl) in particular is known from Org. Process Research & Development, 1, 370 (1997). Intermediates of the formulae XXXIIIa to XXXIIIh can be obtained by reacting, for example for preparing a 6-halo derivative of the formula XXXIIId, a pyridone of the formula XXXIIIa (preparation according to Org. Process Research & Development, 1, 370 (1997) or scheme 8) with a halogenating agent, for example phosphorus oxychloride, phosphorus oxybromide or phenyl dichlorophosphate, in the presence or absence of added base, such as a dialkylaniiine, in the presence or absence of solvent, if desired in a pressure vessel, at temperatures between 0 and 220°C (preferably 60-200°C). It is known to the person skilled in the art how to convert chloro derivatives by nucleophilic substitution, for exarnple using an alkali metal iodide in an inert solvent into the corresponding iodides, or using gaseous hydrobromic acid in lower carboxylic acids, for example cone, acetic acid, into the corresponding bromo derivatives (for example according to US-A-?,974,166) or using alkali metai fluoride in a dipolar solvent, such as sulfolane, into the corresponding fluoro derivatives. The compound of the formula XXXIIIe can be prepared by reacting a halo derivative of the formula XXXIIId obtained as described above with an alcohol of the formula R151-OH in the presence of a base, such as sodium hydride, or an alkali metal oxide or carbonate, or directly with an alkali metal alkoxide, in an inert solvent such as dimethylformamide or in an excess of the alcohol of the formula R151-OH which corresponds to the group to be introduced, at temperatures between -5 and 160°C, or by reacting, to prepare a corresponding 6-thioether of the formula XXXIIIe, analogously to what was described above, either the halide of the formula XXXIIId with a thiol of the formula R151-SH in the presence of a base such as sodium hydride or with an alkali metal salt of a thiol in an inert solvent at -10-150°C, or by preparing, starting from a pyridone XXXIIIa and using a thionating agent, for example Lawesson's reagent, in an inert solvent, such as toluene or acetonitrile, a pyrithione of the formula XXXIIIb and alkylating this with an alkylating agent Rl51-X, where X is a leaving group, such as halide (CI, Br, I) or ROS03- or RS02-, at 20-120°C in an inert solvent, such as tetrahydrofuran, to give the thioether of the formula XXXIIIe, or, to prepare the corresponding sulfinyl or sulfonyl derivative of the formula XXXIIIf, reacting with an oxidizing agent, such as m-chloroperbenzoic acid or sodium periodate, or sodium perborate, under temperature control known to the person skilled in the art, depending on the degree of oxidation (for example -30°C -+50CC for m0i =1 or -20°C - +100°C for m0i=2) in an inert solvent, such as dichioromethane, to give XXXIIIf, or, to prepare 6-alkyl derivatives XXXIIIg according to the invention, reacting a sulfone of the formula XXXIIIf (m0i =2) or a halo derivative of the formula XXXIIId in the presence or absence of a Pd(0) catalyst such as Pd(PPh3)2CI2 with a tetra-d-Cealkyltin or with a Grignard reagent CrC6alkyl-MgHal at temperatures between -10° and 180°C, for example analogously to Synlett 1998 (1185), or as described in Organocopper Reagents, R.J.K.Taylor, Oxford University Press 1994, or in Transition Metals in Organic Synthesis, S. Gibson, Oxford Univ. Press,1997, or in Org. React. 50, 1 (Stille reaction), or, to prepare 6-cyano derivatives of the formula XXXIIIh, reacting a halide of the formula XXXIIId or a sulfone of the formula XXXIIIf (m0i=2) with an alkali metal or tetraalkylammonium cyanide or copper cyanide in an inert solvent, such as dichloromethane, tetrahydrofuran or dimethylformamide, at temperatures between 0°C and 220°C. - Some of the compounds of the formula XXXIIIe are also obtainable from the pyridone of the formula XXXIIIa by reacting them analogously to Org. React. 42, 2 with an alcohol R151OH in the presence of an azodicarboxylic ester (for example diethyl ester) and triphenylphosphine in an inert solvent, such as tetrahydrofuran or dioxane. (Scheme 9) Reaction scheme 9: The intermediates of the formula XXXIIIa required in reaction scheme 8 as starting materials are obtainable according to Scheme 10 route A or route B (Org. Process Research & Development, I, 370 (1997)) or route C. Intermediates of the formula XXXIIIa are obtainable by route A by reacting, to prepare the 3,4-dihydro-5-alkoxycarbonyl-6-haloalkylpyridin-2-ones of the formula XXXVIII, an enamine of the formula XXXV in the presence or, preferably, in the absence of a solvent either in an excess of enamine or in the presence of a base, such as a tert-amine, with an acryloyl chloride of the formula XXXIV at temperatures between -10° and + 200°C, or by reacting a keto ester of the formula XXXVII with an acrylamide of the formula XXXVI in the presence of a catalyst such as p-toluenesulfonic acid (=HOTs) in an inert solvent, such as toluene, at temperatures between 30 and 200CC, with removal of the water of reaction formed (for example azeotropic distillation), or by reacting a keto ester of the formula XXXVII in the presence of a base, such as an alkali metal alkoxide or magnesium alkoxide, with a 4-halo-keto ester of the formula XXXIX in an inert solvent, such as ethanol, at 0-180cC to give the intermediate of the formula XXXX, converting this with ammonia or an ammonium salt, such as ammonium acetate, or with a bis-siiylamine such as hexamethyldisilazane, in the presence or absence of an acidic catalyst, such as sulfuric acid or p-toluenesulfonic.acictor an organic carboxylic acid (for example cone, acetic acid), in an inert solvent and at temperatures between 0° and 180°C into the corresponding enamine of the formula XXXXI, subsequently cyclizing in the presence of a catalyst, such as p-toluenesulfonic acid or sulfuric acid, if desired with continuous removal of the water of reaction formed in an inert solvent, such as toluene, to give the dihydropyridone of the formula XXXVIII, and finally treating with an oxidizing agent, such as manganese dioxide, in an inert solvent, such as chlorobenzene, at temperatures between 50 and 250°C, to prepare the pyridones XXXIIIa. The intermediates of the formula lla in which Qa is hydroxyl, halogen, cyano, or a group -CH2(CO)R36 or Rb is hydrogen, C1-C4aikyl or halogen; R, is trifluoromethyl, difluorochloromethyl, pentafluoroethyl, heptafluoro-n-propyl or trichloromethyl; Ra is C1-C3alkyl, CrCshaloalkyl, C3-C4cycloalkyl, C1-C2alkoxy-C1-C4alkyl, CrC2- t alkylthiomethyl, hydroxyl, halogen, cyano, d-C3alkoxy, C1-C3haloalkoxy, allyloxy, propargyloxy, d-C3alkylthio, CrC3alkylsulfinyl, CrC3alkylsulfonyl or CrC3alkylsulfonyloxy, and R0i and R36 are as defined under group Q5 of the formula I, except for the compounds 2,6-bistrifluoromethylnicotinic acid, 2,6-bistrifluoromethyl-5-methoxynicotinic acid and 2-hydroxy-6-trifluoromethylnicotinic acid, are novel and therefore likewise form part of the subject matter of the present invention. R99 is C1.C4alkyl, C1.C4haloalkyl, C3.C4cycloalkyl or d-C4alkoxy; R( is trifluoromethyl, difiuorochioromethyl, pentafluoroethyl or heptafluoro-n-propyl; and Rc is CrC3alkyl, d-Cahaloalkyl, C1-C2alkoxymethyl, CrC2alkylthiomethyl, hydroxyi, halogen, cyano, d-C3alkoxy, d-C3haloalkoxy, aliyioxy, propargyloxy, C1-C3aikylthio, d-C3- alkylsulfinyl, C1-C3alkylsulfonyl or C1-C3alkylsulfonyloxy and R01 is as defined under formula I are novel and therefore likewise form part of the subject matter of the present invention. The compounds of the formula I or compositions comprising them can be used according to the invention in all.the,application methods customary in agriculture, for example pre-emergence application, postemeTgence application and seed dressing, and various methods and techniques, for example controlled release of active compounds. To this end, the active compound is absorbed in solution onto mineral granule carriers or polymerized granules (urea/formaldehyde) and dried. If appropriate, a coating which allows the active compound to be released in metered form over a certain period of time can additionally be applied (coated granules). The compounds of the formula I can be employed as herbicides in unchanged form, i.e. as they are obtained in the synthesis, but they are preferably processed in a customary manner with the auxiliaries conventionally used in the art of formulation, for example to give emulsifiable concentrates, directly sprayable or dilutable solutions, dilute emulsions, wettable powders, soluble powders, dusts, granules or microcapsules. Such formulations are described, for example, in WO 97/34485 on pages 9 to 13. The methods of application, such as spraying, atomizing, dusting, wetting, scattering or watering, in the same way as the nature of the compositions, are chosen according to the aims striven for and the given circumstances. The formulations, i.e. the compositions, formulations or preparations comprising the active compound of the formula I or at least one active compound of the formula I and as a rule one or more soJid or liquid formulation auxiliaries, are prepared in a known manner, for example by intimate mixing and/or grinding of the active compounds with the formulation auxiliaries, for example solvents or solid carriers. Surface-active compounds (surfactants) can furthermore additionally be used during the preparation of the formulations. Examples of solvents and solid carriers are given, for example, in WO 97/34485 on page 6. Depending on the nature of the active compound of the formula I to be formulated, suitable surface-active compounds are nonionic, cationic and/or anionic surfactants and surfactant mixtures having good emulsifying, dispersing and wetting properties. Examples of suitable anionic, nonionic and cationic surfactants are listed, for example, in WO 97/34485 on pages 7 and 8. The surfactants conventionally used in the art of formulation and which are suitable to .prepare the herbicidal compositions according to the invention-are described, inter alia, in "Mc Cutcheon's Detergents and Emulsifiere Annual", MC Publishing Corp., Ridgewood New Jersey, 1981, Stache, H., "Tensid-Taschenbuch" [Surfactant handbook], Carl Hanser Verlag, Munich/Vienna, 1981 and M. and J. Ash, "Encyclopedia of Surfactants", Vol l-lll, Chemical Publishing Co., New York, 1980-81. The herbicidal formulations as a rule comprise 0.1 to 99% by weight, in particular 0.1 to 95% by weight, of herbicide, 1 to 99.9% by weight, in particular 5 to 99.8% by weight, of a solid or liquid formulation auxiliary and 0 to 25% by weight, in particular 0.1 to 25% by weight, of a surfactant. While concentrated compositions are rather preferred as commercial goods, the end user as a rule uses dilute compositions. The compositions can also comprise further additives, such as stabilizers, for example epoxidized or non-epoxidized vegetable oils (epoxidized coconut oil, rapeseed oil or soya oil), defoamers, for example silicone oil, preservatives, viscosity regulators, binders, tackifiers and fertilizers or other active compounds. The active compounds of the formula I are as a rule applied to the plants or their habitat, at application rates of 0.001 to 4 kg/ha, in particular 0.005 to 2 kg/ha. The dosage required for the desired effect can be determined by tests. It depends on the nature of the effect, the development stage of the crop plant and the weed and on the application (location, time, process) and can, as a function of these parameters, vary within wide ranges. The compounds of the formula I have herbicidal and growth-inhibiting properties, owing to which they can be used in crops of useful plants, in particular in cereals, cotton, soya, sugar beet, sugar cane, plantings, rapeseed, maize and rice, and for the non-selective control of weeds. Crops include those which have been rendered tolerant towards herbicides or » herbicide classes by conventional breeding methods or genetical engineering methods. The weeds to be controlled can be both monocotyledonous and dicotyledonous weeds, for example Stellaria, Nasturtium, Agrostis, Digitaria, Avena, Setaria, The examples below illustrate the invention in more detail, without limiting it. »*> • '-■ • * - • •■ •. Preparation Examples: ' *r ' Example H1: Preparation of 2-difluoromethoxv-6-trifluoromethvlnicotinic acid: At 70°C, 25 g (0.106 mol) of (3-(ethoxycarbonyl)-6-trifluoromethyl)pyrid-2-one (Helv. Chim. Acta (1988), 71(3), 596-601) in a mixture of 50 ml of dimethylformamide and 20 ml of water are treated, in the presence of 16 g (0.116 mol) of finely powdered potassium carbonate and with efficient stirring, with a continuous stream of gaseous Freon-22. After 6 hours, a further 16 g of potassium carbonate and 20 ml of dimethyl sulfoxide are added, and the mixture is stirred with continuous introduction of Freon-22 gas at a temperature of 100°C for another 4 hours. The mixture is then treated with water and ice and extracted with diethyl ether. The aqueous phase is adjusted to pH 2 using cone. HCI and extracted with ethyl acetate. Diethyl ether is added to the extract, and some (3-(carboxy)-6-trifiuoromethyl)pyrid-2-one crystals which have precipitated out are removed by filtration. The filtrate is filtered through a silica gel column (mobile phase ethyl acetate/hexane 1:1) giving, as a crystalline product, pure 2-difluoromethoxy-6-trifluoromethylnicotinic acid: 1H NMR (CDCI3, ppm): 8.60, d, J=9 Hz, 1H; 7.62, d, J=9 Hz , 1H; 7.62, t, J=67 Hz, 1H. Example H2: Preparation of 4-methvl-6-trifluoromethvlnicotinic acid: In the presence of 5.8 ml of phenyl dichiorophosphate, 7.5 g (0.03 mol) of ((3-ethoxycarbonyl)-4-methyl-6-trifluoromethyl)pyrid-2-one (Helv. Chim. Acta (1988), 71(3), 596-601) are heated in a pressure vessel at a temperature of 170°C for 3 hours. The cold reaction solution is filtered directly through a short silica gel column (mobile phase: ethyl acetate/hexane 1:9), giving, as an oily product, ethyl 2-chloro-4-methyl-6-trifluoromethyl-pyridin-3-ylcarboxylate: 1H NMR (CDCI3, ppm): 7.49, s, 1H; 4.48, q, 2H; 2.43, s, 3H, 1.43, t, 3H. 3.0 g (16.8 mmol) of the above product and, in 2 portions, a total of 5 g of ammonium formate are added to a suspension of 0.55 g of 10% Pd/C in 20 ml of methanol, and the mixture is stirred at room temperature for 24 hours. The reaction mixture is then filtered through Celite and, after addition of sodium chloride solution, extracted with ethyl acetate. Chromatographic purification (mobile phase 1:9) gives the 4-methyl-6-trifluoromethylpyridin-3-yl ethyl ester as an oil: 1H NMR (CDCI3, ppm): 9.11, s, 1H; 7.56, s, 1H, 4.44, q, 2H; 2.72, methanethiolate (0.33 g) until no further conversion can be detected by gas chromatographic analysis. The mixture is then filtered through silica gel and evaporated. This gives-Q.73 g of methyl 6-me*chylthio-4-trifluoromethylpyridin-3-ylcarboxylate; 1M NMR (CDCI3, ppm): 8.98, s, 1H; 7.48, s, 1H; 3.94, s, 3H; 2.64, s, 3H. Hydrolysis under the conditions mentioned above gives 6-methylthio-4-trif luoromethyl-nicotinic acid: 1H NMR (CDCI3, ppm): 9.02, s, 1H;7.46, s, 1H; 2.64, s, 3H. Example H5: 6-Hvdroxv-2-trifluoromethvtpvridin-3-vl ethyl ester: Under an atmosphere of nitrogen and with stirring, 33.4 g of 3,4-dihydro-5-ethoxycarbonyl-6-trifluoromethylpyridin-2-one (Org. Res.& Devel. 1,370 (1997)) and 34 g of manganese dioxide in 250 ml of 1,2-dichlorobenzene are heated under reflux for 24 hours. In intervals of about 20 hours, manganese dioxide (total amount of Mn02 used: 213 g) is added six more times over a period of 3 days, and the mixture is in each case heated further under reflux. The mixture is then cooled, diluted with ethyl acetate, and filtered through silica gel, the filtercake is washed with ethyl ester and the filtrate is concentrated. The solid residue (26.7 g, i.e. 80%), which may still contain about 6% of starting material, is directly reacted further. For complete purification, it is possible to purify, for example, over silica gel (hexane/ethyl acetate 7:3) (1H NMR, CDCI3, ppm): 8.02 (d, 1H); 6.85 (d, 1H); 4.86 (q, 2H); 1.37 (t, 1H). Example H6: Preparation of ethyl 6-chloro-2-trifluoromethvlpyridin-3-vlcarboxvlate: In a bomb tube, 23.5 g of ethyl 6-hydroxy-2-trifluoromethylpyridin-3-ylcarboxylate and 23.5 ml of phenyl dichlorophosphate are heated at 170°C for 3 hours, and the mixture is, after cooling, added to ice-water, stirred for a few minutes and subsequently taken up in ethyl acetate and made slightly alkaline using sodium bicarbonate and then washed neutral t with water. The extracts are admixed with a little hexane and filtered through silica gel. The filtrate is evaporated, leaving 21.6 g (85%) of the title compound in the form of a dark oil with nD301.4679. 1H NMR (CDCI3, ppm): 8.09 (d,1H); 7.60 (d,1H);/4.43 (q, 2H); 1.43 (t,3H). s, 3H, 1.42, t, 3H. This is hydrolysed at 40°C in the presence of aqueous potassium hydroxide solution in dioxane. Extraction-with ethyl acetate gives, after acidification to pH 2.7, 4-methyl-6-trifluoromethylnicotinic acid as a crystalline product: 1H NMR (CDCI3, ppm): 7.49, s, 1H; 4.48, q, 2H; 2.43, s, 3H, 1.43, t, 3H; 9.32, s, 1H, 7.62, s, 1H, 2.79, s, 3H. Example H3: Preparation of 6-chloro-4-trifluoromethvlnicotinic acid: 9.6 g (0.047 mol) of methyl 4-trifluoromethylpyridin-3-ylcarboxylate, dissolved in 50 ml of dichloromethane, are treated with 30% hydrogen peroxide/urea adduct and 17 ml of trifluoroacetic anhydride. The reaction solution is stirred at temperature of 20°C for 20' hours and then washed once each with dilute sodium hydroxide solution and half-saturated sodium chloride solution. The product obtained is 3-methoxycarbonyl-4-trifluoromethyl-3-pyridine N-oxide; 1H NMR (CDCI3, ppm): 8.55, s, 1H; 8.31, d, 1H; 7.6, d, 1H; 3.98, s, 3H. 4.85 g (0.022 mol) of the above product are then added to a mixture of 5 ml of phosphorus oxychloride and 4.3 ml of ethyldiisopropylamine in 15 ml of 1,2-dichloroethane, and the mixture is heated to a temperature of 60°C. After about 2 hours, another 2 ml of phosphorus oxychloride and 2.8 ml of ethyldiisopropylamine are added, and the mixture is stirred at this temperature for 20 hours. The reaction mixture is subsequently added to ice-water, adjusted to pH 3 using 30% NaOH and then extracted with dichloromethane. Filtration through a little silica gel gives an approximately 5:1 product mixture of the two 6-chloro- and 2-chloro-4-trifluoromethylpyridin-3-yl methyl esters, which can be separated by HPLC into the pure components. Thus, pure methyl 6-chloro-4-trifluoromethylpyridin-3-ylcarboxylate is obtained as the main product; 1H NMR (CDCI3, ppm): 8.91, s, 1H; 7.68, s, 1H; 3.98, s, 3H, and pure methyl 2-chloro-4-trifluoromethylpyridin-3-ylcarboxylate is obtained as the byproduct; 'H NMR (CDCI3, ppm): 8.64, d, 1H; 7.52, d, 1H; 4.01, s, 3H. In the presence of 0.073 g of potassium hydroxide, 0.22 g of pure methyl 6-chloro-4-trifluoromethyipyridin-3-ylcarboxylate are hydrolysed at room temperature in a 1:1 mixture of t 6 ml of dioxane/water. Recrystallization gives the pure 6-chloro-4-trifluoromethylnicotinic acid: m.p. 115-117°C; 'H NMR (CDCI3, ppm): 9.12, s, 1H; 7.24, s, 1H. i Example H4: Preparation of 6-methvlthio-4-trifluoromethvlnicotinic acid: In boiling acetone, 0.70 g (2.9 mol) of methyl 6-chloro-4-trifluoromethylpyridin-3-ylcarboxylate is treated in the presence of a catalytic amount of 18-crown-6 with methanethiolate (0.33 g) until no further conversion can be detected by gas chromatographic analysis. The mixture is then filtered through -silica gel and evaporated. This gives 0.73 g of methyl 6-methylthio-4-trifluoromethylpyridirr-3-ylcarboxylate; 1H NMR (CDCI3, ppm): 8.98, s, 1H; 7.48, s, 1H; 3.94, s, 3H; 2.64, s, 3H. Hydrolysis under the conditions mentioned above gives 6-methylthio-4-trifluoromethyl-nicotinic acid: 1H NMR (CDCI3, ppm): 9.02, s, 1H; 7.46, s, 1H; 2.64, s, 3H. Example H5: 6-Hvdroxv-2-trifluoromethvlpvridin-3-vl ethyl ester: Under an atmosphere of nitrogen and with stirring, 33.4 g of 3,4-dihydro-5-ethoxycarbonyl-6-trifluoromethylpyridin-2-one (Org. Res.& Devel. 1,370 (1997)) and 34 g of manganese dioxide in 250 ml of 1,2-dichlorobenzene are heated under reflux for 24 hours. In intervals of about 20 hours, manganese dioxide (total amount of Mn02 used: 213 g) is added six more times over a period of 3 days, and the mixture is in each case heated further under reflux. The mixture is then cooled, diluted with ethyl acetate, and filtered through silica gel, the filtercake is washed with ethyl ester and the filtrate is concentrated. The solid residue (26.7 g, i.e. 80%), which may still contain about 6% of starting material, is directly reacted further. For complete purification, it is possible to purify, for example, over silica gel (hexane/ethyl acetate 7:3) (1H NMR, CDCI3, ppm): 8.02 (d, 1H); 6.85 (d, 1H); 4.86 (q, 2H); 1.37 (t, 1H). Example H6: Preparation of ethyl 6-chloro-2-trifluoromethvlpvridin-3-vlcarboxvlate: In a bomb tube, 23.5 g of ethyl 6-hydroxy-2-trifluoromethylpyridin-3-ylcarboxylate and 23.5 ml of phenyl dichiorophosphate are heated at 170°C for 3 hours, and the mixture is, after cooling, added to ice-water, stirred for a few minutes and subsequently taken up in ethyl acetate and made slightly alkaline using sodium bicarbonate and then washed neutral with water. The extracts are admixed with a little hexane and filtered through silica gel. The filtrate is evaporated, leaving 21.6 g (85%) of the title compound in the form of a dark oil with nD30 1.4679. 'H NMR (CDCI3, ppm): 8.09 (d,1H); 7.60 (d,1H);/*.43 (q, 2H); 1.43 (t,3H). Example H7: Preparation nf fi.chloro-2-trifluoromethylpYridin-3-vlcarboxvlic acid: 2.5 g of the ethyl 6-chloro-2-trifluoromethyipyridin-3-yicarboxylate obtained above are dissolved in the smallest possible amount of tetrahydrofuran, treated with approximately 20 g of ice and 11 ml of 1N lithium hydroxide and stirred at room temperature until hydrolysed completely. The mixture is then washed with a little ether and the aqueous phase is acidified using 4N hydrochloric acid and extracted with ethyl acetate. The extracts are washed with sodium chloride solution, dried and evaporated. This gives 1.8 g of the title compound of m.p. 154-156°C. The other free carboxylic acids are likewise obtained from their esters in this manner. Example H8: Preparation of ethyl 6-methvlthio-2-trifluoromethvlpyridin-3-vlcarboxvlate: Under an atmosphere of nitrogen and with stirring, a solution of 1.7 g of 6-chloro-2-trifluoromethyipyridin-3-yl ethyl ester in 60 ml of dimethylformamide is treated a little at a time with 0.52 g of sodium methanethiolate and stirred at room temperature until the reaction has gone to completion. The reaction mixture is then poured into ice-water, made neutral by addition of a little dilute hydrochloric acid and extracted with ethyl acetate. The extracts are diluted with a little hexane, washed with water, dried over sodium sulfate, filtered and, after filtration through a little silica gel, evaporated. This gives 1.4 g (79%) of the title compound in the form of an oil with nD251.5100, 1H NMR (CDCI3, ppm): 7.90 (d, 1H); 7.40 (d, 1H); 1.40 (q, 2H); 2.60 (s, 3H); 1.49 (t, 3H). Example H9: Preparation of ethyl 6-ethylthio-2-trifluoromethvlpyridin-3-vicarboxvlate: In an apparatus previously flushed with nitrogen, a solution of 1.8 ml of ethanethiol in 40 ml of dimethylformamide, which had been cooled to 0°C, is treated a little at a time with 0.96 g of sodium hydride oil dispersion (60%), and the mixture is stirred at room temperature. After evolution of hydrogen has ceased, the mixture is cooled to -20°C, and a solution of 5.07 g of 6-chloro-2-trifluoromethylpyridin-3-yl ethyl ester in 10 ml of dimethylformamide is added dropwise at this temperature, and the mixture is stirred slowly until room temperature has been reached. After the reaction has ended (approximately 3 hours), the reaction mixture is added to ice-water and extracted with ethyl acetate. The extracts are washed with water, dried, filtered, evaporated and dried under high vacuum. This gives 5.0 g (89%) of the title compound as a brownish oil. 1H NMR (CDCI3, ppm): 7.90 (d, 1H); 7.35 (d, 1H); 4.40 (q, 2H); 3.25 (q,42H); 1-38 (2t, 6H). Example H10: Preparation of ethyl 6-ethvlsulfinvl-2-trifluoromethvlpvridin-3-vlcarboxvlate: Under an atmosphere of nitrogen and with stirring and cooling, a solution of 2.5 g of m-chloroperbenzoic acid in 40 ml of methylene chloride is added dropwise at a temperature of -20°C to a solution of 2.8 g of ethyl 6-ethylthio-2-trifluoromethylpyridin-3-ylcarboxylate, which had been charged initially, and the mixture is stirred at a temperature of +5°C for 20 hours. The mixture is then evaporated gently and purified over silica gel (hexane/ethyl acetate 7:3). This gives 2.48 g (84%) of 6-ethylsulfinyl-2-trifluoromethylpyridin-3-yl-ethyl ester. 1H NMR (CDCI3, ppm): 8.38 (d, 1H); 8.30 (d, 1H); 4.45 (q, 2H); 3.26 - 3.00 (m, 2H); 1.43 (t,3H); 1.26 (t,3H). Ethyl 6-methylsulfinyl-2-trifluoromethyipyridin-3-ylcarboxylate is obtained in an analogous manner. Example H11: Preparation of ethyl 6-methvlsulfonvl-2-trifluoromethvlpvridin-3-vtcarboxvlate: Under an atmosphere of nitrogen and with stirring and cooling, 21 g of m-chloroperbenzoic acid are introduced a little at a time over a period of 30 minutes at a temperature of -20°C into a solution of 3.6 g of 6-methylthio-2-trifluoromethylpyridin-3-yl ethyl ester, which had been charged initially, and the reaction mixture is stirred at room temperature for 5 hours. The mixture is then evaporated and filtered through silica gel (ethyl acetate/methanol/ triethylamine 85:10:5). This gives 3.95 g (97%) of ethyl 6-methy!sulfonyl-2-trifluoromethylpyridin-3-ylcarboxylate as a brownish solid with m.p. 70-72°C. 1H NMR (CDCI3, ppm): 8.40 (1H,d); 8.33 (lH,d); 4.47 (2H,q); 1.43 (3H,t). Example H12: Preparation of ethyl 6-cvano-2-trifluoromethvlpvridin-3-vlcarboxvlate: Under an atmosphere of nitrogen and with stirring, a solution of 0.596 g of ethyl 6-methylsulfonyl-2-trifluoromethylpyridin-3-ylcarboxylate in 5 ml of dimethylformamide is treated with 160 mg of solid potassium cyanide and a spatula tipful of 18-crown-6, and the mixture is heated at 80°C for 3 hours. The mixture is cooled overnight, and the next day another 30 mg of potassium cyanide are added and the mixture is heated further until the ». ..starting material has disappeared (approximately 2 hours). The mixture is then cooled, added to ice-water and extracted with ethyl acetate. The extracts are washed with water, dried, evaporated and freed from traces of dimethylformamide under high vacuum at approximately 40°C. This gives 480 mg (yield virtually quantitative) of ethyl 6-cyano-2-trifluoromethylpyridin-3-ylcarboxylate in the form of an oil which slowly solidifies. 1H NMR (CDCI3, ppm): 8.29 (1 H,d); 7.97 (1 H,d); 4.48 (2H, d); 1.43 (3H,t). Example H13: Preparation of ethvl 6-methvl-2-trifluoromethvlpvridin-3-vlcarboxylate: Under an atmosphere of nitrogen and with stirring, a solution of 3.6 g of 6-chloro-2-trifluoromethylpyridin-3-yl ethyl ester in 20 ml of dimethylacetamide is treated with 4.5 ml of tetramethyltin and 200 mg of dichloro(bistriphenylphosphine)palladium, and the mixture is heated to a temperature of 80-90°C for 24 hours. Then another 1.5 ml of tetramethyltin and 30 mg of dichloro(bistriphenylphosphine)palladium are added and the mixture is heated for another 6 hours. The reaction mixture is then freed from excess tetramethyltin using reduced pressure (destruction by passing through ethanolic sodium hydroxide solution), cooled and added to ice-water. The mixture is extracted with diethyl ether and the extract is washed with water, dried over sodium sulfate, filtered through a little silica gel, evaporated and dried under reduced pressure. This gives the title compound (2.4 g, 73%), which still contains traces of dimethylacetamide, in the form of a dark oil. 1H NMR (CDCI3, ppm): 8.00 (1H,d); 7.42 (1H,d); 4.42 (2H, d); 2.68 (3H, s); 1.41 (3H,t). Hydrolysis analogously to the description already mentioned above affords 6-methyl-2-trifluoromethylpyridin-3-ylcarboxyiic acid (brown resin) which is directly converted further into the carbonyl chloride. Example H14: Preparation of 6-methvl-2-trifluoromethvlpyridin-3-vlcarbonvl chloride: A solution of 0.45 g of 6-methyl-2-trifluoromethylpyridin-3-ylcarboxylic acid in 20 ml of dichloromethane is charged initially, 3 drops of dimethylformamide are added and the mixture is subsequently treated with 1.6 ml of oxalyl chloride. After the intensive evolution of gas has ceased, the mixture is kept at a bath temperature of 40°C for another 1.5 hours and then evaporated. The crude product (0.56 g) that remains as residue can be directly reacted further. 1H NMR (CDCI3, ppm): 8.20 (1H,d); 7.51 (1H,d); 2.65 (3H, s). Example H15: Preparation nf 4-oxobicvclof3.2.1]oct-2-en-2-vl 6-methyl-2-trifluoromethvl-nicotinate: Under an atmosphere of nitrogen and with stirring and cooling, a solution of 0.56 g of 6-methyl-2-trifluoromethylpyridin-3-ylcarbonyl chloride in 10 ml of methylene chloride is added dropwise at 0°C to a solution of 0.4 g of bicycio[3.2.1]octane-2,4-dione and 0.72 g of triethylamine in 10 ml of methylene chloride, and the mixture is stirred for 5 hours until room temperature has been reached. The mixture is then diluted with methylene chloride, washed with cold 1N hydrochloric acid, dried and evaporated to give the desired enol ester (0.8 g) as a brown resin which is directly reacted further. 1H NMR (CDCI3l ppm): 8.17 (1H,d); 7.51 (1H, d); 5.96 (1H, s); 3.04 (2H, m); 2.75 (3H, s); 2.32-1.30 (m). Example H16: Preparation of 4-hvdroxv-3-(6-methvl-2-trifluoromethvlpvridin-3-carbonvl)-bicyclo[3.2.1 loct-3-en-2-one: Under an atmosphere of nitrogen and with stirring, 0.8 g of the above enol ester is dissolved in 30 ml of acetonitrile at 25 °C, and the mixture is treated with 0.5 ml of triethylamine and 0.4 mi of acetone cyanohydrin and stirred at room temperature for 20 hours. The mixture is then diluted with solvent and washed with dilute hydrochloric acid, dried and evaporated, and the residue is purified through a little silica gel (ethyl acetate/methanol/triethylamine 85:10:5). This gives 371 mg (46%) of the title compound (triethylamine salt) in the form of a yellowish resin. 1H NMR (CDCI3, ppm): 7.45 (1H, d); 7.25 (1H, d); 3.80-3.43 (4H, m); 3.18 (6H, m); 2.80 (2H, s(br)); 2.62 (3H, s); 2.20-1.54 (m). Example H17: Preparation of ethyl 6-methoxv-2-trifluoromethvlpyridin-3-vlcarboxvlate: t A suspension of 5.65 g of ethyl 6-hydroxy-2-trifluoromethylpyridin-3-ylcarboxylate, 6.0 g of potassium carbonate and 2.7 ml of methyl iodide is, together with a spatula tipful of 18-crown-6, heated to a temperature of 60-70cC until the reaction ha£ gone to completion. The mixture is then filtered, the filtration residue is washed with acetonitrile and the filtrate is concentrated under reduced pressure. The residue is cooled, admixed with ice-water, neutralized with dilute sulfuric acid and extracted with ethyl acetate. The extracts are washed with water, dried, diluted with a little hexane and filtered through a little silica gel. The resulting residue is the title compound (3.7 g, 65%) in the form of slightly orange crystals of m.p. 150-152°C. 1H NMR (CDCI3, ppm): 8.00 (1H, d); 6.83 (1H, d); 4.38 (2H, q); 4.01 (3H, s);1.39 (3H, t). Example H18: Preparation of 4-hvdroxv-3-(2-methvl-6-trifluoromethylpvridin-3<:arbonv0-bicvclof3.2.11oct-3-en-2-one:> 6.68 g (0.0305 mol) of methyl 2-methyl-6-trifluoromethylnicotinate (prepared as described in Heterocycles, 46, 129 (1997)) are dissolved in 250 ml of methanol/water (3:1 mixture), and 1.92 g (0.046 mol) of lithium hydroxide hydrate are added a little at a time at 22°C. After 4 hours at 22°C, the reaction mixture is poured into ethyl acetate and 2 N hydrochloric acid, the organic phase is washed three times with water, dried with sodium sulfate and evaporated and the residue is triturated with a little hexane. Filtration gives 5.69 g (90% of theory) of the expected 2-methyl-6-trifluoromethylnicotinic acid of m.p. 147-149°C. The 2-methyl-6-trifluoromethylnicotinic acid obtained (2.0 g, 0.0098 mol) is dissolved in 20 ml of oxalyl chloride. Three drops of dimethylformamide are added, and the mixture is heated under reflux for 1 hour. The mixture is then concentrated using a rotary evaporator, and the residue (2-methyl-6-trifluoromethylnicotinoyl chloride) is taken up in 30 ml of methylene chloride. At 0°C, 2.7 ml (0.0196 mol) of triethyiamine and 0.12 g (0.00098 mol) of dimethylaminopyridine are added. 1.49 g (0.0108 mol) of bicyclo[3.2.1]octane-2,4-dione, dissolved in 20 ml of methylene chloride, are then added dropwise. After 3 hours at 22CC, the reaction mixture is extracted with 2 N hydrochloric acid. The methylene chloride phase is separated off, washed with water and subsequently extracted with 10% aqueous sodium bicarbonate solution, dried over sodium sulfate and evaporated. This gives 3.18 g (100% of theory) of 4-oxobicyclo[3.2.1]oct-2-en-2-yl 2-methyl-6-trifluoromethylnicotinate as an oil, which can be processed further without purification. 3.02 g (0.0093 mol) of 4-oxobicycio[3.2.1]oct-2-en-2-yl 2-methyl-6-trifluoromethylnicotinate t and 1.9 ml (0.0136 mol) of triethyiamine are dissolved in 45 ml of acetonitrile. At 22°C, 0.01 ml of acetone cyanohydrin are added. After 18 hours at 22CC, the reaction mixture is poured into dilute hydrochloric acid and extracted with ethyl acetate. The ethyl acetate phase is washed with water and then with brine, dried over sodium sulfate and evaporated, and the residue is dissolved in a little warm acetone. The product crystallizes on standing. Filtration gives 0.99 g (33% of theory) of the expected 4-hydroxy-3-(2-methyl-6- trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one as white crystals (m.p. 75-77°C). Example H19: Preparation of 3-(2-methvl-6-trifluoromethvlpvridine-3-carbonyl)-4-oxo-bicvclor3.2.11oct-2-en-2-yl benzoate: At 0°C, a solution of 0.562 g (0.0004 mol) of benzoyl chloride in 1 ml of tetrahydrofuran is added to a solution of 1.14 g (0.0035 mol) of 4-hydroxy-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one and 0.517 g (0.004 mol) of ethyldiisopropylamine in 15 ml of tetrahydrofuran. The reaction mixture is stirred at 25°C for 2 hours, evaporated and purified over silica gel (hexane/ethyl acetate 1:1). This gives 0.9 g (60%) of the title compound in the form of a yellowish resin. 1H NMR (CDCI3, ppm): 7.91-7.87, m, 3H; 7.64, t, J=7.5 Hz, 1H; 7.50-7.40, m, 3H; 3.24, brt, J=4 Hz, 1H; 3.14, brt, J=4 Hz, 1H; 2.70, s, 3H; 2.47, d, J=13.5 Hz, 1H; 2.40, 2.15, m, 3H; 1.95-1.8, m, 2H. Example H20: Preparation of 4-hvdroxv-3-(2-methvl-1-oxv-6-trifluoromethvlpyridine-3-carbonvl)bicvclof3.2.1]oct-3-en-2-one: 16.25 g (0.05 mol) of 4-hydroxy-3-(2-methyl-6-trifluoromethyipyridine-3-carbonyl)-bicyclo[3.2.1]oct-3-en-2-one and 9.4 g (0.1 mol) of urea/hydrogen peroxide complex are dissolved in 150 ml of methylene chloride, and 20.5 mi (0.15 mol) of trifluoroacetic anhydride are added dropwise at 25°C. After 14 hours at 25°C, the reaction mixture is added to ethyl acetate and water, and the organic phase is washed twice with water, dried with sodium sulfate and evaporated. The residue is chromatographed over silica gel (mobile phase: ethyl acetate/methanol 9/1). This gives 6.8 g (40%) of the desired product as white crystals (m.p. 109-110°C). Example H21: Preparation of 4-chloro-3-(2-methvl-6-trifluoromethvlpvhdine-3-carbonvl)-bicyclo[3.2.1 ]oct-3-en-2-one: 20.15 g (0.062 mol) of 4-hydroxy-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)-bicyclo[3.2.1]oct-3-en-2-one are suspended in 50 ml of oxalyl chloride, and 0.1 ml of dimethylformamide are added dropwise. After the intensive evolution of gas has ceased, the mixture is kept at a bath temperature of 45°C for another 1.5 hours and then evaporated, and the residue is suspended in a little ethyl acetate and admixed with stirring at 0°C with hexane. Filtration gives 19.19 g (90% of theory) of ■4-chloro-3-(2-methyl-6-trifluoromethyl-pyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one of m.p. 137-T38°C. Example H22: Preparation of 4-amino-3-(2-methvl-6-trifluoromethvlpvridine-3-carbonyl)-bicvclof3.2.11oct-3-en-2-one: 1.0 g (0.0029 mol) of 4-chloro-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)-bicyclo[3.2.1]oct-3-en-2-one are dissolved in 10 ml of tetrahydrofuran and, at 25°C, treated with 2.0 ml of aqueous ammonia (30%). After 0.5 hours at 25°C, the reaction mixture is added to ethyl acetate and water, the organic phase is washed twice with water, dried with sodium sulfate and evaporated and the residue is triturated with a little ethyl acetate. Filtration gives 0.81 g (86% of theory) of 4-amino-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one in the form of white crystals (m.p. 262-263°C). 1H NMR (CDCI3, ppm): 10.62 br s 1H; 8.223 br s 1H; 7.41, d, J= 8.1 Hz, 1H;7.35, d, J= 8.1 Hz, 1H; 3.03, br t, J= 4.8 Hz, 1H; 2.70, br t, J= 4.8 Hz, 1H; 2.41, s, 3H; 1.97-2.14, m, 3H; 1.77-1.812, m, 1H; 1.47-1.70, m, 2H. Example H23: Preparation of 4-(4-chlorophenvlsulfanvl)-3-(2-methvl-6-trifluoromethyl-pvridine-3-carbonv0bicvclor3.2.11oct-3-en-2-one: 2.0 g (0.0058 mol) of 4-chloro-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)-bicyclo[3.2.1]oct-3-en-2-one, 0.07 g of dimethylaminopyridine (0.00058 mol) and 1.61 ml of triethylamine are dissolved in 15 ml of methylene chloride. At 25°C, 0.092 g (0.0064 mol) of 4-chlorothiophenol are added. After 2 hours at 22°C, the reaction mixture is evaporated and purified over silica gel (hexane/ethyl acetate 2:1). Recrystallization (hexane/acetic acid at -25°C) gives pure 4-(4-chlorophenylsulfanyl)-3-(2-methyl-6-trifluoromethylpyridine-3- » carbonyl)bicyclo[3.2.1]oct-3-en-2-one: m.p. 130-131 °C. Example H24: Preparation of 4-(4-chlorobenzenesulfonvl)-3-(2-methvl-6-trifluoromethyl-pvhdine-3-carbonvl)bicvclof3.2.1]oct-3-en-2-one: 0.6 g (0.00133 mol) of the 4-(4-chlorophenylsulfanyi)-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one obtained above is dissolved in methylene chloride, and 0.9 ml of peracetic acid (39% in acetic acid, 0.0053 mol) are added dropwise at 25°C. After 5 hours at 25°C, the reaction mixture is added to ethyl acetate and water, the organic phase is washed with water, dried with sodium sulfate and evaporated and the residue is triturated with a little hexane. Filtration gives 0.56 g (84% of theory) of 4-(4-chlorobenzenesulfonyl)-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one in the form of white crystals (m.p.166-167°C). Example H25: Preparation of (5-cvclopropvl-3-methvlsulfanvlisoxazol-4-vlH2-methvl-6-trifluoromethvlpvridin-3-vl)methanone and cvclopropvK3-methvlsulfanvl-5-(2-methvl-6-trifluoromethvlpvridin-3-vl)isoxazol-4-yllmethanone: 14.8 g (0.080 mol) of tert-butyl 3-cyclopropyl-3-oxopropionic acid ester are dissolved in 25 ml of MeOH, and 1.93 g (0.080 mol) of magnesium are added. With ice-bath cooling, 7 ml of carbon tetrachloride are added dropwise, and the reaction mixture is stirred at a temperature of 22°C for one hour. After evaporation, the residue is suspended in 100 ml of acetonitrile, and 16.31 g (0.073 mol) of 2-methyl-6-trifluoromethylnicotinoyl chloride (prepared as described in Example H18), dissolved in 50 ml of acetonitrile, are added dropwise at a temperature of 22CC. After 6 hours, the reaction mixture is taken up in ethyl acetate and washed with saturated sodium bicarbonate solution. The ethyl acetate phase is separated off, washed with water, dried over sodium sulfate and evaporated. The residue is dissolved in 160 ml of methylene chloride, and 10 ml of trifluoroacetic acid are added dropwise at a temperature of 22°C. After 18 hours, the reaction mixture is poured into water and extracted with methylene chloride. The methylene chloride phase is washed with water and then with saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated. This gives 17.3 g (88% of theory) of 1-cyclopropyl-3-(2-methyl-6-trifluoromethylpyridin-3-yi)propane-1,3-dione as an oil, which is processed further without purification. The 1 -cyclopropyl-3-(2-methyl-6-trifluoromethylpyridin-3-yl)propane-1,3-dione obtained above (15.0 g, 0.055 mol) is dissolved in 150 ml of dimethylformamide, and 50 g of potassium fluoride on an aluminium oxide support (alumina) (0.0055 mol/g, 0.276 mol) are added a little at a time at a temperature of 0°C. After 5 minutes, 6.7 g (0.088 mol) of carbon disulfide are added dropwise. After 2 hours, 23.6 g (0.166 mol) of methyl iodide are added dropwise, and the reaction mixture is warmed to a temperature of 22CC. After a further 2 hours, the alumina is filtered off, the filtrate is added to water and the mixture is extracted with ethyl acetate. The ethyl acetate phase is washed with water and then with saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated. The residue is chromatographed over silica gel (mobile phase: ethyl-acetate/hexane 15/1). This gives 12.0 g (60% of theory) of 2-(bismethylsulfanylmethylene)-1-cyciopropyl-3-(2-methyl-6-trifluoromethylpyridin-3-yl)-propane-1,3-dione as a solid. 12.0 g (0.033 mol) of the product obtained above are, together with 5.4 g (0.066 mol) of anhydrous sodium acetate, suspended in 120 ml of ethanol. 4.6 g (0.066 mol) of hydroxylarrune hydrochloride are added, and the reaction mixture is kept at a temp.erature of 22°C for 5 hours. Another 2.7 g of anhydrous sodium acetate and 2.3 g of hydroxylamine hydrochloride are then added. After 18 hours, the reaction mixture is diluted with water and extracted with ethyl acetate. The ethyl acetate phase is washed with water and then with saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated. Trituration with a little ethyl acetate gives 9.0 g (79.5%) of the desired product as a 2:1 isomer mixture in the form of white crystals (m.p. 103-104°C). Main isomer: 1H NMR (CDCI3, ppm) ((5-cyclopropyl-3-methylsulfanylisoxazol-4-yl)-(2-methyl-6-trifluoromethylpyridin-3-yl)methanone) 7.98, d, J=7.8 Hz, 1H; 7.61, d, J=7.8 Hz, 1H; 2.67, s, 3H; 2.50, s, 3H; 2.02-1.93, m, 1H; 1.34-1.28, m, 2H; 1.18-1.09, m, 2H. 1H NMR (CDCI3, ppm) (cyclopropyl-[3-methylsulfanyl-5-(2-methyl-6-trifluoromethylpyridin-3-yl)isoxazol-4-yl]methane): 7.95, d, J=7.8 Hz, 1H; 7.69, d, J=7.8 Hz, 1H; 2.67, s, 3H; 2.66, s, 3H; 1.74-1.64, m, 1H; 1.28-1.18, m, 2H; 0.89-0.80, m, 2H. Example H26: Preparation of (5-cvclopropyl-3-methvlsulfinvlisoxazol-4-vl)-(2-methvl-6-trifluoromethvlpvridin-3-vl)methanone and cvclopropvl-[3-methanesulfinvl-5-(2-methvl-6-trifluoromethvlpvridin-3-vl)isoxazol-4-yllmethanone: 1.50 g (0.0043 mol) of the isomer mixture obtained above are dissolved in 30 ml of acetone/water (2:1 mixture), and 1.02 g (0.0048 mol) of sodium metaperiodate are added a little at a time at 22°C. After 5 hours, the reaction mixture is evaporated using a rotary evaporator. The residue is taken up in water and ethyl acetate. The ethyl acetate phase is dried over sodium sulfate and evaporated. The residue is chromatographed over silica gel (mobile phase: ethyl acetate/hexane 3/1). This gives initially 0.8 g (51% of theory) of (5-cyclopropyl-3-methylsulfinylisoxazol-4-yl)-(2-methyl-6-trifluoromethylpyridin-3-yl)methanone as white crystals (m.p. 96-97°C). 1H NMR (CDCI3, ppm): 7.86, d, J=7.8 Hz, 1H; 7.59, d, J=7.8 Hz, 1H; 3.078, s, 3H; 2.66, s, 3H; 1.54-1.49, m, 1H; 1.32-1.25, m, 2H; 1.13-1.072, m, 2H. The second product that elutes consists of 0.34 g (22% of theory) of cyclopropyl-[3-methanesulfinyl-5-(2-methyl-6-trifluoromethyipyridin-3-yl)isoxa2ol-4-yl]methanone as white crystals (m.p. 112-113°C). 1H NMR (CDCI3, ppm): 7.97, d, J=7.8 Hz, 1H; 7.67, d, J=7.8 Hz, 1H; 3.128, s, 3H; 2.62, s, 3H; 1.69-1.64, m, 1H; 1.26-1.18, m, 2H; 0.90-0.85, m, 2H. Example H27: Preparation of (5-cvclopropvl-3-methanesulfonvlisoxazol-4-vlH2-isopropvl-6-trifluoromethvlpyridin-3-vOmethanone: 0.15 g (0.0045 mol) of (5-cyclopropyl-3-methylsulfanyiisoxazol-4-yl)-(2-isopropyl-6-trifluoromethylpyridin-3-yl)methanone is dissolved in methylene chloride, and 0.28 ml of peracetic acid (39% in acetic acid, 0.0016 mol) are added dropwise at a temperature of 5°C. After 15 hours at 25°C, the reaction mixture is added to ethyl acetate and water, and the organic phase is washed with water, dried with sodium sulfate and evaporated. The residue is chromatographed over silica gel (mobile phase: ethyl acetate/hexane 5/1). This gives 0.121 g (74% of theory) of the expected product as white crystals (m.p.105-106°C). In an analogous manner, and according to the methods shown in the general reaction schemes 1-10 and in the references mentioned therein, it is also possible to prepare the compounds listed in the tables below. In these tables, CCH is the ethynyl group, Ph is the phenyl group and Me is the methyl group. Comp. R1 R2 Ra R4 R5 P No. " 1.001 H CF3 H H OH 0 1.2 F CF3 H H OH 0 1.3 CI CF3 H H OH 0 1.4 Br CF3 H H OH 0 1.005 - CHF2 CF3 H H OH 0 1.006 CCI3 CF3 H H OH 0 1.007 CCIF2 CF3 H H OH 0 1.8 CF3 CF3 H H OH 0 1.9 CH3 CF3 H H OH 0 1.01 CH2CH3 CF3 H H OH 0 1.11 CH(CH3)2 CF3 H H OH 0 1.12 (CH2)2CH3 CF3 H H OH 0 1.013 C(CH3)3 CF3 H H OH 0 1.014 Ph CF3 H H OH 0 1.15 CH2F CF3 H H OH 0 1.16 CH2CI CF3 H H OH 0 1.17 CH2Br CF3 H H OH 0 1.18 CH2OH CF3 H H OH 0 1.019 CH2OCOCH3 CF3 H H OH 0 1.02 CH2OCOPh CF3 H H OH 0 1.021 CH2OCH3 CF3 H H OH 0 1.22 CH2OCH2CH3 CF3 H H OH 0 1.23 CH2CH2OCH3 CF3 H H OH 0 1.024 CH2SMe CF3 H H OH 0 1.25 CH2SOMe CF3 H H OH 0 1.26 CH2S02Me CF3 H H OH 0 1.27 CH2S02Ph CF3 H H OH 0 1.028 SCH2Ph CF3 H H : OH 0 1.029 SOCH2Ph CF3 H H OH 0 1.03 S02CH2Ph CF3 H H OH 0 1.031 SCH3 CF3 H H OH ' 0 Comp. R1 R2 R3 R4 R5 P No. 1.32 SOCH3 CF3 H H OH 0 1.33 S02CH3 CF3 H H OH 0 1.034 SPh CF3 H H OH 0 1.35 SOPh CF3 H H OH 0 1.36 S02Ph CF3 H H OH 0 1.37 N(CH3)2 CF3 H H OH 0 1.38 CH=CH2 CF3 H H OH 0 1.039 CH2CH=CH2 CF3 H H OH 0 1.04 S02N(CH3)2 CF3 H H OH 0 1.041 ethynyl CF3 H H OH 0 1.042 cyclopropyl CF3 H H OH 0 1.43 OCH3 CF3 H H OH 0 1.44 OPh CF3 H H OH 0 1.45 OCHF2 CF3 H H OH 0 1.46 C02Me CF3 H H OH 0 1.47 2-furyl CF3 H H OH 0 1.048 OCH2ethynyl CF3 H H OH 0 1.049 2-pyridyl CF3 H H OH 0 1.05 3-pyridyl CF3 H H OH 0 1.051 4-pyridyl CF3 H H OH 0 1.52 H CF3 H H OH 1 1.53 F CF3 H H OH 1 1.54 CI CF3 H H OH 1 1.55 Br CF3 H H OH 1 1.56 CHF2 CF3 H H OH 1 1.57 CCI3 CF3 H H OH 1 1.58 CCIF2 CF3 H H OH 1 1.059 CF3 CF3 H H 1.06 CH3 CF3 H H OH 1 1.061 CH2CH3 CF3 H H OH 1 1.062 CH(CH3)2 CF3 H H OH ' 1 Comp. R1 R2 R3 R4 R5 P No. 1.063 (CH2)2CH3 CF3 H H OH - 1 1.064 C(CH3)3 CF3 H H OH 1 1.065 Ph CF3 H H OH 1 1.66 CH2F CF3 H H OH 1 1.67 CH2CI CF3 H H OH 1 1.68 CH2Br CF3 H H OH 1 1.069 CH2OH CF3 H H OH 1 1.07 CH2OCOCH3 CF3 H H OH 1 1.071 CH2OCOPh CF3 H H OH 1 1.072 CH2OCH3 CF3 H H OH 1 1.73 CH2OCH2CH3 CF3 H H OH 1 1.74 CH2CH2OCH3 CF3 H H OH 1 1.075 CH2SMe CF3 H H OH 1 1.76 CH2SOMe CF3 H H OH 1 1.77 CH2S02Me CF3 H H OH 1 1.78 CH2S02Ph CF3 H H OH 1 1.079 SCH2Ph CF3 H H OH 1 1.08 SOCH2Ph CF3 H H OH 1 1.081 S02CH2Ph CF3 H H OH 1 1.082 SCH3 CF3 H H OH 1 1.83 SOCH3 CF3 H H OH 1 1.84 S02CH3 CF3 H H OH 1 1.085 SPh CF3 H H OH 1 1.86 SOPh CF3 H H OH 1 1.87 S02Ph CF3 H H OH 1 1.88 N(CH3)2 CF3 H H OH 1 1.89 CH=CH2 CF3 H H OH 1 1.09 CH2CH=CH2 CF3 H H 1.091 S02N(CH3)2 CF3 H H OH 1 1.092 ethynyl CF3 H H OH 1 1.093 cyclopropyl CF3 H H OH ' 1 Comp. R1 R2 R3 R4 R5 P No. 1.094 OCH3 CF3 "H H OH 1 1.095 OPh CF3 H H OH 1 ' 1.96 OCHF2 CF3 H H OH 1 1.97 C02Me CF3 H H OH 1 1.98 2-furyl CF3 H H OH 1 1.099 OCH2CCH CF3 H H OH 1 1.1 2-pyridyl CF3 H H OH 1 1.101 3-pyridyl CF3 H H OH 1 1.102 4-pyridyl CF3 H H OH 1 1.103 H CF2CF3 H H OH 0 1.104 CI CF2CF3 H H OH 0 1.105 CHF2 CF2CF3 H H OH 0 1.106 CCI3 CF2CF3 H H OH 0 1.107 CCIF2 CF2CF3 H H OH 0 1.108 CF3 CF2CF3 H H OH 0 1.109 CH3 CF2CF3 H H OH 0 1.11 CH2CH3 CF2CF3 • H H OH 0 1.111 CH(CH3)2 CF2CF3 H H OH 0 1.112 (CH2)2CH3 CF2CF3 H H OH 0 1.113 C(CH3)3 CF2CF3 H H OH 0 1.114 CH2F CF2CF3 H H OH 0 1.115 CH2CI CF2CF3 H H OH 0 1.116 CH2OH CF2CF3 H H OH 0 1.117 CH2OCOCH3 CF2CF3 H H OH 0 1.118 CH2OCOPh CF2CF3 H H OH 0 1.119 CH2OCH3 CF2CF3 H H OH 0 1.12 CH2OCH2CH3 CF2CF3 H . H OH 0 1.121 CH2SMe CF2CF3 H H 1.122 CH2SOMe CF2CF3 H H OH 0 1.123 CH2S02Me CF2CF3 H H OH 0 1.124 CH2S02Ph CF2CF3 H H OH ' 0 Comp. R1 R2 R3 R4 R5 P No. 1.125 N(CH3)2 CF2CF3 H H OH 0 1.126 CH=CH2 CF2CF3 H H OH 0 ' 1.127 CH2CH=CH2 CF2CF3 H H OH 0 1.128 S02N(CH3)2 CF2CF3 H H OH 0 1.129 CCH CF2CF3 H H OH 0 1.13 cyclopropyl CF2CF3 H H OH 0 1.131 OPh CF2CF3 H H OH 0 1.132 OCH3 CF2CF3 H H OH 0 1.133 C02Me CF2CF3 H H OH 0 1.134 OCH2CCH CF2CF3 H H OH 0 1.135 2-pyridyl CF2CF3 H H OH 0 1.136 3-pyridyl CF2CF3 H H OH 0 1.137 4-pyridyi CF2CF3 H H OH 0 1.138 H CF2CF3 H H OH 1 1.139 CI CF2CF3 H H OH 1 1.14 CHF2 CF2CF3 H H OH 1 1.141 CCI3 CF2CF3 H H OH 1 1.142 CCIF2 CF2CF3 H H OH 1 1.143 CF3 CF2CF3 H H OH 1 1.144 CH3 CF2CF3 H H OH 1 1.145 CH2CH3 CF2CF3 H H OH 1 1.146 CH(CH3)2 CF2CF3 H H OH 1 1.147 (CH2)2CH3 CF2CF3 H H OH 1 1.148 C(CH3)3 CF2CF3 H H OH 1 1.149 CH2F CF2CF3 H H OH 1 1.15 CH2CI CF2CF3 H H OH 1 1.151 CH2OH CF2CF3 H H OH -1 1.152 CH2OCOCH3 CF2CF3 H H -, OH 1 1.153 CH2OCOPh CF2CF3 H H OH 1 1.154 CH2OCH3 CF2CF3 H H OH 1 1.155 CH2OCH2CH3 CF2CF3 H H OH ' 1 Comp. R1 R2 R3 R4 R5 P No. 1.156 CH2SMe CF2CF3 H H OH 1 1.157 CH2SOMe CF2CF3 H H OH 1 1.158 CH2S02Me CF2CF3 H H OH 1 1.159 CH2S02Ph CF2CF3 H H OH 1 1.16 N(CH3)2 CF2CF3 H H OH 1 1.161 CH=CH2 CF2CF3 H H OH 1 1.162 CH2CH=CH2 CF2CF3 H H OH 1 1.163 S02N(CH3)2 CF2CF3 H H OH 1 1.164 CCH CF2CF3 H H OH 1 1.165 cyctopropyl CF2CF3 H H OH 1 1.166 OPh CF2CF3 H H OH 1 1.167 OCH3 CF2CF3 H H OH 1 1.168 C02Me CF2CF3 H H OH 1 1.169 OCH2CCH CF2CF3 H H OH 1 1.17 2-pyridyi CF2CF3 H H OH 1 1.171 3-pyridyl CF2CF3 H H OH 1 1.172 4-pyridyl CF2CF3 H H OH 1 1.173 H CF2CF2CF3 H H OH 0 1.174 CHF2 CF2CF2CF3 H H OH 0 1.175 CF3 CF2CF2CF3 H H OH 0 1.176 CH3 CF2CF2CF3 H H OH 0 1.177 CH2CH3 CF2CF2CF3 H H OH 0 1.178 (CH2)2CH3 CF2CF2CF3 H H OH 0 1.179 CH2CI CF2CF2CF3 H H OH 0 1.18 CH2OCH3 CF2CF2CF3 H H OH 0 1.181 H CF2CF2CF3 H H OH 1 1.182 CHF2 CF2CF2CF3 H H OH 1 1.183 CF3 CF2CF2CF3 H H .. OH 1 1.184 CH3 CF2CF2CF3 H H OH 1 1.185 CH2CH3 CF2CF2CF3 H H OH 1 1.186 (CH2)2CH3 CF2CF2CF3 H H OH ' 0 Comp. R1 R2 R3 R4 R5 P No. 1.187 CH2CI CF2CF2CF3 H H OH 1 1.188 CH2OCH3 CF2CF2CF3 H H OH 1 1.189 H CF2CI H H OH 0 1.19 CI CF2CI H H OH 0 1.191 CHF2 CF2CI H H OH 0 1.192 CCI3 CF2CI H H OH 0 1.193 CCIF2 CF2CI H H OH 0 1.194 CF3 CF2CI H H OH 0 1.195 CH3 CF2CI H H OH 0 1.196 CH2CH3 CF2CI H H OH 0 1.197 CH(CH3)2 CF2CI H H OH 0 1.198 (CH2)2CH3 CF2CI H H OH 0 1.199 C(CH3)3 CF2CI H H OH 0 1.2 CH2F CF2CI H H OH 0 1.201 CH2CI CF2CI H H OH 0 1.202 CH2OH CF2CI H H OH 0 1.203 CH2OCOCH3 CF2CI H H OH 0 1.204 CH2OCOPh CF2CI H H OH 0 1.205 CH2OCH3 CF2CI H H OH 0 1.206 CH2OCH2CH3 CF2CI H H OH 0 1.207 CH2SMe CF2CI H H OH 0 1.208 CH2SOMe CF2CI H H OH 0 1.209 CH2S02Me CF2CI H H OH 0 1.21 CH2S02Ph. CF2CI H H OH 0 1.211 N(CH3)2 CF2CI H H OH 0 1.212 CH=CH2 CF2CI H H OH 0 1.213 CH2CH=CH2 CF2CI H H OH 0 1.214 S02N(CH3)2 CF2CI H H <. oh> 1.215 CCH CF2CI H H OH 0 1.216 cyclopropyl CF2CI H H OH 0 1.217 OPh CF2CI H H OH ' 0 Comp. R1 R2 R3 R4 R5 P No. 1.218 OCH3 CF2CI H H OH 0 1.219 C02Me CF2CI H H OH 0 1.22 OCH2CCH CF2CI H H OH 0 1.221 2-pyridyf CFjCI H H OH 0 1.222 3-pyridyl CF2CI H H OH 0 1.223 4-pyridyl CF2CI H H OH 0 1.224 H CF2CI H H OH 1 1.225 CI CF2CI H H OH 1 1.226 CHF2 CF2CI H H OH 1 1.227 CCI3 CF2CI H H OH 1 1.228 CCIF2 CF2CI H H OH 1 1.229 CF3 CF2CI H H OH 1 1.23 CH3 CF2CI H H OH 1 1.231 CH2CH3 CF2CI H H OH 1 1.232 CH(CH3)2 CF2CI H H OH 1 1.233 (CH2)2CH3 CF2CI H H OH 1 1.234 C(CH3)3 CF2CI H H OH 1 1.235 CH2F CF2CI H H OH 1 1.236 CH2CI CF2CI H H OH 1 1.237 CH2OH CF2CI H H OH 1 1.238 CH2OCOCH3 CF2CI H H OH 1 1.239 CH2OCOPh CF2CI H H OH 1 1.24 CH2OCH3 CF2CI H H OH 1 1.241 CH2OCH2CH3 CF2CI H H OH 1 1.242 CH2SMe CF2CI H H OH 1 1.243 CH2SOMe CF2CI H H OH 1 1.244 CH2S02Me CF2CI H H OH 1 1.245 CH2S02Ph CF2CI H H -, OH 1 1.246 N(CH3)2 CF2CI H H OH 1 1.247 CH=CH2 CF2CI H H OH 1 1.248 CH2CH=CH2 CF2CI H H OH 1 Comp. R1 R2 R3 R4 R5 p No. 1.249 S02N(CH3)2 ■ CF2Ci H H OH 1 1.25 CCH CF2CI H H OH 1 1.251 cyclopropyl CF2CI H H OH 1 1.252 OPh CF2CI H H OH 1 1.253 OCH3 CF2CI H H OH 1 1.254 C02Me CF2CI H H OH 1 1.255 OCH2CCH CF2CI H H OH 1 1.256 H CCI3 H H OH 0 1.257 CI CCI3 H H OH 0 1.258 CH3 CCI3 H H OH 0 1.259 CH2CH3 CCI3 H H OH 0 1.26 CH(CH3)2 CCI3 H H OH 0 1.261 (CH2)2CH3 CCI3 H H OH 0 1.262 CH2F CCI3 H H OH 0 1.263 CH2CI CCI3 H H OH 0 1.264 CH2OH CCI3 H H OH 0 1.265 CH2OCOCH3 CCI3 H H OH 0 1.266 CH2OCOPh CCI3 H H OH 0 1.267 CH2OCH3 CCI3 H H OH 0 1.268 CH2OCH2CH3 CCI3 H H OH 0 1.269 CH2SMe CCI3 H H OH 0 1.27 CH2SOMe CCI3 H H OH 0 1.271 CH2S02Me CCI3 H ' H OH 0 1.272 CH2S02Ph CCI3 H H OH 0 1.273 cyclopropyl CCI3 H H OH 0 1.274 OPh CCI3 H H OH 0 1.275 OCH3 CCI3 H H OH 0 1.276 C02Me CCI3 H H «, OH 0 1.277 OCH2CCH CCI3 H H OH 0 1.278 H CCI3 H H OH 1 1.279 CI CCI3 H H OH ' 1 Comp. R1 R2 R3 R4 Rs P No. 1.28 CH3 CCI3 H H OH 1 1.281 CH2CH3 CCI3 H H OH 1 ' 1.282 CH(CH3)2 CCb H H OH 1 1.283 (CH2)2CH3 CCb H H OH 1 1.284 CH2F CCI3 H H OH 1 1.285 CH2CI CCI3 H H OH 1 1.286 CH2OH CCI3 H H OH 1 1.287 CH2OCOCH3 CCI3 H H OH 1 1.288 CH2OCOP.h CCI3 H H OH 1 1.289 CH2OCH3 CCI3 H H OH 1 1.29 CH2OCH2CH3 CCI3 H H OH 1 1.291 CH2SMe CCI3 H H OH 1 1.292 CH2SOMe CCI3 H H OH 1 1.293 CH2S02Me CCI3 H H OH 1 1.294 CH2S02Ph CCI3 H H OH 1 1.295 cyclopropyl CCI3 H H OH 1 1.296 OPh CCI3 H H OH 1 1.297 OCH3 CCI3 H H OH 1 1.298 C02Me CCI3 H H OH 1 1.299 OCH2CCH CCI3 H H OH 1 1.3 CF3 CHF2 H H OH 0 1.301 CH3 CHF2 H H OH 0 1.302 CH2OCH3 CHF2 H H OH 0 1.303 CH2CI CHF2 H H OH 0 1.304 CH2F CHF2 H H OH 0 1.305 CF3 CHF2 H H OH 1 1.306 CH3 CHF2 H H OH 1 1.307 CH2OCH3 CHF2 H H j OH 1 1.308 CH2CI CHF2 H H OH 1 1.309 CH2F CHF2 H H OH 1 1.31 CH3 CF3 H CH3 OH ' 0 Comp. R1 R2 R3 R4 R5 P No. 1.311 CH3 CF3 H CH3 OH 1 1.312 CI CF3 H CH3 OH 0 1.313 CH3 CF3 CH3 H OH 0 1.314 CH3 CF3 Ph H OH 0 1.315 CH3 CF3 CI H OH 0 1.316 CH3 CF3 C02CH2CH3 H OH 0 1.317 CH3 CF3 C02CH2Ph H OH 0 1.318 CH3 CF3 CH3 H OH 1 1.319 CH3 CF3 Ph H OH 1 1.32 CH3 CF3 CI H OH 1 1.321 CH3 CF3 C02CH2CH3 H OH 1 1.322 CH3 CF3 C02CH2Ph H OH 1 1.323 OCH3 CF3 CH3 H OH 0 1.324 CH2OCH3 CF3 CH3 H OH 0 1.325 CH2OCH3 CF3 Ph H OH 0 1.326 CH2OCH3 CF3 CI H OH 0 1.327 CH2OCH3 CF3 C02CH2CH3 H OH 0 1.328 CH2OCH3 CF3 C02CH2Ph H OH 0 1.329 CH2OCH3 CF3 CH3 H OH 1 1.33 CH2OCH3 CF3 Ph H OH 1 1.331 CH2OCH3 CF3 CI H OH 1 1.332 CH2OCH3 CF3 C02CH2CH3 H OH 1 1.333 CH2OCH3 CF3 C02CH2Ph H OH 1 1.334 COOCH3 H H H OH 0 1.335 CF3 SCH3 H H OH 0 1.336 CH3 SCH3 H H OH 0 1.337 CF3 SOCH3 H H OH 0 1.338 CH3 SOCH3 H H -.OH 0 1.339 CF3 S02CH3 H H OH 0 1.34 CH3 S02CH3 H H OH 0 1.341 CF3 SCH2CH3 H H OH ' 0 Comp. R, R2 R3 R4 Rs p No. 1.342 CH3 SCH2CH3 H H OH 0 1.343 CF3 SOCH2CH3 H H OH 0 1.344 CH3 SOCH2CH3 H H OH 0 1.345 CF3 S02CH2CH3 H H OH 0 1.346 CH3 S02CH2CH3 H H OH 0 1.347 CF3 OCH3 H H OH 0 1.348 CH3 OCH3 H H OH 0 1.349 CF3 OCH2CF3 H H OH 0 1-35 CH3 OCH2CF3 H H OH 0 1.351 CF3 OCH2CCH H H OH 0 1.352 CH3 OCH2CCH H H OH 0 1.353 CF3 CN H H OH 0 1.354 CH3 CN H H OH 0 1.355 CF3 CI H H OH 0 1-356 CF3 CI H H 0-NEt3+ 0 1.357 CH3 CI H H OH 0 1-358 H CI H H OH 0 1.359 CF3 OCH3 H H OH 0 1.36 CH3 OCH3 H H OH 0 1-361 CF3 CH3 H H OH 0 1-362 H CF3 H CH3 OH 0 1-363 H CF3 H CF3 OH 0 1-364 H CF3 H CH2CH3 OH 0 1-365 H CF3 H CF3 OH 0 1-366- H CF3 H SCH3 OH 0 1-367 H CF3 H SOCH3 OH 0 1-368 H CF3 H S02CH3 OH 0 1-369 H CF3 H CI ,, OH 0 1-37 H CF3 H OCH3 OH 0 1-371 H CH3 H CF3 OH t 0 1-372 H CI H CF3 OH 0 Comp. R1 R2 R3 R4 R5 P No. 1.373 H OCH3 H CF3 OH 0 1.374 H SCH3 H CF3 OH 0 1.375 H SOCH3 H CF3 OH 0 1.376 CH3 CF3 H H O-K+ 0 1.377 CH3 CF3 H H S(CH2)7CH3 0 1.378 CH3 CF3 H H S(CH2)7CH3 0 1.379 CH3 CF3 H H SO(CH2)7CH3 0 1.38 CH3 CF3 H H S02(CH2)7CH3 0 1.381 CH3 CF3 H H SPh 0 1.382 CH3 CF3 H H SOPh 0 1.383 CH3 CF3 H H S02Ph 0 1.384 CH3 CF3 H H NOCH3 0 1.385 CH3 CF3 H H NOCH2Ph 0 1.386 CH3 CF3 H H NOCH2CH=CH2 0 1.387 CH3 CF3 H H NOC(CH3)3 0 1.388 CH3 CF3 H H NOCH2CH3 0 1.389 CH3 CF3 H H NCH2CH2SH 0 1.39 CH3 CF3 H H NN(CH3)2 0 1.391 CH3 CF3 H H NN(CH3)C(S)NH2 0 1.392 CH3 CF3 H H N-morpholino 0 1.393 CH3 CF3 H H NHCOCH3 0 1.394 CH3 CF3 H H NHCO(CH2)7CH3 0 \395 CH3 CF3 H H NHCOPh 0 1.396 CH3 CF3 H H NHS02CH3 0 1.397 CH3 CF3 H H NH(C0)S(CH2)7CH3 0 1.398 CH3 CF3 H H CI 0 1.399 CH3 CF3 H H NH2 0 1.4 CH3 CF3 H H OCOC(CH3)3 0 1.401 CH3 CF3 H H OCOCH3 0 1.402 CH3 CF3 H H OCOPh 0 1.403 CH3 CF3 H H OCO-cyclopropyl 0 Comp. R1 R2 R3 R4 R5 P No. - 1.404 CH3 CF3 H H OCOC"H2CH3 0 1.405 CH3 CF3 H H OCOCH=CH2 0 1.406 CH3 CF3 H H OCOCH=CHCH3 0 1.407 CH3 CF3 H H 0(CO)SCH3 0 1.408 CH3 CF3 H H 0(CO)S(CH2)7CH3 0 1.409 CH3 CF3 H H 0(CO)OCH2CH3 0 1.41 CH3 CF3 H H 0(CO)N(CH2CH3)2 0 1.411 CH3 (CF2)3CF3 H H OH 0 1.412 CH3 CF3 H H S-(4-CI-phenyl) 0 1.413 CH3 CF3 H H SO-(4-CI-phenyl) 0 1.414 CH3 CF3 H H S02-(4-CI-phenyl) 0 1.415 CH3 CF3 H H S-(4-CF3-phenyl) 0 1.416 CH3 CF3 H H SO-(4-CF3-phenyl) 0 1.417 CH3 CF3 H H S02-(4-CF3-phenyl) 0 1.418 CH3 CF3 H H S-(4-N02-phenyl) 0 1.419 CH3 CF3 H H SO-(4-N02-phenyl) 0 1.42 CH3 CF3 H H SOr(4-N02-phenyl) 0 1.425 CF2H SCH3 H H OH 0 1.426 CF2CI SCH3 H H OH 0 1.427 CF2H SOCH3 H H OH 0 1.428 CF2CI SOCH3 H H OH 0 1.429 CF2H S02CH3 H H OH 0 1.43 CF2CI S02CH3 H H OH 0 Comp. R1 R2 R3 R4 R5 P No. 1.431 CF2H SCH2CH3 H H OH 0 1.432 CF2CI SCH2CH3 H H OH 0 ' 1.433 CF2H SOCH2CH3 H H OH 0 1.434 CF2CI SOCH2CH3 H H OH 0 1.435 CF2H SO2CH2CH3 H H OH 0 1.436 CF2CI SO2CH2CH3 H H OH 0 1.437 CF2H OCH3 H H OH 0 1.438 CF2CI OCH3 H H OH 0 1.439 CF2H OCH2CF3 H H OH 0 1.44 CF2CI OCH2CF3 H H OH 0 1.441 CF2H OCH2CCH H H OH 0 1.442 CF2C! OCH2CCH H H OH 0 1.443 CF2H CN H H OH 0 1.444 CF2CI CN H H OH 0 1.445 CF2H CI H H OH 0 1.446 CF2CI CI H H OH 0 1.447 CF2H OCH3 H H OH 0 1.448 CF2CI OCH3 H H OH 0 1.449 CF3 CH2OCH3 H H OH 0 1.45 CF3 CH2OCH3 H H OH 1 1.451 CF2CI CH2OCH3 H H OH 0 1.452 CF2CI CH2OCH3 H H OH 1 1.453 CF2H CH2OCH3 H H OH 0 1.454 CF2H CH2OCH3 H H OH 1 1.455 CN CF3 H H OH 0 Table 2: 2.1 H CF3 H H 2.2 F CF3 H H 2.3 CI CF3 H H 2.4 Br CF3 H H 2.5 CHF2 CF3 H H 2.6 CCI3 CF3 H H 2.007 CCIF2 CF3 H H 2.8 CF3 CF3 H H 2.9 CH3 CF3 H H 2.01 CH2CH3 CF3 H H 2.11 CH(CH3)2 CF3 H H 2.12 (CH2)2CH3 CF3 H H 2.013 Ph CF3 H H 2.14 CH2F CF3 H H 2.15 CH2CI CF3 H H 2.16 CH2Br CF3 H H 2.17 CH2OH CF3 H H 2.018 CH2OCOCH3 CF3 H H 2.019 CH2OCOPh CF3 H H 2.02 CH2OCH3 CF3 H H 2.021 CH2OCH2CH3 CF3 H H 2.022 CH2CH2OCH3 CF3 H H 2.023 CH2SMe CF3 H H ' 2.024 CH2SOMe CF3 H H 2.025 CH2S02Me CF3 H H 2.026 CH2S02Ph CF3 H H Comp. No. R, R2 R3 R1 2.027 SCH2Ph CF3 H H 2.28 SOCH2Ph CF3 H H 2.29 S02CH2Ph CF3 H H 2.03 SCH3 CF3 H H 2.31 SOCH3 CF3 H H 2.32 S02CH3 CF3 H H 2.33 N(CH3)2 CF3 H H 2.34 CH=CH2 CF3 H H 2.35 CH2CH=CH2 CF3 H H 2.36 S02N(CH3)2 CF3 H ' H 2.37 CCH CF3 H H 2.38 OCH3 CF3 H H 2.039 OPh CF3 H H 2.04 OCHF2 CF3 H H 2.041 C02Me CF3 H H 2.42 OCH2CCH CF3 H H 2.43 OCH2CF3 CF3 H H 2.046 CN CF3 H H 2.047 H CHF2 H H 2.048 CH3 CHF2 H H 2.049 CH2CH3 CHF2 H H 2.05 CH2OCH3 CHF2 H H 2.051 H CF2CI H H 2.052 CH3 CF2CI H H 2.053 CH2CH3 CF2CI H H 2.054 CH2OCH3 CF2CI H H Table 3: Comp. No. R1 R2 R3 Ft, 3.1 H CF3 H H 3.2 F CF3 H H 3.3 CI CF3 H H 3.4 Br CF3 H H 3.5 CHF2 CF3 H H 3.6 CCI3 CF3 H H 3.7 CCIF2 CF3 H H 3.8 CF3 CF3 H H 3.9 CH3 CF3 H H 3.01 CH2CH3 CF3 H H 3.11 CH(CH3)2 CF3 H H 3.12 (CH2)2CH3 CF3 H H 3.013 Ph CF3 H H 3.14 CH2F CF3 H H 3.15 CH2CI CF3 H H 3.16 CH2Br CF3 H H 3.17 CH2OH CF3 H H 3.018 CH2OCOCH3 CF3 H H 3.019 CH2OCQPh CF3 H . H 3.02 CH2OCH3 CF3 H H 3.21 CH2OCH2CH3 CF3 H H 3.22 CH2CH2OCH3 CF3 H H 3.023 CH2SMe CF3 H H 3.24 CH2SOMe CF3 H H 3.25 CH2S02Me CF3 H H Comp. No. R, R2 R3 FU 3.026 CH2SOzPh CF3 H H • 3.027 SCH2Ph CF3 H H 3.28 SOCH2Ph CF3 H H 3.29 S02CH2Ph CF3 H H 3.03 SCH3 CF3 H H 3.31 SOCH3 CF3 H H 3.32 S02CH3 CF3 H H 3.33 N(CH3)2 CF3 H H 3.34 CH=CH2 CF3 H H 3.35 CH2CH=CH2 CF3 H H 3.36 S02N(CH3)2 CF3 H H 3.37 CCH CF3 H H 3.38 OCH3 CF3 H H 3.039 OPh CF3 H H 3.04 OCHF2 CF3 H H 3.041 C02Me CF3 H H 3.42 OCH2CCH CF3 H H 3.43 OCH2CF3 CF3 H H 3.044 H CF3 H H 3.045 CN CF3 H H 3.046 H CHF2 H H 3.047 CH3 CHF2 H H 3.048 CH2CH3 CHF2 H H 3.049 CH2OCH3 CHF2 H H 3.05 H CF2CI H H 3.051 CH3 CF2CI H H 3.052 CH2CH3 CF2CI H H 3.053 CH2OCH3 CF2CI H H 3.54 CI CH3 H H 3.55 CN SCH3 H H 3.56 CN S02CH3 H H Table 4: Comp. R, R2 R3 R4 R5 P No. 4.1 H CF3 H H OH 0 4.2 F CF3 H H OH 0 4.3 CI CF3 H H OH 0 4.4 Br CF3 H H OH 0 4.5 CHF2 CF3 H H OH 0 4.6 CCI3 CF3 H H OH 0 4.7 CCIF2 CF3 H H OH 0 4.8 CF3 CF3 H H OH 0 4.9 CH3 CF3 H H OH 0 4.01 CH2CH3 CF3 H H OH 0 4.11 CH(CH3)2 CF3 H H OH 0 4.12 (CH2)2CH3 CF3 H H OH 0 4.013 C(CH3)3 CF3 H H OH 0 4.014 Ph CF3 H H OH 0 4.15 CH2F CF3 H H OH 0 4.16 CH2CI CF3 H H OH 0 4.17 CH2Br CF3 H H OH. 0 ■ . 4.018 CH2OH CF3 H H OH 0 4.019 CH2OCOCH3 CF3 H H OH 0 4.02 CH2OCOPh CF3 H H 'OH 0 4.021 CH2OCH3 CF3 H H OH 0 4.22 CH2OCH2CH3 CF3 H H OH , 0 4.23 CH2CH2OCH3 CF3 H H OH 0 Comp. R1 R2 R3 R4 R5 P No. 4.024 CH2SMe CF3 H H OH 0 4.25 CH2SOMe CF3 H H OH 0 4.26 CH2S02Me CF3 H H OH 0 4.27 CH2S02Ph CF3 H H OH 0 4.28 N(CH3)2 CF3 H H OH 0 4.29 CH=CH2 CF3 H H OH 0 4.03 CH2CH=CH2 CF3 H H OH 0 4.031 S02N(CH3)2 CF3 H H OH 0 4.032 CCH CF3 H H OH 0 4.033 cyclopropyl CF3 H H OH 0 4.034 OCH3 CF3 H H OH 0 4.035 OPh CF3 H H OH 0 4.36 OCHF2 CF3 H H OH 0 4.37 C02Me CF3 H H OH 0 4.038 OCH2CCH CF3 H H OH 0 4.039 H CF3 H H OH 1 4.04 F CF3 H H OH 1 4.41 CI CF3 H H OH 1 4.42 Br CF3 H H OH 1 4.43 CHF2 CF3 H H OH 1 4.44 CCI3 CF3 H H OH 1 4.45 CCIF2 CF3 H H OH 1 4.46 CF3 CF3 H ' H OH 1 4.47 CH3 CF3 H H OH 1 4.048 CH2CH3 CF3 H H OH 1 4.049 CH(CH3)2 CF3 H H OH 1 4.05 (CH2)2CH3 CF3 H H OH 1 4.051 C(CH3)3 CF3 H H ..OH 1 4.052 Ph CF3 H H OH 1 4.53 CH2F CF3 H H OH 1 4.54 CH2CI CF3 H H OH 1 Comp. R1 R2 R3 R4 R5 P No. 4.055 CH2Br CF3 H H OH 1 4.056 CH2OH CF3 H H OH 1 4.57 CH2OCOCH3 CF3 H H OH 1 4.58 CH2OCOPh CF3 H H OH 1 4.059 CH2OCH3 CF3 H H OH 1 4.06 CH2OCH2CH3 CF3 H H OH 1 4.061 CH2CH2OCH3 CF3 H H OH 1 4.062 CH2SMe CF3 H H OH 1 4.63 CH2SOMe CF3 H H OH 1 4.64 CH2S02Me CF3 H H OH 1 4.65 CH2S02Ph CF3 H H OH 1 4.66 N(CH3)2 CF3 H H OH 1 4.67 CH=CH2 CF3 H H OH 1 4.68 CH2CH=CH2 CF3 H H OH 1 4.69 S02N(CH3)2 CF3 H H OH 1 4.07 CCH CF3 H H OH 1 4.071 cyclopropyl CF3 H H OH 1 4.72 OCH3 CF3 H H OH 1 4.73 OPh CF3 H H OH 1 4.74 OCHF2 CF3 H H OH 1 4.75 C02Me CF3 H H OH 1 4.76 2-furyl CF3 H H OH 1 4.077 OCH2CCH CF3 H H OH 1 4.78 H CF2CF3 H H OH 0 4.79 CI CF2CF3 H H OH 0 t 4.08 CHF2 CF2CF3 H H OH 0 4.081 CCI3 CF2CF3 H H OH 0 4.082 CCIF2 CF2CF3 H H «, OH 0 4.83 CF3 CF2CF3 H H OH 0 4.84 CH3 CF2CF3 H H OH 0 4.085 CH2CH3 CF2CF3 H H OH ' 0 Comp. R1 R2 R3 R4 R5 P No. 4.86 CH(CH3)2 CF2CF3 H H OH 0 4.87 (CH2)2CH3 CF2CF3 H H OH 0 4.088 C(CH3)3 CF2CF3 H H OH 0 4.089 CH2F CF2CF3 H H OH 0 4.09 CH2CI CF2CF3 H H OH 0 4.091 CH2OH CF2CF3 H H OH 0 4.092 CH2OCOCH3 CF2CF3 H H OH 0 4.093 CH2OCOPh CF2CF3 H H OH 0 4.094 CH2OCH3 CF2CF3 H H OH 0 4.095 CH2OCH2CH3 CF2CF3 H H OH 0 4.096 CH2SMe CF2CF3 H H OH 0 4.97 CH2SOMe CF2CF3 H H OH 0 4.98 CH2S02Me CF2CF3 H H OH 0 4.99 CH2S02Ph CF2CF3 H H OH 0 4.1 N(CH3)2 CF2CF3 H H OH 0 4.101 CH=CH2 CF2CF3 H H OH 0 4.102 CH2CH=CH2 CF2CF3 H H OH 0 4.103 S02N(CH3)2 CF2CF3 H H OH 0 4.104 CCH CF2CF3 H H OH 0 4.105 cyclopropyl CF2CF3 H H OH 0 4.106 OPh CF2CF3 H H OH 0 4.107 OCH3 CF2CF3 H H OH 0 4.108 C02Me CF2CF3 H H OH 0 4.109 OCH2CCH CF2CF3 H H OH 0 4.11 H CF2CF2CF3 H H OH 0 t 4.111 CHF2 CF2CF2CF3 H H OH 0 4.112 CF3 CF2CF2CF3 H H OH 0 4.113 CH3 CF2CF2CF3 H H -.OH 0 4.114 CH2CH3 CF2CF2CF3 H H OH 0 4.115 (CH2)2CH3 CF2CF2CF3 H H OH 0 4.116 CH2CI CF2CF2CF3 H H OH ' 0 Comp. R1 R2 R3 R4 R5 P No. 4.117 CH2OCH3 CF2CF2CF3 H H OH 0 4.118 H CF2CI H H OH 0 4.119 CI CF2CI H H OH 0 4.12 CHF2 CF2CI H H OH 0 4.121 CCI3 CF2CI H H OH 0 4.122 CCIF2 CF2CI H H OH 0 4.123 CF3 CF2CI H H OH 0 4.124 CH3 CF2CI H H OH 0 4.125 CH2CH3 CF2CI H H OH 0 4.126 CH(CH3)2 CF2CI H H OH 0 4.127 (CH2)2CH3 CF2CI H H OH 0 4.128 C(CH3)3 CF2CI H H OH 0 4.129 CH2F CF2CI H H OH 0 4.13 CH2CI CF2CI H H OH 0 4.131 CH2OH CF2CI H H OH 0 4.132 CH2OCOCH3 CF2CI H H OH 0 4.133 CH2OCOPh CF2CI H H OH 0 4.134 CH2OCH3 CF2CI H H OH 0 4.135 CH2OCH2CH3 CF2CI H H OH 0 4.136 CH2SMe CF2CI H H OH 0 4.137 CH2SOMe CF2CI H H OH 0 4.138 CH2S02Me CF2CI H H OH 0 4.139 CH2SOzPh CF2CI H H OH 0 4.14 N(CH3)2 CF2CI H H OH 0 4.141 CH=CH2 CF2CI H H OH 0 4.142 CH2CH=CH2 CF2CI H H OH 0 4.143 S02N(CH3)2 CF2CI H H OH 0 4.144 CCH CF2CI H H •. OH 0 4.145 cyclopropyl CF2C! H H OH 0 4.146 OPh CF2CI H H OH 0 4.147 OCH3 CF2CI H H OH ' 0 Comp. R1 R2 R3 R4 R5 P No. 4.148 C02Me CF2CI • H H OH 0 4.149 OCH2CCH CF2CI H H OH 0 4.15 CH3 CF2CI H H OH 1 4.151 CH2OCH3 CF2CI H H OH 1 4.152 H CCI3 H H OH 0 4.153 CI CCI3 H H OH 0 4.154 CH3 CCI3 H H OH 0 4.155 CH2CH3 CCI3 H H OH 0 4.156 CH(CH3)2 CCI3 H H OH 0 4.157 (CH2)2CH3 CCI3 H H OH 0 4.158 CH2F CCI3 H H OH 0 4.159 CH2CI CCI3 H H OH 0 4.16 CH2OH CCI3 H H OH 0 4.161 CH2OCOCH3 CCI3 H H OH 0 4.162 CH2OCOPh CCI3 H H OH 0 4.163 CH2OCH3 CCI3 H H OH 0- 4.164 CH2OCH2CH3 CCI3 H H OH 0 4.165 CH2SMe CCI3 H H OH 0 4.166 CH2SOMe CCI3 H H OH 0 4.167 CH2S02Me CCI3 H H OH 0 4.168 CH2S02Ph CCI3 H H OH 0 4.169 cyclopropyl CCI3 H H OH 0 4.17 OPh CCI3 H H OH 0 4.171 OCH3 CCI3 H H OH 0 4.172 C02Me CCI3 H H OH 0 4.173 OCH2CCH " CCI3 H H OH 0 4.174 CF3 CHF2 H H OH 0 4.175 CH3 CHF2 H H '.OH 0 4.176 CH2OCH3 CHF2 H H OH 0 4.177 CH2CI CHF2 H H OH 0 4.178 CH2F CHF2 H H OH ' 0 Comp. R1 R2 R3 R4 R5 P No. 4.179 CF3 CHF2 H H OH 1 4.18 CH3 CHF2 H H OH 1 4.181 CH2OCH3 CHF2 H H OH 1 4.182 CH2CI CHF2 H H OH 1 4.183 CH2F CHF2 H H OH 1 4.184 CH3 CF3 H CH3 OH 0 4.185 CH3 CF3 H CH3 OH 1 4.186 CI CF3 H CH3 OH 0 4.187 CH3 CF3 CH3 H OH 0 4.188 CH3 CF3 Ph H OH 0 4.189 CH3 CF3 CI H OH 0 4.19 CH3 CF3 C02CH2CH3 H OH 0 4.191 CH3 CF3 C02CH2Ph H OH 0 4.192 CH3 CF3 CH3 H OH 1 4.193 CH3 CF3 Ph H OH 1 4.194 CH3 CF3 CI H OH 1 4.195 CH3 CF3 C02CH2CH3 H OH 1 4.196 CH3 CF3 C02CH2Ph H OH 1 4.197 OCH3 CF3 CH3 H OH 0 4.198 CH2OCH3 CF3 CH3 H OH 0 4.199 CH2OCH3 CF3 Ph H OH 0 4.2 CH2OCH3 CF3 CI H OH 0 4.201 CH2OCH3 CF3 C02CH2CH3 H OH 0 4.202 CH2OCH3 CF3 C02CH2Ph H OH 0 4.203 CH2OCH3 CF3 CH3 H OH 1 4.204 CH2OCH3 CF3 Ph H OH 1 4.205 CH2OCH3 CF3 CI H OH 1 4.206 CH2OCH3 CF3 C02CH2CH3 H ., OH 1 4.207 CH2OCH3 CF3 C02CH2Ph H OH 1 4.208 COOCH3 H H H OH 0 4.209 CF3 SCH3 H H OH ' 0 Comp. Hi R2 R3 R4 R5 P No. - 4.21 CH3 SCH3 H H OH 0 4.211 CF3 SOCH3 H H OH 0 4.212 CH3 SOCH3 H H OH 0 4.213 CF3 S02CH3 H H OH 0 4.214 CH3 S02CH3 H H OH 0 4.215 CF3 SCn2CH3 H H OH 0 4.216 CH3 SCn2CH3 H H OH 0 4.217 CF3 SOCH2CH3 H H OH 0 4.218 CH3 SOCH2CH3 H H OH 0 4.219 CF3 S02CH2CH3 H H OH 0 4.22 CH3 SO2CH2CH3 H H OH 0 4.221 CF3 OCH3 H H OH 0 4.222 CH3 OCH3 H H OH 0 4.223 CF3 OCH2CF3 H H OH 0 4.224 CH3 OCH2CF3 H H OH 0 4.225 CF3 OCH2CCH H H OH 0 4.226 CH3 OCH2CCH H H OH 0 4.227 CF3 CN H H OH 0 4.228 CH3 CN H H OH 0 4.229 CF3 CI H H OH 0 4.23 CH3 CI H H OH 0 4.231 H CI H H OH 0 4.232 CF3 OCH3 H H OH 0 4.233 CH3 OCH3 H H OH 0 4.234 CF3 CH3 H H OH 0 4.235 H CF3 H CH3 OH 0 4.236 H CF3 H CF3 OH 0 4.237 H CF3 H CH2CH3 «, OH 0 4.238 H CF3 H CF3 OH 0 4.239 H CF3 H SCH3 OH 0 4.24 H CF3 H SOCH3 OH 0 Comp. R, R2 R3 R4 R5 P No. 4.241 H CF3 H SO2CH3 OH 0 4.242 H CF3 H CI OH 0 4.243 H CF3 H OCH3 OH 0 4.244 H CH3 H CF3 OH 0 4.245 H CI H CF3 OH -0 4.246 H OCH3 H CF3 OH 0 4.247 H SCH3 H CF3 OH 0 4.248 H SOCH3 H CF3 OH 0 4.249 CH3 CF3 H H S(CH2)7CH3 0 4.25 CH3 CF3 H H S(CH2)7CH3 0 4.251 CH3 CF3 H H SO(CH2)7CH3 0 4.252 CH3 CF3 H H S02(CH2)7CH3 0 4.253 CH3 CF3 H H SPh 0 4.254 CH3 CF3 H H SOPh 0 4.255 CH3 CF3 H H S02Ph 0 4.256 CH3 CF3 H H NOCH3 0 4.257 CH3 CF3 H H NOCH2Ph 0 4.258 CH3 CF3 H H NOCH2CH=CH2 0 4.259 CH3 CF3 H H NOC(CH3)3 0 4.26 CH3 CF3 H H NOCH2CH3 0 4.261 CH3 CF3 H H NCH2CH2SH 0 4.262 CH3 CF3 H H NN(CH3)2 0 4.263 CH3 CF3 H H NN(CH3)C(S)NH2 0 4.264 CH3 CF3 H H N-morphoiino 0 4.265 CH3 CF3 H H NHCOCH3 0 t 4.266 CH3 CF3 H H NHCO(CH2)7CH3 0 4.267 CH3 CF3 H H NHCOPh 0 4.268 CH3 CF3 H H NHS02CH3 0 4.269 CH3 CF3 H H NH(CO)S(CH2)7CH3 0 4.27 CH3 CF3 H H CI 0 4.271 CH3 CF3 H H NH2 ' 0 Comp. R1 R2 R3 R4 R5 p No. 4.272 CH3 CF3 H H OCOC(CH3)3 0 4.273 CH3 CF3 H H OCOCH3 0 4.274 CH3 CF3 H H OCOPh 0 4.275 CH3 CF3 H H OCO-cyclopropyl 0 4.276 CH3 CF3 H H OCOCH2CH3 0 4.277 CH3 CF3 H H OCOCH=CH2 0 4.278 CH3 CF3 H H OCOCH=CHCH3 0 4.279 CH3 CF3 H H 0(CO)SCH3 0 4.28 CH3 CF3 H H 0(CO)S(CH2)7CH3 0 4.281 CH3 CF3 H H 0(CO)OCH2CH3 0 4.282 CH3 CF3 H H 0(CO)N(CH2CH3)2 0 4.283 CH3 (CF2)3CF3 H H OH 0 4.284 CH3 CF3 H H S-(4-CI-phenyl) 0 4.285 CH3 CF3 H H SO-(4-CI-phenyl) 0 4.286 CH3 CF3 H H S02-(4-CI-phenyl) 0 4.287 CH3 CF3 H H S-(4-CF3-phenyl) 0 4.288 CH3 CF3 H H SO-(4-CF3-phenyl) 0 4.289 CH3 CF3 H H S02-(4-CF3-phenyl) 0 4.29 CH3 CF3 H H S-(4-N02-phenyl) 0 4.291 CH3 CF3 H H SO-(4-N02-phenyl) 0 4.292 CH3 CF3 H H S02-(4-N02-phenyl) 0 Comp. R, R2 R3 R4 R5 P No. 4.298 CF2CI SCH3 H H OH 0 4.299 CF2H SOCH3 H H OH 0 ' 4.3 CF2CI SOCH3 H H OH 0 4.301 CF2H S02CH3 H H OH 0 4.302 CF2CI S02CH3 H H OH 0 4.303 CF2H SCH2CH3 H H OH 0 4.304 CF2CI SCH2CH3 H H OH 0 4.305 CF2H SOCH2CH3 H H OH 0 4.306 CF2CI SOCH2CH3 H H OH 0 4.307 CF2H S02CH2CH3 H H OH 0 4.308 CF2CI S02CH2CH3 H H OH 0 4.309 CF2H OCH3 H H OH 0 4.31 CF2CI OCH3 H H OH 0 4.311 CF2H OCH2CF3 H H OH 0 4.312 CF2CI OCH2CF3 H H OH 0 4.313 CF2H OCH2CCH H H OH 0 4.314 CF2CI OCH2CCH H H OH 0 4.315 CF2H CN H H OH 0 4.316 CF2CI CN H H OH 0 4.317 CF2H CI H H OH 0 4.318 CF2CI CI H H OH 0 4.319 CF2H OCH3 H H OH 0 4.32 CF2CI OCH3 H H OH 0 4.321 CF3 CH2OCH3 H H OH 0 4.322 CF3 CH2OCH3 H H OH 1 4.323 CF2CI CH2OCH3 H H OH 0 4.324 CF2CI CH2OCH3 H H OH 1 4.325 CF2H CH2OCH3 H H <. oh> 4.326 CF2H CH2OCH3 H H OH 1 4.327 CN CF3 H H OH 0 4.328 SCH3 H H H OH ' 0 Comp. No. R1 R2 R3 R4 R5 5.1 H CF3 H H CH3 5.2 F CF3 H H CH3 5.003 CI CF3 H H CH3 5.4 CHF2 CF3 H H CH3 5.5 CCI3 CF3 H H CH3 5.006 CCIF2 CF3 H H CH3 5.007 CF3 CF3 H H CH3 5.008 CH3 CF3 H H CH3 5.009 CH2CH3 CF3 H H CH3 5.01 CH(CH3)2 CF3 H H CH3 5.011 (CH2)2CH3 CF3 H H CH3 5.12 CH2F CF3 H H CH3 5.13 CH2CI CF3 H H CH3 5.014 CH2Br CF3 H H CH3 5.015 CH2OCOCH3 CF3 H H CH3 5.016 CH2OCH3 CF3 H H CH3 5.017 CH2CH2OCH3 CF3 H H CH3 5.018 CH2SMe CF3 H H CH3 5.019 CH2SOMe CF3 H H CH3 5.02 CH2S02Me CF3 H H CH3 5.021 N(CH3)2 CF3 H H ' CH3 5.022 CH=CH2 CF3 H H CH3 5.23 CH2CH=CH2 CF3 H H CH3 5.24 S02N(CH3)2 CF3 H H CH3 Comp. No. R, R2 R3 R4 R5 5.025 CCH CF3 H H - CH3 5.026 cyclopropyl CF3 H H CH3 5.027 OCH3 CF3 H H CH3 5.028 OPh CF3 H H CH3 5.029 OCHF2 CF3 H H CH3 5.03 C02Me CF3 H H CH3 5.031 OCH2CCH CF3 H H CH3 5.32 CF3 SCH3 H H CH3 5.33 CH3 SCH3 H H CH3 5.34 CF3 SOCH3 H H CH3 5.35 CH3 SOCH3 H H CH3 5.36 CF3 S02CH3 H H CH3 5.37 CH3 S02CH3 H H CH3 5.38 CF3 OCH3 H H CH3 5.39 CH3 OCH3 H H CH3 5.04 CF3 OCH2CF3 H H CH3 5.41 CH3 OCH2CF3 H H CH3 5.42 CF3 OCH2CCH H H CH3 5.43 CH3 OCH2CCH H H CH3 5.44 CF3 CN H H CH3 5.45 CH3 CN H H CH3 5.46 CF3 CI H H CH3 5.47 CH3 CI H H CH3 5.048 H CI H H CH3 5.049 CF3 OCH3 H H CH3 5.05 CH3 OCH3 H H CH3 5.051 CF3 CH3 H H CH3 5.52 H CF3 H CH3 CH3 5.53 H CF3 H CF3 -. CH3 5.54 H CF3 H CH2CH3 CH3 5.55 H CF3 H CF3 CH3 5.56 H CF3 H SCH3 CH3 Comp. No. R, R2 R3 R4 R5 5.57 H CF3 H SOCH3- CH3 5.58 H CF3 H SO2CH3 CH3 5.59 H CF3 H CI CH3 5.06 H CF3 H OCH3 CH3 5.61 H CH3 H CF3 CH3 5.62 H CI H CF3 CH3 5.63 H OCH3 H CF3 CH3 5.64 H SCH3 H CF3 CH3 5.65 H SOCH3 H CF3 CH3 5.66 CF2CI CH3 H H CH3 5.67 CF2CI CH2CH3 H H CH3 5.68 CF2CI SCH3 H H CH3 5.69 CF2CI SOCH3 H H CH3 5.07 CF2CI S02CH3 H H CH3 5.71 CF2CI OCH3 H H CH3 5.72 CF2CI OCH2CF3 H H CH3 5.73 CF2CI OCH2CCH H H CH3 5.74 CF2CI CN H H CH3 5.75 CF2CI CI H H CH3 5.76 CF2CI OCH3 H H CH3 5.077 CF3 CH2OCH3 H H CH3 5.78 CF2CI CH2OCH3 H H CH3 5.79 CF2H CH2OCH3 H H CH3 5.08 CN CF3 H H CH3 5.81 CH3 CF3 H H CH2CH3 5.82 CH3 CF3 H H SCH3 5.83 CH3 CF3 H H SOCH3 5.84 CH3 CF3 H H S02CH3 5.85 CH3 CF3 H H >. H 6.001 CI CF3 H H CH2CH3 6.2 CHF2 CF3 H H CH2CH3 6.3 CCI3 CF3 H H CH2CH3 6.004 CCIF2 CF3 H H CH2CH3 6.005 CF3 CF3 H H CH2CH3 6.006 CH3 CF3 H H CH2CH3 6.007 CH2CH3 CF3 H H CH2CH3 6.008 (CH2)2CH3 CF3 H H CH2CH3 6.009 CH2F CF3 H H CH2CH3 6.01 CH2CI CF3 H H CH2CH3 6.011 CH2OCH3 CF3 H H CH2CH3 6.012 CH2SMe CF3 H H CH2CH3 6.013 CH2S02Me CF3 H H CH2CH3 6.014 CH=CH2 CF3 H H CH2CH3 6.015 CH2CH=CH2 CF3 H H CH2CH3 6.016 CCH CF3 H H CH2CH3 6.017 CF3 SCH3 H H CH2CH3 6.018 , CF3 SOCH3 H H CH2CH3 6.019 CF3 S02CH3 H H CH2CH3 6.02 CF3 OCH3 H H CH2CH3 6.021 CF3 CN H H CH2CH3 6.22 CF3 CI H H CH2CH3 6.23 CF3 OCH3 H H CH2CH3 6.024 CF3 CH3 H H CH2CH3 Comp. No. R1 R2 R3 R4 Rs 6.025 H ■QF3 H CH3 - CH2CH3 6.026 H CF3 H CF3 CH2CH3 6.027 H CF3 H SCH3 CH2CH3 6.028 H CF3 H SOCH3 CH2CH3 6.029 H CF3 H S02CH3 CH2CH3 6.03 H CF3 H CI CH2CH3 6.031 H CF3 H OCH3 CH2CH3 6.032 H CH3 H CF3 CH2CH3 6.033 H CI H CF3 CH2CH3 6.034 H OCH3 H CF3 CH2CH3 6.035 CN CF3 H H CH2CH3 6.036 CI CF3 H H CH(CH3)2 6.037 CHF2 CF3 H H CH(CH3)2 6.038 CCI3 CF3 H H CH(CH3)2 6.039 CCIF2 CF3 H H CH(CH3)2 6.04 CF3 CF3 H H CH(CH3)2 6.041 CH3 CF3 H H CH(CH3)2 6.042 CH2CH3 CF3 H H CH(CH3)2 6.043 (CH2)2CH3 CF3 H H CH(CH3)2 6.044 CH2F CF3 H H CH(CH3)2 6.045 CH2CI CF3 H H CH(CH3)2 6.046 CH2OCH3 CF3 H H CH(CH3)2 6.047 CH2SMe CF3 H H CH(CH3)2 6.048 CH2S02Me CF3 H H CH(CH3)2 6.049 CH=CH2 CF3 H H CH(CH3)2 6.05 Cn2CH=CH2 CF3 H H CH(CH3)2 6.051 CCH CF3 H H CH(CH3)2 6.052 CF3 SCH3 H H CH(CH3)2 6.053 CF3 SOCH3 H H ; CH(CH3)2 6.054 CF3 S02CH3 H H CH(CH3)2 6.055 CF3 OCH3 H H CH(CH3)2 6.056 CF3 CN H H CH(CH3)2 Comp. No. R, R2 R3 R4 R5 6.57 CF3 CI H H > CH(CH3)2 6.58 CF3 OCH3 H H CH(CH3)2 6.59 CF3 CH3 H H CH(CH3)2 6.06 H CF3 H CH3 CH(CH3)2 6.61 H CF3 H CF3 CH(CH3)2 6.62 H CF3 H SCH3 CH(CH3)2 6.63 H CF3 H SOCH3 CH(CH3)2 6.64 H CF3 H S02CH3 CH(CH3)2 6.65 H CF3 H CI CH(CH3)2 6.66 H CF3 H OCH3 CH(CH3)2 6.67 H CH3 H CF3 CH(CH3)2 6.68 H CI H CF3 CH(CH3)2 6.69 H OCH3 H CF3 CH(CH3)2 6.07 CN CF3 H H CH(CH3)2 6.071 CI CF3 H H HNPh 6.72 CHF2 CF3 H H HNPh 6.73 CCI3 CF3 H H HNPh 6.74 CCIF2 CF3 H H HNPh 6.75 CF3 CF3 H H HNPh 6.76 CH3 CF3 H H HNPh 6.077 CH2CH3 CF3 H H HNPh 6.078 (CH2)2CH3 CF3 H H HNPh 6.079 CH2F CF3 H H HNPh 6.08 CH2CI CF3 H H HNPh 6.081 CH2OCH3 CF3 H H HNPh 6.082 CH2SMe CF3 H H HNPh 6.083 CH2S02Me CF3 H H HNPh 6.084 CH=CH2 CF3 H H HNPh 6.085 CH2CH=CH2 CF3 H H HNPh 6.86 CCH CF3 H H HNPh 6.87 CF3 SCH3 H H HNPh 6.88 CF3 SOCH3 H H HNPh Comp. No. R1 R2 R3 R4 Rs 6.089 CF3 S02CH3 H H HNPh 6.09 CF3 OCH3 H H HNPh 6.091 CF3 CN H H HNPh 6.092 CF3 CI H H HNPh 6.093 CF3 OCH3 H H HNPh 6.094 ' CF3 CH3 H H HNPh 6.095 H CF3 H CH3 HNPh 6.096 H CF3 H CF3 HNPh 6.097 H CF3 H SCH3 HNPh 6.098 H CF3 H SOCH3 HNPh 6.099 H CF3 H S02CH3 HNPh 6.1 H CF3 H CI HNPh 6.101 H CF3 H OCH3 HNPh 6.102 H CH3 H CF3 HNPh 6.103 H CI H CF3 HNPh 6.104 H OCH3 H CF3 HNPh 6.105 CN CF3 H H HNPh 6.106 CI CF3 H H HNC(CH3)3 6.107 CHF2 CF3 H H HNC(CH3)3 6.108 CCI3 CF3 H H HNC(CH3)3 6.109 CCIF2 CF3 H H HNC(CH3)3 6.11 CF3 CF3 H H HNC(CH3)3 6.111 CH3 CF3 H H HNC(CH3)3 6.112 CH2CH3 CF3 H H HNC(CH3)3 6.113 (CH2)2CH3 CF3 H H HNC(CH3)3 6.114 CH2F CF3 H H HNC(CH3)3 6.115 CH2C! CF3 H H HNC(CH3)3 6.116 CH2OCH3 CF3 H H HNC(CH3)3 6.117 CH2SMe CF3 H H 6.118 CH2S02Me CF3 H H HNC(CH3)3 6.119 CH=CH2 CF3 H H HNC(CH3)3 6.12 CH2CH=CH2 CF3 H H HNC(CH3)3 Comp. No. R, R2 R3 R" Rs 6.121 CCH CF3 H . H ' HNC(CH3)3 6.122 CF3 SCH3 H H HNC(CH3)3 6.123 CF3 SOCH3 H H HNC(CH3)3 6.124 CF3 S02CH3 H H HNC(CH3)3 6.125 CF3 OCH3 H H HNC(CH3)3 6.126 CF3 CN H H HNC(CH3)3 6.127 CF3 CI H H HNC(CH3)3 6.128 CF3 OCH3 H H HNC(CH3)3 6.129 CF3 CH3 H H HNC(CH3)3 6.13 H CF3 H CH3 HNC(CH3)3 6.131 H CF3 H CF3 HNC(CH3)3 6.132 H CF3 H SCH3 HNC(CH3)3 6.133 H CF3 H SOCH3 HNC(CH3)3 6.134 H CF3 H S02CH3 HNC(CH3)3 6.135 H CF3 H CI HNC(CH3)3 6.136 H CF3 H OCH3 HNC(CH3)3 6.137 H CH3 H CF3 HNC(CH3)3 6.138 H CI H CF3 HNC(CH3)3 6.139 H OCH3 H CF3 HNC(CH3)3 6.14 CN CF3 H H HNC(CH3)3 7.001 H CF3 H H 0 7.002 F CF3 H H 0 7.3 CI CF3 H H 0 7.4 Br CF3 H H 0 7.005 CHF2 CF3 H H 0 7.006 CCI3 CF3 H H 0 7.007 CCIF2 CF3 H H 0 7.8 CF3 CF3 H H 0 7.9 CH3 CF3 H H 0 7.01 CH2CH3 CF3 H H 0 7.011 CH(CH3)2 CF3 H H 0 7.012 (CH2)2CH3 CF3 H H 0 7.013 C(CH3)3 CF3 H H 0 7.014 Ph CF3 H H 0 7.015 CH2F CF3 H H 0 7.16 CH2CI CF3. H HO. 7.17 CH2Br CF3 H H 0 7.018 CH2OH CF3 H H 0 7.019 CH2OCOCH3 CF3 H H 0 7.02 CH2OCOPh CF3 H HO 7.021 CH2OCH3 CF3 H H 0 7.022 CH2OCH2CH3 CF3 H . H 0 Comp. No. R1 R2 ^3 R4 p 7.023 CH2CH2OCH3 CF3 H H 0 - 7.024 CH2SMe CF3 H H 0 7.25 CH2SOMe CF3 H H 0 7.26 CH2S02Me CF3 H H 0 7.27 CH2S02Ph CF3 H H 0 7.028 SCH3 CF3 H HO 7.029 SOCH3 CF3 H H 0 7.03 S02CH3 CF3 H H 0 7.31 N(CH3)2 CF3 H H 0 7.32 CH=CH2 CF3 H H 0 7.33 CH2CH=CH2 CF3 H H 0 7.34 S02N(CH3)2 CF3 H H 0 7.035 CCH CF3 H H 0 7.036 cyclopropyl CF3 H H 0 7.037 OCH3 CF3 H H 0 7.038 OCHF2 CF3 H H 0 7.039 OCH2CCH CF3 H H 0 7.04 H CF2CF3 H H 0 7.041 CI CF2CF3 H H 0 7.42 CHF2 CF2CF3 H H 0 7.43 CCI3 CF2CF3 H H 0 7.44 CCIF2 CF2CF3 H H 0 7.45 CF3 CF2CF3 . H HO 7.46 CH3 CF2CF3 H H 0 7.047 CH2CH3 CF2CF3 H H 0 7.48 CH(CH3)2 CF2CF3 H H 0 7.49 (CH2)2CH3 CF2CF3 H H 0 7.05 C(CH3)3 CF2CF3 H H 0 7.51 CH2F CF2CF3 H H 0 7.52 CH2CI CF2CF3 H H 0 7.053 CH2OH CF2CF3 H H 0 7.054 CH2OCOCH3 CF2CF3 H H 0 Comp. No. R1 R2 R3 R4 p 7.055 CH2OCOPh CF2CF3 H H 0 7.056 CH2OCH3 CF2CF3 H H 0 7.057 CH2OCH2CH3 CF2CF3 H H 0 7.058 CH2SMe CF2CF3 H H 0 7.059 CH2SOMe CF2CF3 H H 0 7.06 CH2S02Me CF2CF3 H H 0 7.061 CH2S02Ph CF2CF3 H H 0 7.62 N(CH3)2 CF2CF3 H H 0 7.63 CH=CH2 CF2CF3 H H 0 7.64 CH2CH=CH2 CF2CF3 H H 0 7.65 S02N(CH3)2 CF2CF3 H H 0 7.066 CCH CF2CF3 H H 0 7.067 cyclopropyl CF2CF3 H H 0 7.068 OCH3 CF2CF3 H H 0 7.069 C02Me CF2CF3 H H 0 7.07 OCH2CCH CF2CF3 H H 0 7.71 H CF2CI H H 0 7.72 CI CF2CI H H 0 7.73 CHF2 CF2CI H H 0 7.74 CCI3 CF2CI H H 0 7.75 CCIF2 CF2CI H H 0 7.76 CF3 CF2CI H H 0 7.77 CH3 CF2CI H H 0 7.078 CH2CH3 CF2CI H H 0 7.079 CH(CH3)2 CF2CI H H 0 7.08 (CH2)2CH3 CF2CI H H 0 7.081 C(CH3)3 CF2CI H H 0 7.82 CH2F CF2CI H H 0 7.83 CH2CI CF2CI H H 0 7.084 CH2OH CF2CI H H 0 7.85 CH2OCOCH3 CF2CI H H 0 7.86 CH2OCOPh CF2CI H H 0 Comp. No. R, R2 R3 R4 p 7.087 CH2OCH3 CF2CI H H 0 - 7.088 CH2OCH2CH3 CF2CI H H 0 7.089 CH2SMe CF2CI H H 0 7.09 CH2SOMe CF2CI H H 0 7.91 CH2S02Me CF2CI H H 0 7.92 CH2S02Ph CF2CI H H 0 7.93 N(CH3)2 CF2CI H H 0 7.94 CH=CH2 CF2CI H H 0 7.95 CH2CH=CH2 CF2CI H H 0 7.96 S02N(CH3)2 CF2CI H H 0 7.097 CCH CF2CI H H 0 7.098 cyclopropyl CF2CI H H 0 7.099 OCH3 CF2CI H H 0 7.1 OCH2CCH CF2CI H H 0 7.101 CF3 CHF2 H H 0 7.102 CH3 CHF2 H H 0 7.103 CH2OCH3 CHF2 H H 0 7.104 CH2CI CHF2 H H 0 7.105 CH2F CHF2 H H 0 7.106 CH3 CF3 H CH3 0 7.107 CI CF3 H CH3 0 7.108 CH3 CF3 CH3 H 0 7.109 CH3 CF3 CI H 0 7.11 OCH3 CF3 CH3 H 0 7.111 CH2OCH3 CF3 CH3 H 0 7.112 CH2OCH3 CF3 CI H 0 7.113 COOCH3 H H H 0 7.114 CF3 SCH3 H H 0 7.115 CH3 SCH3 H H 0 7.116 CF3 SOCH3 H H 0 7.117 CH3 SOCH3 H H 0 7.118 CF3 S02CH3 H H 0 Comp. No. R, R2 R3 R4 p 7.119 CH3 SO2CH3 H H 0 7.12 CF3 OCH3 H H 0 7.121 CH3 OCH3 H H 0 7.122 CF3 OCH2CF3 H H 0 7.123 CH3 OCH2CF3 H H 0 7.124 CF3 OCH2CCH H H 0 7.125 CH3 OCH2CCH H H 0 7.126 CF3 C.N H H 0 7.127 CH3 CN H H 0 7.128 CF3 CI H H 0 7.129 CF3 CI H H 0 7.13 CH3 CI H H 0 7.131 H CI H H 0 7.132 CF3 OCH3 H H 0 7.133 CH3 OCH3 H H 0 7.134 CF3 CH3 H H 0 7.135 H CF3 H CH3 0 7.136 H CF3 H CF3 0 7.137 H CF3 H CH2CH3 0 7.138 H CF3 H CF3 0 7.139 H CF3 H SCH3 0 7.14 H CF3 H SOCH3 0 7.141 H CF3 H S02CH3 0 7.142 H CF3 H CI 0 7.143 H CF3 H OCH3 0 7.144 H CH3 H CF3 0 r 7.145 H CI H CF3 0 7.146 H OCH3 H CF3 0 7.147 H SCH3 H CF3 0 7.148 H SOCH3 H CF3 0 7.149 CH3 (CF2)3CF3 H H 0 7.15 CF2H SCH3 H H 0 Comp. No. R, R2 R3 R4 P 7.183 (CH2)2CH3 CF3 H H 2 . . 7.184 C(CH3)3 CF3 H H 2 7.185 Ph CF3 H H 2 7.186 CH2F CF3 H H 2 7.187 CH2CI CF3 H H 2 7.188 CH2Br CF3 H H 2 7.189 CH2OH CF3 H H 2 7.19 CH2OCOCH3 CF3 H H 2 7.191 CH2OCOPh CF3 H H 2 7.192 CH2OCH3 CF3 H H 2 7.193 CH2OCH2CH3 CF3 H H 2 7.194 CH2CH2OCH3 CF3 H H 2 7.195 CH2SMe CF3 H H 2 7.196 CH2SOMe CF3 H H 2 7.197 CH2S02Me CF3 H H 2 7.198 CH2S02Ph CF3 H H 2 7.199 SCH3 CF3 H H 2 7.2 SOCH3 CF3 H H 2 7.201 S02CH3 CF3 H H 2 7.202 N(CH3)2 CF3 H H 2 7.203 CH=CH2 CF3 H H 2 7.204 CH2CH=CH2 CF3 H H 2 7.205 S02N(CH3)2 CF3 H H 2 7.206 CCH CF3 H H 2 7.207 cyclopropyl CF3 H H 2 7.208 OCH3 CF3 H H 2 7.209 OCHF2 CF3 H H 2 7.21 OCH2CCH CF3 H H 2 8.001 H CF3 H H 8.002 F CF3 H H 8.003 CI CF3 H H 8.004 Br CF3 H H 8.005 CHF2 CF3 H H 8.6 CCI3 CF3 H H 8.7 CCIF2 CF3 H H 8.008 CF3 CF3 H H 8.009 CH3 CF3 H H 8.01 CH2CH3 CF3 H H 8.011 CH(CH3)2 CF3 H H 8.012 (CH2)2CH3 CF3 H H 8.013 C(CH3)3 CF3 H H 8.014 Ph CF3 H H 8.015 CH2F CF3 H H 8.016 CH2CI CF3 H H 8.017 CH2Br CF3 H H 8.018 CH2OH CFi H H 8.019 CH2OCOCH3 CF3 H H 8.02 CH2OCOPh CF3 H H 8.021 CH2OCH3 CF3 H '• H 8.022 CH2OCH2CH3 CF3 H H 8.023 CH2CH2OCH3 CF3 H H 8.024 CH2SMe CF3 H H Comp. No. R, R2 R3 R4 8.025 CH2SOMe GF3. • H H 8.026 CH2S02Me CF3 H H 8.027 CH2S02Ph CF3 H H 8.028 SCH3 CF3 H H 8.029 SOCH3 CF3 H H 8.03 SO2CH3 CF3 H H 8.31 N(CH3)2 CF3 H H 8.32 CH=CH2 CF3 H H 8.33 CH2CH=CH2 CF3 H H 8.34 S02N(CH3)2 CF3 H H 8.035 CCH CF3 H H 8.036 cyclopropyl CF3 H H 8.037 OCH3 CF3 H H 8.038 OCHF2 CF3 H H 8.039 OCH2CCH CF3 H H Comp. No. R1 R2 R3 R4 9.1 H CF3 H H 9.2 F CF3 H H 9.3 CI CF3 H H 9.4 Br CF3 H H 9.005 CHF2 CF3 H H 9.006 CCI3 CF3 H H Comp. No. R1 R2 R3 R4 9.007 CCIF2 CF3 H H 9.008 CF3 CF3 H H 9.009 CH3 CF3 H H 9.01 CH2CH3 CF3 H H 9.011 CH(CH3)2 CF3 H H 9.012 (CH2)2CH3 CF3 H H 9.013 C(CH3)3 CF3 H H 9.014 Ph CF3 H H 9.015 CH2F CF3 H H 9.016 CH2CI CF3 H H 9.017 CH2Br CF3 H H 9.018 CH2OH CF3 H H 9.019 CH2OCOCH3 CF3 H H 9.02 CH2OCOPh CF3 H H 9.021 CH2OCH3 CF3 H H 9.022 Crl2OCn2CH3 CF3 H H 9.023 CH2Cn20Cn3 CF3 H H 9.024 CH2SMe CF3 H H 9.025 CH2SOMe CF3 H H 9.026 CH2S02Me CF3 H H 9.027 CH2S02Ph CF3 H H 9.028 SCH3 CF3 H H 9.029 SOCH3 CF3 H H 9.03 S02CH3 CF3 H H 9.031 N(CH3)2 CF3 H H 9.032 CH=CH2 CF3 H H 9.033 Cn2CH=CH2 CF3 H H 9.034 S02N(CH3)2 CF3 H H 9.035 CCH CF3 H H 9.036 cyclopropyl CF3 H H 9.037 OCH3 CF3 H H 9.038 OCHF2 CF3 H H Domp. No. R, R2 R3 9.039 OCH2CCH CF3 H 'hvsical data (melting points in°C): Comp. No. 1.001 resin 1.005 crystals m.p. 61-62 1.008 oil 1.009 crystals m.p. 75-77 1.01 oil 1.11 crystals m.p. 111-112 1.12 crystals m.p. 87-88 1.13 crystals m.p. 112-114 1.14 oil 1.021 crystals m.p. 128-129 1.23 crystals m.p. 91 -92 1.24 oil 1.026 amorphous 1.028 amorphous 1.03 resin 1.031 crystals m.p. 145-146 1.42 oil 1.43 crystals m.p. 107-110 1.47 crystals m.p. 155-156 1.48 viscous 1.05 crystals m.p. 51 -53 1.06 crystals m.p. >220 1.109 oil 1.195 oil 1.258 crystals m.p. 119-121 1.31 crystals m.p. 92-94 1.312 viscous 1.313 crystals m.p. 137-138 1.314 oil 1.316 resin 1.323 oil 1.334 resin 1.335 crystals m.p. 140-142 1.339 crystals m.p. 137-139 1.341 resin 1.343 crystals m.p. 97-99 1.347 crystals m.p. 135-137 1.349 oil, nD 1.4965 1.351 crystals m.p. 125-127 1.353 resin, nD 1.5289 1.355 crystals m.p. 90-92 1.356 resin 1.358 resin 1.361 oil 1.362 crystals m.p. 139-142 1.371 crystals m.p. 96-97 1.372 resin 1.373 resin 1.374 crystals m.p. 116-1199 1.375 resin 1.376 crystals m.p. >270 1.381 crystals m.p. 117-118 1.383 crystals m.p. 172-173 1.384 resin 1.385 resin 1.386 resin 1.387 resin 1.388 crystals m.p. 102-104 1.389 crystals m.p. , 143-145 1.39 crystals m.p. . 195-197 1.391 solid 1.392 crystals m.p. . 202-206 1.398 crystals m.p. . 137-138 1.399 crystals m.p. . 262-263 1.4 oil 1.401 oil 1.402 oil 1.403 oil 1.404 oil 1.405 viscous 1.406 oil 1.408 oil 1.409 oil 1.41 oil 1.411 crystals m.p. 98-100 1.412 crystals m.p. 130-131 1.413 crystals m.p. 167-170 1.414 crystals m.p. 166-167 1.415 crystals m.p. 91-93 1.418 crystals m.p. 149-150 1.421 crystals m.p. 88-89 1.422 crystals m.p. 175-177 1.423 crystals m.p. 45-47 1.424 crystals m.p. 102-104 2.001 resin 2.003 oil 2.03 crystals m.p. 107-110 2.038 crystals m.p. 111-113 2.043 resin 2.044 crystals m.p. 105-106 2.045 amorphous 3.001 crystals m.p. 95-97 3.54 oil 3.55 crystals m.p. 108-110 3.056 resin, nD 1.5509 4.009 crystals m.p. 107-109 4.01 oil 4.011 oil 4.014 crystals m.p. 148-149 4.021 crystals m.p. 44-45 4.033 crystals m.p. 46-48 4.124 crystals m.p. 46-48 4.328 oil 5.008 resin 5.081 resin 5.83 crystals m.p. 161 -162 5.84 crystals m.p. 215-216 5.85 resin 6.006 crystals m.p. 176-177 6.041 crystals m.p. 186-187 6.076 crystals m.p. 195-196 6.111 crystals m.p. 163-164 7.009 ratio A: B = 2:1 .H-NMR(CDCI3,ppm) SCH3: A: 2.50; B: 2.66. 7.01 ratio A: B = 5:1. H-NMR(CDCI3,ppm) SCH3: A: 2.50; B: 2.64. 7.011 ratio A: B = 9:1. H-NMR(CDCI3,ppm) SCH3: A: 2.46; B: 2.59. 7.021 ratio A: B = 3:1. H-NMR(CDCI3,ppm) SCH3: A: 2.50; B: 2.62. 7.18 ratio A: B = 2:. H-NMR(CDCI3,ppm) S02CH3: A: 3.40; B: 3.58. 7.182 ratio A: B = 9:1. H-NMR(CDCI3,ppm) S02CH3: A: 3.32; B: 3.50. 7.192 ratio A: B = 3:1. H-NMR(CDCI3,ppm) S02CH3: A: 3.40; B: 3.58. 8.009 crystals m.p. 96-97 8.01 amorphous 8.011 oil 8.021 oil 9.009 crystals m.p. 112-113 9.01 amorphous 9.011 amorphous 9.021 oil Biological Examples Example B1: Herbical action before emergence of the plants (pre-emerqence action) Monocotyledonous and dicotyledonous test plants are sown in standard soil in plastic pots. Immediately after sowing, the test substances are sprayed on (500 I of water/ha) as an aqueous suspension (prepared from a 25% wettable powder (Example F3, b) according to WO 97/34485) or emulsion (prepared from a 25% emulsion concentrate (Example F1, c)), corresponding to a dosage of 2 kg of AS/ha. The test plants are then grown under optimum conditions in a greenhouse. After a test period of 3 weeks, the test is evaluated with a nine-level scale of ratings (1 = complete damage, 9 = no effect). Ratings of 1 to 4 (in particular 1 to 3) mean good to very good herbicidal action. Table B1: pre-emerqence action: Cyperus Setaria Sinapis Solanum Stellaria Test plant Avena Active compound No. 1.009 2 1.376 2 4.009 1 7.009 4 1.381 4 1.011 2 5.008 2 4.021 2 1.010 2 1.021 4 1.398 2 1.195 2 1 2 1 2 1 2 1 2 2 2 1 3 2 3 1 2 1 2 2 1 1 1 1 1 . 1 1 2 I 2 1 2 2 I 2 1 1 « I 2 2 1 1 3 1 1 I 1 1 1 I 2 4.124 2 1 2 2 1 2 1.411 3 2 1 2 12 1.042 4 2 2 1 1 4 1.023 2 2 2 1 1 2 1.109 2 2 2 2 1 3 1.313 3 2 1 1 2 1.401 2 1 2 1 2 1.404 2 1 2 1 2 1.400 2 1 2 1 2 1.403 2 1 1 1 2 1.405 2 1 1 1 2 1.406 2 1 1 1 2 1.402 2 1 2 1 2 1.005 4 1 1 1 1 1.043 4 2 1 2 1 2 1.409 1 1 1 1 1 1.41 2 1 1 1 1 1.06 2 1 2 1 1 7.192 4 2 2 3 2 2 7.021 1 1 1 1 1 1 ne results are obtained when the com pounds of the formula I are formulated according to Examples F2 and F4 to F8 according to WO 97/34485. Example B2: Post-emergence herbicidal action Monocotyledonous and dicotyledonous test plants are grown in plastic pots with standard soil in a greenhouse and, in the 4- to 6-leaf stage, are sprayed with an aqueous suspension of the test substances of the formula I, prepared from a 25% wettable powder (Example F3, b) according to WO 97/34485) or with an emulsion of the test substances of the formula I, prepared from a 25% emulsion concentrate (Example F1, c) according to WO 97/34485), corresponding to a dosage of 2 kg of AS/ha (500 I of water/ha). The test plants are then grown further under optimum conditions in a greenhouse. After a test period of about 18 days, the test is evaluated with a nine-level scale of rating (1 = complete damage, 9 = no effect). Ratings of 1 to 4 (in particular 1 to 3) mean good to very good herbicidai action. In this test, the compounds of the formula I show strong herbicidai action. Table B2: post-emergence action: Test plant Avena Setaria Solanum Sinapis Stellaria Active compound No. 1.009 1 1 1 2 1.376 1 2 2 2 4.009 1 1 1 1 1.026 3 1 1 2 7.009 3 2 1 1 1.381 2 2 2 2 2 1.011 2 2 2 2 2 5.008 2 3 1 2 5.085 3 2 2 2 4.021 2 2 1 2 1.012 3 2 2 2 1.010 2 2 2 4 4.010 3 3 2 2 2 1.021 2 4 2 2 1.398 2 2 2 2 1.195 2 2 2 2 4.124 2 2 1 2 1.411 2 2 2 2 1.008 2 2 2 2 6.006 2 5 2 2 2 5.081 3 2 1 2 1.042 2 2 2 1 v 2 1.023 2 2 2 2 1.109 2 2 2 2 1.313 2 2 2 2 1.401 2 2 2 2 2 1.404 2 2 1 -1 2 1.400 2 2 2 2 1.403 2 2 2 2 1.403 2 2 2 2 1.405 2 2 2 2 1.406 2 2 1 2 1.402 2 2 2 2 1.001 3 2 2 2 1.005 2 2 2 2 1.362 3 2 2 2 1.043 2 2 2 2 1.409 2 1 1 2 1.410 1 1 1 1 1.060 2 1 1 2 7.192 2 3 3 2 2 7.021 1 2 1 2 1.048 2 1 1 2 The same results are obtained when the compounds of the formula I are formulated according to Examples F2 and F4 to F8 according to WO 97/34485. Example B3: Herbicidal action before emergence of the plants (pre-emerqence action) Monocotyledonous and dicotyledonous test plants are sown in pots in standard soil. Immediately after sowing, the test substances are sprayed on (500 I of spray liquor/ha) as an aqueous suspension, prepared from a wettable powder WP10 corresponding to the desired dosage (250 g of a.i./ha). The test plants are then grown under optimum conditions in a greenhouse. After a test period of 3 weeks, the test is evaluated with a nine-ievel scale of ratings (1 = complete damage, 9 = no effect). Ratings of 1 to 4 (in particular 1 to 3) mean good to very good herbicidal action, 7-9 mean good tolerance. Table B3: Pre-emergence action: Test plant Abutilon Amar- Cheno-anthus podium Kochia Sida Stellaria Dose [g of AS/ha] Active compound Na 1.355 1 1.347 2 1.335 1 1.349 1 1.339 2 1.341 3 1.343 1 1 2 2 3 1 9 4 1 1 5 4 7 9 9 2 4 2 2 2 4 3 2 1 7 5 1 1 5 250 250 250 250 250 250 250 The same results are obtained when the compounds of the formula I are formulated according to Examples F2 and F4 to F8 according to WO 97/34485. Example B4: Herbicidal action after the emergence of the plants (post-emergence action) Monocotyledonous and dicotyledonous test plants are sown in pots in standard soil. In the 2-3-leaf stage of the test plants, the test substances are sprayed on (500 I of spray liquor/ha) as an aqueous suspension, prepared from a wettable powder WP10 according to the desired dosage (250 g of a.i./ha). 0.2% of X77 is added as wetting agent to the spray liquor. The test plants are then grown under optimum conditions in a greenhouse. After a test period of 3 weeks, the test is evaluated with a nine-level scale of ratings (1 = complete damage, 9 = no effect). Ratings of 1 to 4 (in particular 1 to 3) mean good to very good herbicidal action, 7-9 mean good tolerance. Table B4: Post-emergence arrtnn: Test plant Abutilon Amar- Cheno- Kochia Setaria Stellaria Dose anthus podium [g of AS/ha] Active compound No. 1.355 2 2 2 3 2 3 250 1.347 3 2 2 2 3 3 250 1.335 3 2 2 2 2 3 250 1.349 2 2 2 2 2 3 250 1.339 2 2 3 1 4 3 250 1.351 5 2 3 3 3 3 250 1.341 5 2 3 4 5 4 250 1.343 3 2 2 3 9 3 250 1.361 2 2 2 2 2 3 250 The same results are obtained when the compounds of the formula I are formulated according to Examples F2 and F4 to F8 according to WO 97/34485. WE CLAIM: 1. A pyridine ketone compound of the formula I in which each R independently is C1-C6alkyl, C2-C6alkenyl, C2-C6haloalkenyl, C2-C6alkynyl, C2-C6 haloalkynyl, C3-C6cycloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylthio, C1-C6alkylsulfinyl, C,-C6alkylsulfonyl, C,-C6haloalkyl, C1-C6haloalkylthio, C,-C6haloalkylsulfinyl, C1-C6 haloalkylsulfonyl, Ci-C6alkoxycarbonyl, C1-C6alkylcarbonyl, C1-C6alkylamino, di-C1-C6alkylamino, Ci-C6alkylaminosulfonyl, di-C1-C6alkylaminosulfonyl, -N(R,)-S-R2, -N(R3)-SO-R4, -N(R5)-S02-R6, nitro, cyano, halogen, hydroxyl, amino, formyl, hydroxy-Ci-C6alkyl, Ci-C6 alkoxy-C1-C6alkyl, C1-Cgalkoxycarbonyloxy-C1-Cealkyl, C1-C6alkylthio-Ci-C6alkyl, C1-C6 alkylsulfinyl-C1-C6alkyl, Ci-C6alkylsulfonyl-Ci-C6alkyl, thiocyanato-C1-C6alkyl, cyano-C1-C6 alkyl, oxiranyl, C3-C6alkenyloxy, C3-C6alkynyloxy, Cj-Cealkoxy-CpCsalkoxy, cyano-C1-C6 alkenyloxy, CpCealkoxycarbonyloxy-CpCgalkoxy, C3-C6alkynyloxy, cyano-C1-C6alkoxy, Q-Q alkoxycarbonyl-Ci-C6alkoxy, CpCealkylthio-Ci-Cgalkoxy, alkoxycarbonyl-C] -C6alkylthio, alkoxycarbonyl-Ci-C6alkylsulfinyl, alkoxycarbonyl-C1-C6alkylsulfonyl, Ci-C6alkylsulfonyloxy, Ci-C6haloalkylsulfonyloxy, phenyl, benzyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, benzylthio, benzylsulfinyl or benzylsulfonyl, where the phenyl groups may be mono- or polysubstituted by halogen, methyl, ethyl, trifluoromethyl, methoxy or nitro, or R is a five- to ten-membered monocyclic or fused bicyclic ring system, which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, where the ring system is either attached directly to the pyridine ring or attached to the pyridine ring via a C1-C4alkylene group, and where each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and where the ring system for its part may be mono-, di- or trisubstituted by C1-C6alkyl, Ci-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C|-C6alkoxy, Ci-C6haloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, C1-C6alkylfhio, Ci-C6haloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5alkoxyalkylthio, C3-C5 acetylalkylthio, C3-C6alkoxycarbonyIalkylthio, C2-C4cyanoalkylthio, C1-C6alkylsulfinyl, Ci-C6haloalkylsulfinyl, C|-C6alkylsulfonyl, C1-C6haloalkylsulfonyl. aminosulfonyl, Ci-C2alkylaminosulfonyl, C2-C4dialkylaminosulfonyl, Ci-C3alkylene-R7, NR8R9, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C|-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; m is 1, 2, 3 or 4; p is 0 or 1; Ri, R3 and R5 independently of one another are hydrogen or C1-C6alkyl; R2 is NR10Rii, C,-C6alkoxy, C,-C6haloalkoxy, C,-C6alkyl, C,-C6haloalkyl, C3~ C6alkenyl, C3-C6 haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C3-C6cycloalkyl or phenyl, where phenyl for its part may be substituted by C,-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro; R4 is NR|2R|3, C,-C6alkoxy, C1-C6haloalkoxy, C,-C6alkyl, C,-C6haloalkyl, C3-C6alkenyl, C3-C6 haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C3-C6cycloalkyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, C1-C3haloalkyl, C|-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro; R6isNRl4R|5, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkyl, C,-C6haloalkyl, C3- C6alkenyl, C3-C6 haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C3-C6cycloalkyl or phenyl, where phenyl for its pari may be substituted by C1-C3alkyl, C|-C3haloalkyl, Ci-C3alkoxy, C,-C3haloalkoxy, halogen, cyano or nitro; R7 is C1-C3alkoxy, C2-C4alkoxycarbonyl, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, C]-C3haloalkyl, C|-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro; R8, Rio, R12 and Ri4 independently of one another are hydrogen or C1-C6alkyl; R9, Ri i, R|3 and Ri5 independently of one another are C1-C6alkyl or CpC^lkoxy; Q is the group Q2 in which Yis~CH2or~CH2~CH2-; A is CH2; R240 is hydrogen; R24i, R242, R243, are hydrogen; R23 is hydroxyl, OM+, halogen, cyano, SCN, OCN, C,-C12alkoxy, C1-C4alkoxycarbonyl-C1-C4 alkoxy, C1-C12alkylthio, C,-Chalkylsulfinyl, C1-C,2alkylsulfonyl, C|-C,2haloalkylthio, C1-Ci2haloalkylsulfinyl, C1-C,2haloalkylsulfonyl, C1-C6alkoxy-C1-C6alkylthio, C1-C6alkoxy-C|-C6 alkylsulfinyl, Ci-C6alkoxy-C1-C6alkylsulfonyl, C2-C12alkenylthio, C2-Ci2alkenylsulfinyl, C2-Ct2 alkenylsulfonyl, C2-C|2alkynylthio, C2-C,2alkynylsulfinyl, C2-C12alkynylsulfonyl, C2- C|2haloalkenylthio, C2-Ci2haloalkenylsulfinyl, C2-Ci2haloalkeny lsulfony 1, C1-C4alkoxycarbonyl-Ci-C4alkylthio, C1-C4alkoxycarbonyl-C|-C4alkylsulfinyl, C1-C4alkoxycarbony 1-C, -C4alkylsulfony 1, (C, -C4alkoxy)2P(0)0, C, -C4alkyl-(C, -C4alkoxy)P(0)0, H(C, -C4alkoxy)P(0)0, R44R45N, R75R76NNH-, R46R47NC(0)0-, R77R78NC(0)NH-, C,-C4alkyl-S(0)2NR48, C,-C4haloalkyl-S(0)2NR49, C,-C4alkyl-S(0)20, C1-C4haloalkyl-S(0)20, C,-Ci8alkylcarbonyloxy, where the alkyl group may be substituted by halogen, C1-C6alkoxy, C1-C6alkylthio or cyano, C2-Ci8alkenylcarbonyloxy, C2-C18alkynylcarbonyloxy, C3-C6cycloalkylcarbonyloxy, CpC^alkoxycarbonyloxy, C1-C12alkylthiocarbonyloxy, C,-C12alkylthiocarbamoyl, C,-C6alkyl-NH(CS)N(C,-C6alkyl)-NH-, di-C1-C6alkyl-N(CS)N(C,-C6alkyl)-NH-, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by C,-C4alkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4alkylcarbonyl, Ci-C4alkoxycarbonyl, C|-C4alkylamino, di-Ci-C4alkylamino, C1-Qalkylthio, C,-C4alkylsulfinyl, C1-C4alkylsulfony 1, C,-C4alkyl-S(0)20, C1-C4haloalkylthio, C|-C4haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C,-C4haloalkyl-S(0)20, C1-C4alkyl-S(0)2NII. (VQalkyl-SCO^NCCi-C, alkyl), halogen, nitro or cyano, or a group Ar6-thio, Ar7-sulfinyl, Ar8-sulfonyl, -OCO-Ar9 or NH-Ar]0 in which Ar6, Ar7, Ar8, Ar9 and Ari0 independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by C,-C6alkyl, C,-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-Qhaloalkynyl, C1-C6alkoxy, C1-C6haloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, CrC6alkylthio, C1--C()haloalkylthio, C3-C6alkenylthio, C3- C6haloalkenylthio, C3-C6alkynylthio, C2-C5 alkoxyalkylthio, C3-Csacetylalkylthio, C3- C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, CrC6alkylsulfinyl, Cr C6haloalkylsulfinyl, C|-C6alkylsulfonyl, C|-C6haloalkylsulfonyl, aminosulfonyl, Cr C2alkylaminosulfonyl, C2-C4dialkylaminosulfonyl, Q-C^alkylene-Rso, NR5iR52, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by CrC3alkyl, CrC3haloalkyl. Cr C3alkoxy, C1--C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; R50 is CrC3alkoxy, C2-C4alkoxycarbonyl, C1--C3alkylthio, CrC3alkylsulfinyl, Cr C3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C|-C3alkyl, CrC3haloalkyl, CrC3 alkoxy, CrC3haloalkoxy, halogen, cyano or nitro; R51 is hydrogen or CrC6alkyl; R52 is C1--C(lalkyl or CrC6alkoxy; R46, R44 , R4X, R49, R75 and R77 independently of one another are hydrogen or Cr C4alkyl; R47, R45, R76 and R7g independently of one another are hydrogen, CrC1-2alkyl, hydroxyl, C|-C|2alkoxy, C3-Cc1alkenyloxy or C3-C6alkynyloxy; or R,(4 and R45 together or R46 and R47 together or R75 and R76 together or R77 and R78 together are pyrrolidino, piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups; or is the group Q4 in which R30 is hydroxyl, 0"M+, halogen, cyano, SCN, OCN, CrCl2alkoxy, Cr C4alkoxycarbonyl-C1-C4 alkoxy, C1--Chalkylthio, C1-C|2alkylsulfinyl» C1-CI2alkylsulfonyl, C,-C,2haloalkylthio, C1-C|2haloalkylsulfinyl, C,-Cl2haloalkylsulfonyl, C1-C6alkoxy-C|-C6alkylthio, C1-C6alkoxy-C1-C6alkylsulfinyl, C]-C6alkoxy-C1--C6alkylsulfonyl, C2-C1-2alkenylthio, C2-C1-2alkenylsulfinyl. C2-C|2 alkenylsulfonyl, C2-C1-2alkynylthio, C2-C1-2alkynylsulfinyl, C2-C12alkynylsulfonyl, C2-C12haloalkenylthio, C2-C1-2haloalkenylsulfinyl, C2-C12haloalkenylsulfonyl, C1-C4alkoxycarbony 1-C1 -C4alkylthio, C1 -C4alkoxycarbonyl-C x-C4alkylsulfiny 1, C1 -C4alkoxycarbonyl-C, -C4alkyIsulfonyl, (C, -C4alkoxy)2P(0)0, C,-C4alkyl-(C,-C4alkoxy)P(0)0, H(C,-C4alkoxy)P(0)0, R62R63N, R83R84NNH-, R64R63NC(0)0-, R85R86NC(0)NH-, C,-C4alkyl-S(0)2NR66, C1-C4haloalkyl-S(0)2NR67, C,-C4alkyl-S(0)20, C,-C4haloalkyl-S(0)20, C,-C|8alkylcarbonyloxy, where the alkyl group may be substituted by halogen, C1-C6alkoxy, C1-C6alkylthio or cyano, C2-C)8alkenylcarbonyloxy, C2-C1-galkynylcarbonyloxy, C3-C(,cycloalkylcarbonyloxy, C1-C12 alkoxycarbonyloxy, C\-C12alkylthiocarbonyloxy, C1 -C, 2alkylthiocarbamoy 1, C, -C6alkyl-NH(CS )N(C, -C6alkyl)-NH-, di-C1-C6alkyl-N(CS)N(C,-C6alkyl)-NH-, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfmyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by C1-C4alkyl, C1-C4haloalkyl, Ct-C4alkoxy, C1-C4haloalkoxy, C1-C4alkylcarbonyl, C1-C4alkoxycarbonyl, C|-C4alkylamino, di-C1-C4alkylamino, C1-C4alkylthio. C,-C4alkylsulfinyl. C,-C4alkyIsulfonyl, C,-C4alkyl-S(0)20, C,-C4haloalkylthio, C1-C4haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4haloalkyl-S(0)20, C1-C4alkyl-S(0)2NH, C1-C4alkyl-S(0)2N(C1-C4 alkyl), halogen, nitro or cyano, or a group Ar(6-thio, Ar17-sulfinyl, ArI8-sulfonyl, -OCO-Arl9 or NH-Ar2o in which Ar)6, Arn, Ar18, Ar19 and Ar20 independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by C,-C6alkyl, C,-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3- C6haloalkynyl, C1-C6alkoxy, CpCJialoalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, C1-C6alkylthio, C1-Cfihaloalkylthio, C3-C6alkenylthio, C3- C6haloalkenylthio, C3-C6alkynylthio, C2-C5 alkoxyalkylthio, C3-C5acetylalkylthio, C3- C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, C|-C6alkylsulfinyl, C1- C6haloalkylsulfinyl, C|-C6alkylsulfonyl, C|-C6haloalkylsulfonyl, aminosulfonyl, C1- C2alkylaminosulfonyl, C2-C4dialkylaminosulfonyl, C1-C3alkylene-R6g, NR69R70, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C,-C3alkyl, C1-C3haloalkyl, C1- C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; R68 is C|-C3alkoxy, C2-C4alkoxycarbonyl, C,-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, C|-C3haloalkyl, C1-C3 alkoxy, C|-C3haloalkoxy, halogen, cyano or nitro; R70 is hydrogen or C1-C6alkyl; R6, is C|-C6alkyl or C1--C6alkoxy; R64 R62, R66 - R67, R83 and R85 independently of one another are hydrogen or C1- C4alkyl; R65, R63, R84 and R86 independently of one another are hydrogen, C1-C1-2alkyl, hydroxyl, C1-C|2alkoxy, C3-Cflalkenyloxy or C3-C6alkynyloxy; or R62 and R63 together or RA4 and R65 together or R83 and R84 together or R83 and R86 together are pyrrolidino, piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups; R33 and R34 independently of one another are C1--C3alkyl, C2-C6alkenyl,; and R35 is C|-C3alkyl, C3-C6alkenyl, and agronomically acceptable salts M+ and all stereoisomers and tautomers of the compounds of the formula I. 2. A hcrbicidal and plant-growth-inhibiting composition, which contains 0.1 to 99% by weight of a compound of the formula I as claimed in claim 1, 1 to 99.9% by weight, of a solid or liquid formulation auxiliary and 0 to 25% by weight of a surfactant. 3. A method for controlling undesirable plant growth, wherein a herbicidally effective amount of an active compound of the formula I or a composition which contains this active compound is applied to the plants or their habitat.

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