EP1976819A2 - Cyclopentane-1,3-dione substitue par 2,4,6-trialkylphenyle - Google Patents

Cyclopentane-1,3-dione substitue par 2,4,6-trialkylphenyle

Info

Publication number
EP1976819A2
EP1976819A2 EP07702572A EP07702572A EP1976819A2 EP 1976819 A2 EP1976819 A2 EP 1976819A2 EP 07702572 A EP07702572 A EP 07702572A EP 07702572 A EP07702572 A EP 07702572A EP 1976819 A2 EP1976819 A2 EP 1976819A2
Authority
EP
European Patent Office
Prior art keywords
alkyl
substituted
optionally
alkoxy
methyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP07702572A
Other languages
German (de)
English (en)
Inventor
Reiner Fischer
Stefan Lehr
Dieter Feucht
Ulrich Görgens
Olga Malsam
Alfred Angermann
Guido Bojack
Alan Graff
Christian Arnold
Thomas Auler
Martin Jeffrey Hills
Heinz Kehne
Christopher Hugh Rosinger
Jan Dittgen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer CropScience AG
Original Assignee
Bayer CropScience AG
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Filing date
Publication date
Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Publication of EP1976819A2 publication Critical patent/EP1976819A2/fr
Withdrawn legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/703—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups
    • C07C49/747—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups containing six-membered aromatic rings
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/703—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups
    • C07C49/707—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups a keto group being part of a three- to five-membered ring
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
    • A01N35/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing keto or thioketo groups as part of a ring, e.g. cyclohexanone, quinone; Derivatives thereof, e.g. ketals
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    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing within the same carbon skeleton a carboxylic group or a thio analogue, or a derivative thereof, and a carbon atom having only two bonds to hetero atoms with at the most one bond to halogen, e.g. keto-carboxylic acids
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    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/20—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom three- or four-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
    • A01N43/26—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
    • A01N43/28—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
    • A01N43/30—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3 with two oxygen atoms in positions 1,3, condensed with a carbocyclic ring
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
    • A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/14—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing aromatic radicals
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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
    • C07C45/46—Friedel-Crafts reactions
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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/657—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings
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    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/657—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings
    • C07C49/665—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings a keto group being part of a condensed ring system
    • C07C49/67—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings a keto group being part of a condensed ring system having two rings, e.g. tetralones
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/013—Esters of alcohols having the esterified hydroxy group bound to a carbon atom of a ring other than a six-membered aromatic ring
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    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
    • C07C69/757—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
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    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/20—Oxygen atoms
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    • C—CHEMISTRY; METALLURGY
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
    • C—CHEMISTRY; METALLURGY
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    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/08—Esters of oxyacids of phosphorus
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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14—The ring being saturated
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    • C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/04—One of the condensed rings being a six-membered aromatic ring
    • C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
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    • C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/14—All rings being cycloaliphatic
    • C07C2602/24—All rings being cycloaliphatic the ring system containing nine carbon atoms, e.g. perhydroindane
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    • C07C2602/14—All rings being cycloaliphatic
    • C07C2602/26—All rings being cycloaliphatic the ring system containing ten carbon atoms

Definitions

  • the present invention relates to novel 2,4,6-trialkylphenyl-substituted cyclopentane-1,3-diones, to a plurality of processes for their preparation and to their use as pesticides and / or herbicides.
  • the invention also relates to novel selective herbicidal active substance combinations which contain 2,4,6-trialkylphenyl-substituted cyclopentane-1,3-dione derivatives on the one hand and at least one crop plant compatibility-improving compound on the other hand and with particularly good success for selective weed control in various crops can be used.
  • Y is methyl or ethyl
  • X and Y are ethyl
  • A is hydrogen, in each case optionally halogen-substituted alkyl, alkenyl, alkoxyalkyl, alkylthioalkyl, saturated or unsaturated, optionally substituted cycloalkyl in which optionally at least one ring atom is replaced by a heteroatom,
  • B is hydrogen, alkyl or alkoxyalkyl, or
  • a and B together with the carbon atom to which they are attached, represent a saturated or unsaturated unsubstituted or substituted cycle, optionally containing at least one heteroatom,
  • a and eil together represent optionally substituted alkanediyl or alkenediyl, which may optionally be interrupted by a heteroatom,
  • Q 1 and Q 1 independently of one another represent hydrogen or alkyl
  • Y is methyl
  • a and B together with the carbon atom to which they are attached represent a saturated or unsaturated, 4- to 8-membered unsubstituted or substituted cycle
  • a and Q * together represent optionally substituted C2-C6-alkanediyl or C2-C6-alkenediyl, which may optionally be interrupted by heteroatoms
  • B and Q ⁇ independently represent hydrogen or alkyl
  • G is hydrogen (a) or one of the groups
  • E is a metal ion equivalent or an ammonium ion
  • L is oxygen or sulfur
  • M is oxygen or sulfur
  • R 1 is each optionally halogen-substituted alkyl, alkenyl, alkoxyalkyl,
  • R.2 is in each case optionally halogen-substituted alkyl, alkenyl, alkoxyalkyl, polyalkoxyalkyl or in each case optionally substituted cycloalkyl, phenyl or benzyl,
  • R 3, R 4 and R 4 independently of one another are each optionally halogen-substituted alkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkenylthio, cycloalkylthio or in each case optionally substituted phenyl, benzyl, phenoxy or phenylthio
  • R ⁇ and R7 are each independently hydrogen, each optionally halogen-substituted alkyl, cycloalkyl, alkenyl, alkoxy, alkoxyalkyl, optionally substituted phenyl, optionally substituted benzyl, or together with the N-atom to which they are attached, for an optionally interrupted by oxygen or sulfur cycle.
  • the compounds of the formula (1) can be present in different compositions as geometric and / or optical isomers or mixtures of isomers, which can optionally be separated in a customary manner. Both the pure isomers and the mixtures of isomers, their preparation and use and agents containing them are the subject of the present invention. In the following, however, for the sake of simplicity, reference is always made to compounds of the formula (I), although both the pure compounds and, if appropriate, mixtures with different proportions of isomeric compounds are meant.
  • the compounds of the formula (I) may be present in the two isomeric forms of the formulas (I-A) and (I-B), depending on the position of the substituent G,
  • the compounds of the formulas (I-A) and (I-B) can be present both as mixtures and in the form of their pure isomers. If desired, mixtures of the compounds of the formulas (I-A) and (I-B) can be separated by physical methods, for example by chromatographic methods.
  • A, B, Q 1 , Q 2 , E, L, M, X, Y, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 have the meanings given above.
  • A, B, Q 1, Q 2 , X and Y have the abovementioned meaning
  • A, B, QI, Q 2 , X and Y are as defined above, and
  • R 8 is alkyl (in particular C 1 -C 6 -alkyl),
  • R.1 has the meaning given above and
  • Hal is halogen (especially chlorine or bromine)
  • R 1 has the meaning given above
  • R 2 and M have the meanings given above, if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder;
  • R3 has the meaning given above
  • Hal is halogen (especially chlorine or bromine),
  • Me is a mono- or divalent metal (preferably an alkali metal or alkaline earth metal such as lithium, sodium, potassium, magnesium or calcium),
  • Rlo, RH, RI 2 are independently hydrogen or alkyl (preferably C j -Cg- alkyl),
  • novel compounds of the formula (I) have very good activity as pesticides, preferably as insecticides, acaricides and herbicides.
  • n stands for a number 0, 1, 2, 3, 4 or 5
  • a 1 represents one of the divalent heterocyclic groupings outlined below,
  • n is a number 0, 1, 2, 3, 4 or 5
  • a 2 is optionally substituted by Ci-C 4 alkyl and / or Ci-C 4 -alkoxy-carbonyl and / or Ci-C 4 - alkenyloxy-carbonyl-substituted alkanediyl having 1 or 2 carbon atoms,
  • R 14 is hydroxy, mercapto, amino, C 1 -C 6 -alkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -alkylamino or di- (C 1 -C 4 -alkyl) -amino,
  • R.15 is hydroxy, mercapto, amino, QC 7 -alkoxy, Ci-C 6 alkenyloxy, C 6 alkenyloxy-Ci-C 6 - alkoxy, Ci-C 6 alkylthio, Ci-C 6 -alkylamino or Is di- (C 1 -C 4 -alkyl) amino,
  • R.16 is optionally C 1 -C 4 -alkyl substituted by fluorine, chlorine and / or bromine,
  • Rl7 is hydrogen, in each case optionally substituted by fluorine, chlorine and / or bromine-substituted CrCe- alkyl, C 2 -C ⁇ rAlkenyl or C 2 -C 6 -A] kinyl, Ci-C 4 -A] koxy-C 1 -C 4 -alkyl, dioxolanyl -C r C 4 alkyl,
  • R! 8 represents hydrogen, in each case optionally substituted by fluorine, chlorine and / or bromine-substituted C 6 - alkyl, C 2 -C 6 alkenyl or C 2 -C 6 alkynyl, Ci-C4-alkoxy-Ci-C 4 - alkyl, dioxolanyl-C 1 -C 4 -alkyl, furyl, furyl-C 1 -C 4 -alkyl, thienyl, thiazolyl, piperidinyl, or optionally phenyl, substituted by fluorine, chlorine and / or bromine or C 1 -C 4 -alkyl stands, R ⁇ and R 18 also together are in each case optionally represented by C 1 -C 4 -alkyl, phenyl, furyl, an annulated benzene ring or by two substituents which, together with the carbon atom to which they are bonded, have a 5- or 6- form a substituted carboxy group
  • RL9 is hydrogen, cyano, halogen, or represents in each case optionally substituted by fluorine, chlorine and / or bromine-substituted C r C 4 alkyl, C 3 -C 6 cycloalkyl or phenyl,
  • R ⁇ O is hydrogen, in each case optionally substituted by hydroxy, cyano, halogen or C 1 -C 4 -alkoxy-substituted C 1 -C 6 -alkyl, C 1 -C 6 -cycloalkyl or tri- (C 1 -C 4 -alkyl) -silyl,
  • R 1 is hydrogen, cyano, halogen, or is in each case optionally substituted by fluorine, chlorine and / or bromine-substituted C 1 -C 4 -alkyl, C 3 -C -cycloalkyl or phenyl,
  • X 1 represents nitro, cyano, halogen, C r C 4 alkyl, C r C 4 haloalkyl, C r C 4 -alkoxy or C r C 4 halo-alkoxy,
  • X 2 represents hydrogen, cyano, nitro, halogen, Ci-C4-alkyl, Ci-GpHalogenalkyl, C r C 4 alkoxy or Ci-C is 4 haloalkoxy,
  • X 3 represents hydrogen, cyano, nitro, halogen, Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C 4 alkoxy or Ci-C is 4 haloalkoxy,
  • R 22 is hydrogen or C 4 -alkyl r C
  • R 23 is hydrogen or C 4 -alkyl r C
  • R 2 ⁇ is hydrogen, in each case optionally substituted by cyano, halogen or Ci-C 4 alkoxy-substituted Ci-Ce-alkyl, C, -C 6 alkoxy, dQ-alkylthio, C, -C 6 alkylamino or di (Ci C 4 -C 6 -alkyl) -amino, or in each case optionally substituted by cyano, halogen or C 1 -C 4 -alkyl-substituted C 3 -C 6 -cycloalkyl, C 3 -C 6 -cycloalkyloxy, C 3 -C 6 -cycloalkylthio or C 3 -C 6 -cycloalkylamino,
  • R ⁇ 2 is hydrogen, optionally cyano-, hydroxyl-, halogen or Ci-C4 alkoxy-substituted Ci-C 6 -alkyl, in each case optionally cyano- or halogen-substituted C 3 -C 6 alkenyl or C 3 -C 6 -AIkUIyI or optionally cyano-, halogen or Ci-C 4 -alkyl-substituted C 3 -C 6 cycloalkyl,
  • R ⁇ 2 is hydrogen, optionally cyano-, hydroxyl-, halogen or Ci-C4 alkoxy-substituted Ci-C 6 -alkyl, in each case optionally cyano- or halogen-substituted C 3 -C 6 alkenyl or C 3 -C 6 alkynyl optionally substituted by cyano, halogen or Ci-C 4 -alkyl-substituted C 3 -C 6 - cycloalkyl, or optionally substituted by nitro, cyano, halogen, Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C 4 - alkoxy or Ci-C4-haloalkoxy-substituted phenyl, or 2 ⁇ is optionally substituted by Ci-C 4 alkyl in each case is C 2 -C ö alkanediyl or oxaalkanediyl CVCs-together with R,
  • X 4 represents nitro, cyano, carboxy, carbamoyl, formyl, sulfamoyl, hydroxy, amino, halogen, Ci-C 4 - alkyl, C] -C 4 haloalkyl, Ci-C4-alkoxy or Ci-C 4 -Halogena] koxy stands, and
  • X 5 represents nitro, cyano, carboxy, carbamoyl, formyl, sulfamoyl, hydroxy, amino, halogen, Ci-C 4 - alkyl, C r C 4 haloalkyl, C r C 4 alkoxy or Ci-C is 4 -haloalkoxy.
  • the compounds of the invention are generally defined by the formula (I). Preferred substituents or ranges of the radicals listed in the formulas mentioned above and below are explained below:
  • X is preferably methyl
  • Y is preferably methyl or ethyl
  • X and Y are both preferably ethyl
  • A preferably represents hydrogen or respectively optionally halogen-substituted C 1 -C 12 -alkyl, C 3 -CG-alkenyl, C ⁇ Cio-alkoxy-Ci-Cg-alkyl, C 1 -C 1 O-AUCyItIIiO-C 1 - C 6 -C 9 -cycloalkyl, optionally substituted by halogen, C 1 -C 6 -alkyl or C 1 -C 6 -alkenyl, in which one or two non-adjacent ring members are optionally replaced by oxygen and / or sulfur,
  • B is preferably hydrogen, C 1 -C] 2-alkyl or C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl or
  • A, B and the carbon atom to which they are attached preferably represent saturated C3-Ci Q cycloalkyl or unsaturated C5-C 1 o-cycloalkyl in which optionally one ring member is replaced by oxygen or sulfur and which is optionally monosubstituted or disubstituted by C -Cg-alkyl, C ⁇ Cg-haloalkyl or C] -Cg-alkoxy are substituted or
  • A, B and the carbon atom to which they are attached are preferably C 3 -C 6 -cycloalkyl which may optionally be replaced by an optionally one or two oxygen and / or sulfur atoms which are not directly adjacent to one another substituted alkylenediyl, or is substituted by an alkylenedioxy or by an alkylenedithioyl group which forms with the carbon atom to which it is bonded, another five- to eight-membered ring, or
  • A, B and the carbon atom to which they are attached are preferably C 3 -C 9 -cycloalkyl or C 5 -C 8 -cycloalkenyl in which two substituents together with the carbon atoms to which they are attached are in each case optionally denoted by C 1 - C 6 -alkyl, C 1 -C 6 -alkoxy or halogen-substituted C 2 -C 6 -alkanediyl, C 2 -C 6 -alkendiyl or C 1 -C 6 - Alkandiendiyl stand, wherein optionally a methylene group is replaced by oxygen or sulfur,
  • a and Q! together preferably represent in each case optionally monosubstituted or disubstituted, identically or differently, by halogen, hydroxyl, in each case optionally monosubstituted to trisubstituted by identical or different substituents, halogen-substituted C 1 -C 10 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkyl,
  • Q! and Q 2 independently of one another are preferably hydrogen or C 1 -C 4 -alkyl
  • X is preferably ethyl
  • Y is preferably methyl
  • A, B and the carbon atom to which they are attached are preferably saturated C 1 -C 6 -cycloalkyl or unsaturated C 1 -C 6 -cycloalkyl, in which optionally one Ring member is replaced by oxygen or sulfur and which are optionally mono- or disubstituted by Cj-Cg-alkyl, Cj-Cg-haloalkyl or Ci-Cg-alkoxy substituted, or
  • A, B and the carbon atom to which they are attached preferably represent C3 -Cg- cycloalkyl which is substituted by an optionally "means one or two not directly adjacent oxygen and / or sulfur atoms containing optionally substituted by C j -C ⁇ alkyl Alkylenediyl, or is substituted by an alkylenedioxy or by an alkylenedithioyl group which forms with the carbon atom to which it is bonded, another five- to eight-membered ring, or
  • A, B and the carbon atom to which they are attached are preferably C 3 -Cg-
  • Cycloalkyl or C5-C6cycloalkenyl in which two substituents together with the carbon atoms to which they are attached, are each substituted by C 1 -C 6 -alkyl, C 1 -C 8 -alkoxy or halogen-substituted C 2 -C 6 -alkanediyl, C 2 -C -g Alkenediyl or C 1 -C 6 -alkanediyl, in which optionally a methylene group is replaced by oxygen or sulfur,
  • Q! and Q ⁇ are preferably hydrogen, or
  • a and Q ' are together preferably in each case optionally mono- or di-identical, identical or different, by halogen, hydroxyl, in each case optionally monosubstituted to trisubstituted by identical or different halogens, C 1 -C -alkyl, C 1 -C -alkoxy, C 1 -cg-alkylthio, C3-C7-cycloalkyl or by in each case optionally mono- to trisubstituted by identical or different halogen, C j -Cg- alkyl or Cj-Cg-alkoxy-substituted benzyloxy or phenyl substituted C2-Cg alkanediyl or C2 Cg-alkenediyl, which also optionally one of the following groups
  • B and Q ⁇ independently of one another are preferably hydrogen or C1-C2-
  • G is preferably hydrogen (a) or one of the groups
  • E is a metal ion equivalent or an ammonium ion
  • M is oxygen or sulfur
  • R.1 preferably represents in each case optionally halogen-substituted C1-C20-
  • Alkyl C 2 -C 2 o-alkenyl, C 1 -Cg-alkoxy-Ci-C 8 -alkyl, C 1 -C 8 -AlkVItInO-C 1 -C 8 "alkyl, poly-C 1 -C 8 alkoxy C 1 -C 9 -alkyl or C 3 -C 9 -cycloalkyl optionally substituted by halogen, C 1 -CG -alkyl or C 1 -CG -alkoxy, in which if one or more (preferably not more than two) not directly adjacent ring members are replaced by oxygen and / or sulfur,
  • halogen is optionally substituted by halogen, cyano, nitro, C j -CG alkyl, Ci -CG-alkoxy, Ci - Coe haloalkyl, C j -CG-haloalkoxy, C j -CG-alkylthio, or C i--Cö Alkylsulfo- nyl substituted phenyl,
  • phenyl optionally substituted by halogen, nitro, cyano, C j -Cg-alkyl, Ci-Cö-alkoxy, Cj-Cg-haloalkyl or Cj-Cg-haloalkoxy-Cj-Cö-alkyl,
  • C j -Cg-alkyl-substituted 5- or 6-membered hetaryl for example, pyrazolyl, thiazolyl, pyridyl, pyrimidyl, furanyl or thienyl
  • halogen or C j -Cg-alkyl-substituted 5- or 6-membered hetaryl for example, pyrazolyl, thiazolyl, pyridyl, pyrimidyl, furanyl or thienyl
  • R 1 is preferably in each case halogen-substituted C 1 -C 20 -alkyl, C 2 -C 2 0-alkenyl, C 1 -C 6 -alkoxy-C 2 -C 6 -alkyl, poly-C 1 -C 6 -alkoxy-C 1 -C 4 -alkyl,
  • R ⁇ preferably represents optionally halogen-substituted C j -CG alkyl or in each case optionally substituted by halogen, Cj-Cg-alkyl, Ci -CG-alkoxy, C1-C4
  • Haloalkyl C j -C 4 -haloalkoxy, cyano or nitro-substituted phenyl or benzyl,
  • R ⁇ and R ⁇ are preferably independently of one another represent in each case optionally halogen-substituted Cj-Cg-alkyl, C j -CG-alkoxy, Ci -CG-alkylamino, di- (C j - Cg-alkyl) amino, C j -CG-alkylthio, C2-Cg-alkenylthio, C3-C7-cycloalkylthio or represent in each case optionally substituted by halogen, nitro, cyano, C j-C4-alkoxy, C1-C4-haloalkoxy, C] -C 4 alkylthio, C 1 -C 4 haloalkylthio, C 1 -C 4 alkyl or C 1 - C4 haloalkyl-substituted phenyl, phenoxy or phenylthio,
  • R.6 and R ⁇ are each independently preferably represents hydrogen, represents in each case optionally halogen-substituted C 1 -CG-AIlCyI, C3-Cg cycloalkyl, C 1 - Cg-alkoxy, C3-Cg-alkenyl, C ⁇ Cg alkoxy -C ⁇ Cg-alkyl, phenyl optionally substituted by halogen, C ⁇ Cg-haloalkyl, Ci-Cg-alkyl or C 1 -Cg-AIkOXy, optionally substituted by halogen, Cj-Cg-alkyl, Ci-Cg-haloalkyl or C 1 -C 6 -alkoxy-substituted benzyl or together for an optionally C 1 -CG-AIlCyI, C3-Cg cycloalkyl, C 1 - Cg-alkoxy, C3-Cg-alkenyl, C ⁇ Cg alkoxy
  • R! 3 is preferably hydrogen, in each case optionally substituted by halogen C 1 -Cg-AllCyI, C] -Cg-alkoxy or C3-Cg-alkenyloxy, optionally substituted by halogen, C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy substituted C3-
  • Cg-cycloalkyl in which optionally one methylene group is replaced by oxygen or sulfur, or represents in each case optionally halogen-, C 1 -Cg- alkyl, C] -CG-alkoxy, C1-C4-haloalkyl, Ci-C4-haloalkoxy, nitro or cyano-substituted phenyl, hetaryl, phenyl-C j-C4-alkyl, phenyl-C j-C4-alkoxy or hetaryl-Ci-C4-alkoxy,
  • R ⁇ a is preferably hydrogen or Ci-Cg-alkyl or
  • R * 3 and R ⁇ a together are preferably C4-C6-alkanediyl
  • R ⁇ a and R ⁇ a are the same or different and are preferably C j -Cg-alkyl or
  • R ⁇ a and Rl " a together are preferably a C2-C4-alkanediyl radical which is optionally substituted by Ci-Cg-alkyl, Ci-Cg-haloalkyl or by optionally halogen, C j -Cg-alkyl, Ci-C4-haloalkyl , C 1 -Cg -alkoxy, C 1 -C 4 -haloalkoxy, nitro or cyano-substituted phenyl,
  • Rl ⁇ a nd R ⁇ a are independently preferably represents hydrogen, represents optionally halogen-substituted Cj-Cg-alkyl, or represents optionally substituted by halogen, C ⁇ Cg alkyl, C 1 -CG-AUcOXy, C 1 -C 4 haloalkyl , C 1 -C 4 -haloalkoxy, nitro or cyano-substituted phenyl or R ⁇ a and R ⁇ a, together with the carbon atom to which they are attached, are preferably a carbonyl group or C5-C7-cycloalkyl optionally substituted by halogen, C1-C4-alkyl or C1-C4-alkoxy, in which, if appropriate a methylene group is replaced by oxygen or sulfur,
  • j R20a are each independently preferably C ⁇ -C ⁇ Q -alkyl, C2-CJQ-
  • halogen is fluorine, chlorine, bromine and iodine, in particular fluorine, chlorine and bromine.
  • X is particularly preferred for Mehyl
  • Y is particularly preferably methyl or ethyl
  • X and Y are both particularly preferably ethyl
  • B particularly preferably represents hydrogen, C 1 -C 4 -alkyl or C 1 -C 2 -alkoxy-C 1 -C 2 -alkyl or
  • A, B and the carbon atom to which they are attached are particularly preferably saturated or unsaturated C5-C7-cycloalkyl, in which optionally one ring member is replaced by oxygen or sulfur and which optionally mono- to disubstituted by Ci-Cg-alkyl, trifluoromethyl or C j -Cg alkoxy, substituted,
  • A, B and the carbon atom to which they are attached are particularly preferably C 5 -C 6 -cycloalkyl which is not directly adjacent to one or two by an optionally one or two
  • A, B and the carbon atom to which they are attached are particularly preferably C3-C6-
  • Q! and Q 1 independently of one another particularly preferably represent hydrogen or C 1 -C 2 -alkyl
  • X is particularly preferably ethyl
  • Y is particularly preferably methyl
  • A, B and the carbon atom to which they are attached particularly preferably represent saturated or unsaturated C5-C7-cycloalkyl in which optionally one ring member is replaced by oxygen or sulfur and which is optionally monosubstituted or disubstituted by C j -Cö alkyl , Trifluoromethyl or C j -Cg alkoxy is substituted with the proviso that then Q ⁇ is particularly preferably hydrogen or methyl, or
  • A, B and the carbon atom to which they are attached are particularly preferably C5-C6-cycloalkyl which may be replaced by an optionally one or two non-directly adjacent oxygen or sulfur atoms
  • A, B and the carbon atom to which they are attached are particularly preferably
  • Q * and Q ⁇ are particularly preferably hydrogen
  • a and Q * together are particularly preferably together in each case optionally mono- or disubstituted by identical or different hydroxy, C 1 -C 2 -alkyl or C 1 -C 4 -alkoxy-substituted C 3 -C 4 -alkanediyl, or C 3 -C 4 -alkendiyl, which is optionally a of the following groups
  • B and Q ⁇ independently of one another particularly preferably represent hydrogen or methyl
  • G is particularly preferably hydrogen (a) or one of the groups
  • E is a metal ion equivalent or an ammonium ion
  • M is oxygen or sulfur
  • R.1 particularly preferably represents in each case optionally mono- to trisubstituted by fluorine or chlorine, C 1 -C 6 -alkyl, C 2 -C -alkenyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl,
  • C2-alkyl or optionally mono- to disubstituted by fluorine, chlorine, C j -C 2 -alkyl or C 1 -C 2 -alkoxy-substituted C 3 -C 6 -cycloalkyl in which optionally one or two non-directly adjacent ring members are replaced by oxygen,
  • Ci-C4-alkyl C j ⁇ -C alkoxy, Ci-C2-haloalkyl or Ci-C2-haloalkoxy-substituted phenyl,
  • R ⁇ particularly preferably represents in each case optionally mono- to trisubstituted by fluorine -CG C j-alkyl, C2-Cg alkenyl, or Ci-C4-alkoxy-C2-C4-alkyl,
  • R ⁇ is particularly preferably optionally monosubstituted mono- to trisubstituted by fluorine Ci-Cg-alkyl, or represents optionally substituted by fluorine, chlorine, bromine, Ci-C4 alkyl, Cj-C4 alkoxy, trifluoromethyl, trifluoromethoxy, cyano or nitro phenyl,
  • R 1 particularly preferably represents in each case optionally monosubstituted to trisubstituted by fluorine or chlorine, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 8 -alkylamino,
  • R 5 particularly preferably represents optionally monosubstituted by chlorine Q-C ⁇ -alkoxy or C r C 6 -alkylthio,
  • R 1 particularly preferably represents hydrogen, C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl, C 1 -C 4 -alkyl,
  • Ci -CG-alkoxy-Ci-C ⁇ alkyl which is optionally monosubstituted by fluorine, chlorine, bromine, trifluoromethyl, C j -C zj alkyl or Ci-C4-alkoxy-substituted Phenyl, optionally substituted by fluorine, chlorine, bromine, C1-C4
  • R 1 particularly preferably represents Q-C 1 -alkyl, C 3 -C 6 -alkenyl or C 1 -C 6 -alkoxy-C 1 -C 4 -alkyl,
  • R "and R 'particularly preferably together represent an optionally substituted by methyl or ethyl C 4 -C 5 -alkylene radical in which optionally a methylene group is replaced by oxygen or sulfur,
  • R! 3 particularly preferably represents hydrogen, in each case optionally mono- to trisubstituted by fluorine or chlorine, C j -Cg-alkyl, C j -Cg alkoxy, C 3 -Cg alkenyloxy optionally substituted by halogen, C j -C ⁇ alkyl or Ci -C ⁇ alkoxy-substituted C3-Cg-cycloalkyl in which optionally one methylene group is replaced by oxygen or sulfur, or represents in each case optionally substituted by fluorine, chlorine, bromine, Cj-C ⁇ alkyl, C j ⁇ alkoxy, Ci-C2- haloalkyl, C1-C2 haloalkoxy, nitro or cyano-substituted phenyl, pyridyl, pyrimidyl, thiazolyl, phenyl-C j -C 2 alkyl or pyridyl-C j -C
  • R 1 a and R 1 a independently of one another particularly preferably represent hydrogen, for C 1 -C 4 -cycloalkyl optionally substituted once to three times by fluorine or chlorine
  • Alkyl or optionally once or twice by fluorine, chlorine, bromine,
  • R ⁇ a and R ⁇ a together with the carbon atom to which they are attached, are particularly preferably a carbonyl group or C5-C6 which is optionally mono- to disubstituted by fluorine, chlorine, C 1 -C 3 -alkyl or C 1 -C 4 -alkoxy cycloalkyl.
  • halogen is fluorine, chlorine and bromine, in particular fluorine and chlorine.
  • X is most preferably methyl
  • Y very particularly preferably represents methyl or ethyl
  • X and Y are most preferably ethyl
  • A is very particularly preferably hydrogen, in each case optionally mono- to trisubstituted by fluorine-substituted C 1 -C 4 -alkyl or C 1 -C 2 -alkoxy-C 1 -C 2 -alkyl, for cyclopropyl, cyclopentyl or cyclohexyl,
  • B is very particularly preferably hydrogen, methyl or ethyl or
  • A, B and the carbon atom to which they are attached very particularly preferably represent saturated C 5 -C 6 -cycloalkyl in which optionally a ring member is replaced by oxygen and which is optionally substituted by methyl, ethyl, propyl, isopropyl, trifluoromethyl, methoxy, Ethoxy, propoxy or butoxy is substituted,
  • A, B and the carbon atom to which they are attached are very particularly preferably C 9 -cycloalkyl which is substituted by alkylenedioxyl groups containing two non-directly adjacent oxygen atoms which are bonded to the carbon atom to which it is attached. forms another five- or six-membered ring,
  • A, B and the carbon atom to which they are attached are most preferably C5-C6 cycloalkyl or C5-C6 cycloalkenyl wherein two substituents together with the carbon atoms to which they are attached are C2-C4 alkanediyl or C2-C4-alkenediyl or butadienediyl,
  • a and Q! together are very particularly preferably together in each case optionally monosubstituted or disubstituted by identical or different hydroxy, methyl or methoxy-substituted C3-C4 "alkanediyl or C3-C4-alkenediyl
  • Q! and Q 1 independently of one another very particularly preferably represent hydrogen or methyl
  • X is most preferably ethyl
  • Y is very particularly preferably methyl
  • A, B and the carbon atom to which they are attached very particularly preferably represent saturated C 5 -C 6 -cycloalkyl in which optionally a ring member is replaced by oxygen or sulfur and which is optionally monosubstituted by methyl, ethyl, propyl, isopropyl, Trifluoromethyl, methoxy, ethoxy, propoxy or
  • A, B and the carbon atom to which they are attached most preferably represent C 6 -cycloalkyl substituted by an alkylenedioxy group containing two non-directly adjacent oxygen atoms attached to the carbon to which it is attached, another five forms - or six-membered ring,
  • A, B and the carbon atom to which they are attached are very particularly preferably C5-C6-cycloalkyl or C5-C ( C-cycloalkenyl, in which two substituents, together with the carbon atoms to which they are bonded, represent C2 C4-alkanediyl or C2-C4-alkenediyl or butadienediyl,
  • Q! and Q ⁇ are most preferably hydrogen
  • a and Q! together very particularly preferably represents in each case optionally mono- or disubstituted by hydroxy, methyl or methoxy-substituted C3-C4-alkanediyl or C3-C4-alkenediyl
  • B and Q ⁇ very particularly preferably independently of one another represent hydrogen or methyl
  • G is very particularly preferably hydrogen (a) or one of the groups
  • E is an ammonium ion
  • M is oxygen or sulfur
  • R.1 very particularly preferably represents C j -Cg-alkyl, C 2 -C 6 -alkenyl, C 1 -C 2 -alkoxy-C 1 -alkyl, C 1 -C 2 -alkylthio-C 1 -alkyl or optionally simply by fluorine, chlorine, methyl or methoxy-substituted C3-Cg-cyclopropyl or monosubstituted by chlorine C] -C ⁇ alkyl,
  • R.2 very particularly preferably represents in each case optionally mono- to trisubstituted fluorine-substituted C j -Cg-alkyl, C 2 -C 6 -alkenyl or C 1 -C 4 -alkoxy-C 2 -C 3 -alkyl, phenyl or benzyl,
  • R.3 very particularly preferably represents C 1 -C -alkyl
  • R ⁇ is very particularly preferably represents in each case optionally mono- to trisubstituted by fluorine or chlorine, Cj-C ⁇ alkyl, Ci-C4 alkoxy, Cj-C4 alkylamino, di- (C i-C4-alkyl) amino, Ci C4-alkylthio, C3-C4-alkenylthio, C3-Cg-Cyc loalkylthio or represents in each case optionally monosubstituted by fluorine, chlorine, bromine, nitro, cyano, methoxy, trifluoromethoxy, methylthio, trifluoromethylthio, methyl or trifluoromethyl, phenyl, phenoxy or phenylthio,
  • R ⁇ is very particularly preferably optionally monosubstituted by chlorine C, -C 4 alkoxy or Ci-C 4 alkylthio,
  • R.13 very particularly preferably represents in each case optionally mono- to trisubstituted by fluorine or chlorine, C j -C ⁇ alkyl, Ci-C / j alkoxy or C3-C4 alkenyloxy or represents in each case optionally substituted by fluorine, chlorine, bromine, methyl , Methoxy, trifluoromethyl or trifluoromethoxy substituted benzyl or pyridyl,
  • R.sup.1a and R.sup.a are very particularly preferably C 1 -C 4 -alkyl which is optionally monosubstituted to trisubstituted by fluorine or chlorine, or optionally monosubstituted or disubstituted by fluorine, chlorine, bromine, methyl, methoxy, trifluoromethyl, trifluoromethoxy, nitro or cyano substituted phenyl or
  • R! ' a and R' ° a together with the carbon atom to which they are attached are very particularly preferably C5-C6-cycloalkyl which is optionally monosubstituted or disubstituted by methyl or ethyl.
  • Y stands for methyl or ethyl
  • X and Y are both ethyl
  • A stands for methyl
  • B is hydrogen or methyl
  • A, B and the carbon atom to which they are attached stand for saturated C5-C6-cycloalkyl in which optionally a ring member is replaced by oxygen and which is optionally substituted by methyl,
  • a and Q! together are each C3-C5-alkanediyl or C3-C5-alkenediyl, which is optionally monosubstituted by methyl, which optionally contain one of the following groups
  • a and Q! together are each C3-C5-alkanediyl or C3-C5-alkenediyl, which is optionally monosubstituted by methyl,
  • G is hydrogen (a) or one of the groups
  • R.1 represents C ⁇ -CG alkyl, C j-C2-alkoxy-Ci-C2-alkyl, or for single-chlorine-substituted C j ⁇ -C alkyl,
  • R 2 stands for C j -Cg-alkyl
  • R 1 stands for C 1 -C 4 -alkoxy, which is optionally monosubstituted by chlorine,
  • R ⁇ stands for C1-C4, which is optionally monosubstituted by chlorine.
  • R ⁇ a and R ⁇ a stand for methyl.
  • X and Y independently of one another represent methyl or ethyl
  • trans compounds being particularly emphasized.
  • the general or preferred radical definitions or explanations given above can be combined as desired with one another, ie also between the respective ranges and preferred ranges. They apply accordingly to the end products as well as to the precursors and intermediates.
  • Saturated or unsaturated hydrocarbon radicals such as alkyl, alkanediyl or alkenyl, may also be used in conjunction with heteroatoms, e.g. in alkoxy, as far as possible, in each case straight-chain or branched.
  • Optionally substituted radicals may, unless stated otherwise, be monosubstituted or polysubstituted, with multiple substitutions the substituents being the same or different.
  • m is preferably the numbers O, 1, 2, 3 or 4.
  • a 1 preferably represents one of the divalent heterocyclic groupings outlined below
  • n preferably represents the numbers 0, 1, 2, 3 or 4.
  • a 2 preferably represents in each case optionally methyl, ethyl, methoxycarbonyl or ethoxycarbonyl-substituted methylene or ethylene.
  • R 14 is preferably hydroxy, mercapto, amino, methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylthio, ethylthio, n- or i-propylthio, n-, i -, s- or t-butylthio, methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, dimethylamino or diethylamino.
  • R ⁇ is preferably hydroxy, mercapto, amino, methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, 1-methylhexyloxy, allyloxy, 1-allyloxymethyl-ethoxy, methylthio, ethylthio , n- or i-Propylthio, n-, i-, s- or t-butylthio, methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, dimethylamino or diethylamino.
  • R 16 is preferably in each case optionally substituted by fluorine, chlorine and / or bromine substituted methyl, ethyl, n- or i-propyl.
  • R 1 ⁇ is preferably hydrogen, in each case optionally substituted by fluorine and / or chlorine
  • R 18 is preferably hydrogen, in each case optionally fluorine- and / or chlorine-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, propenyl, butenyl, propynyl or butynyl, methoxymethyl, Ethoxymethyl, MeÜioxyethyl, ethoxyethyl, dioxolanylmethyl, furyl, furyl methyl, thienyl, thiazolyl, piperidinyl, or optionally by fluorine, chlorine, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl substituted phenyl, or R 17 and R 18 are also together one of the radicals -CH 2 -O-CH 2 -CH 2 - and -CH 2 -CH 2 -O-CH 2 -CH
  • R 19 preferably represents hydrogen, cyano, fluorine, chlorine, bromine, or represents in each case optionally substituted by fluorine, chlorine and / or bromine substituted methyl, ethyl, n- or i-propyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or phenyl.
  • R 20 is preferably hydrogen, optionally substituted by hydroxyl, cyano, fluorine, chlorine, methoxy, ethoxy, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t- butyl.
  • R 21 preferably represents hydrogen, cyano, fluorine, chlorine, bromine, or represents in each case optionally fluorine, chlorine and / or bromine-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t- Butyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or phenyl.
  • X 1 is preferably nitro, cyano, fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, difluoromethyl, dichloromethyl, trifluoromethyl, trichloromethyl, chlorodifluoromethyl, fluorodichloromethyl , Methoxy, ethoxy, n- or i-propoxy, difluoromethoxy or trifluoromethoxy.
  • X 2 is preferably hydrogen, nitro, cyano, fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, difluoromethyl, dichloromethyl, trifluoromethyl, trichloromethyl, chlorodifluoromethyl , Fluorodichloromethyl, methoxy, ethoxy, n- or i-propoxy, difluoromethoxy or trifluoromethoxy.
  • X 3 is preferably hydrogen, nitro, cyano, fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, difluoromethyl, dichloromethyl, trifluoromethyl, trichloromethyl, chlorodifluoromethyl , Fluorodichloromethyl, methoxy, ethoxy, n- or i-propoxy, difluoromethoxy or trifluoromethoxy.
  • t preferably stands for the numbers 0, 1, 2, 3 or 4.
  • v preferably represents the numbers 0, 1, 2, 3 or 4.
  • R 22 is preferably hydrogen, methyl, ethyl, n- or i-propyl.
  • R 23 is preferably hydrogen, methyl, ethyl, n- or i-propyl.
  • R 24 is preferably hydrogen, in each case optionally cyano, fluorine, chlorine, methoxy, ethoxy, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl .
  • R 25 is preferably hydrogen, in each case optionally cyano, hydroxyl, fluorine, chlorine, methoxy, ethoxy, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, each optionally substituted by cyano, fluorine, chlorine or bromine Pr ⁇ penyl,
  • R 26 is preferably hydrogen, in each case optionally cyano, hydroxyl, fluorine, chlorine, methoxy, ethoxy, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-
  • X 4 is preferably nitro, cyano, carboxy, carbamoyl, formyl, sulfamoyl, hydroxy, amino, fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl , Trifluoromethyl, " methoxy, ethoxy, n- or i-propoxy, difluoromethoxy or trifluoromethoxy.
  • X 5 is preferably nitro, cyano, carboxy, carbamoyl, formyl, sulfamoyl, hydroxy, amino, fluorine, chlorine, bromine, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl , Trifluoromethyl, methoxy, ethoxy, n- or i-propoxy, difluoromethoxy or trifluoromethoxy.
  • herbicidal safeners particularly preferred compounds of the formula (Ha) according to the invention are listed in the table below.
  • herbicidal safeners particularly preferred compounds of formula (Ub) according to the invention are listed in the table below.
  • herbicidal safeners according to the invention very particularly preferred compounds of the formula (TIe) are listed in the table below.
  • crop plant compatibility-improving compound [component (b ')] are cloquintocetmexyl, fenchlorazole-ethyl, isoxadifen-ethyl, mefenpyr-diethyl, furilazoles, fenclorim, cumylurin, dymron, dimepiperate and the compounds IIe-5 and IIe 11 are most preferred, with cloquintocetmexyl and mefenpyr-diethyl being particularly emphasized.
  • the compounds of the general formula (IIa) to be used according to the invention as safeners are known and / or can be prepared by processes known per se (cf., WO-A-91/07874, WO-A-95/07897).
  • the compounds of general formula (IId) which are to be used according to the invention as safeners are known and / or can be prepared by processes known per se (cf., DE-A-19621522 / US-A-6235680).
  • the compounds of the general formula (IIe) which are to be used according to the invention as safeners are known and / or can be prepared by processes known per se (cf., WO-A-99/66795 / US-A-6251827).
  • reaction can be characterized by the following Reaction scheme to be reproduced:
  • A, B, Q! , Q 2 , X, Y and R 8 are as defined above,
  • the 5-aryl-4-ketocarboxylic acid esters of the formula (II) are obtained, for example, by reacting 5-aryl-4-ketocarboxylic acids of the formula (XIII)
  • X, Y, A, B, Q * and Q 2 are as defined above,
  • the 5-aryl-4-ketocarboxylic acids of the formula (XIII) are obtained, for example, by reacting 2-phenyl-3-oxo-adipic esters of the formula (XFV)
  • A, B, Ql, Q 2 , X and Y are as defined above and
  • R 8 and R 8 ' are alkyl (especially Ci-Cg-alkyl) and
  • A, B, Ql, Q 2 and R 8 are as defined above and
  • Hal is chlorine or bromine
  • the compounds of the formulas (XV) and (XVI) are partially known compounds of organic chemistry and / or can be prepared in a simple manner by methods known in principle.
  • acid halides of the formula (III), carboxylic acid anhydrides of the formula (W) , Chloroformates or chloroformic thioesters of the formula (V), Chlormonothioameisen Anlagenreester or Chlordithioameisen Acidester of formula (VT), sulfonic acid chlorides of the formula (VII), phosphorus compounds of the formula (VIII) and metal hydroxides, metal alkoxides or amines of the formula (IX) and (X) and Isocyanates of the formula (XI) and carbamic acid chlorides of the formula (XII) are generally known compounds of organic or inorganic chemistry.
  • the process (A) is characterized by subjecting compounds of the formula (II) in which A, B, Q.sup.1, Q.sup.1, X, Y and R.sup.1 have the abovementioned meaning to an intramolecular condensation in the presence of a base.
  • Suitable diluents in process (A) according to the invention are all organic solvents which are inert to the reactants.
  • organic solvents which are inert to the reactants.
  • hydrocarbons such as toluene and xylene
  • ethers such as dibutyl ether, tetrahydrofuran, dioxane, glycol dimethyl ether and diglycol dimethyl ether
  • polar solvents such as dimethyl sulfoxide, sulfolane, dimethylformamide and N-methyl-pyrrolidone.
  • alcohols such as methanol, ethanol, propanol, isopropanol, butanol, isobutanol, tert-butanol can be used.
  • Suitable bases (deprotonating agents) when carrying out the process (A) according to the invention are all customary proton acceptors.
  • Preferably used are alkali metal and alkaline earth metal oxides, hydroxides and carbonates, such as sodium hydroxide, potassium hydroxide, magnesium oxide, calcium oxide, sodium carbonate, potassium carbonate and calcium carbonate, which are also useful in the presence of phase transfer catalysts, e.g. Triethylbenzylammonium chloride, molar amounts.
  • phase transfer catalysts e.g. Triethylbenzylammonium chloride, molar amounts.
  • the process (B- ⁇ ) is characterized in that compounds of the formula (I-a) are each reacted with carboxylic acid halides of the formula (III), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.
  • Suitable diluents for the process (B- ⁇ ) according to the invention are all solvents which are inert to the acid halides. Preference is given to using hydrocarbons, such as benzene, benzene, toluene, xylene and tetralin, furthermore halogenated hydrocarbons, such as methylene chloride, chloroform, carbon tetrachloride, chlorobenzene and o-dichlorobenzene, furthermore ketones, such as acetone and methyl isopropyl ketone, furthermore ethers, such as diethyl ether, tetrahydrofuran and dioxane, in addition, carboxylic acid esters, such as ethyl acetate, and also highly polar solvents, such as dimethyl sulfoxide and sulfolane. If the hydrolytic stability of the acid halide permits it, the reaction may also be carried out in the presence of water.
  • hydrocarbons such
  • Suitable acid binders in the reaction by the process (B- ⁇ ) according to the invention are all customary acid acceptors.
  • tertiary amines such as triethylamine, pyridine, diazabicyclooctane (DABCO), diazabicycloundecene (DBU), diazabicyclo-nonene (DBN), Hünig base and N,
  • the reaction temperatures can be varied within a relatively wide range in the process (B- ⁇ ) according to the invention. In general, one works at temperatures between -20 0 C and +150 0 C, preferably between 0 0 C and 100 0 C.
  • the starting materials of the formula (Ia) and the carboxylic acid halide of the formula (III) are generally each used in approximately equivalent amounts. However, it is also possible to use the carboxylic acid halide in a larger excess (up to 5 moles). The workup is carried out by conventional methods.
  • the process (B- ⁇ ) is characterized in that compounds of the formula (I-a) are reacted with carboxylic anhydrides of the formula (TV), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.
  • Diluents which may be used in the process (B- ⁇ ) according to the invention are preferably those diluents which are also preferred when using acid halides.
  • an excess carboxylic acid anhydride may also function as a diluent at the same time.
  • Suitable acid binders which may be added in the process (B- ⁇ ) are preferably those acid binders which are also preferably used when acid halides are used.
  • reaction temperatures can be varied within a relatively wide range in the process (B- ⁇ ) according to the invention. In general, one works at temperatures between -20 0 C and +150 0 C, preferably between 0 0 C and 100 0 C.
  • the starting materials of the formula (I-a) and the carboxylic anhydride of the formula (TV) are generally used in respectively approximately equivalent amounts.
  • the carboxylic acid anhydride in a larger excess (up to 5 moles).
  • the workup is carried out by conventional methods.
  • diluent and excess carboxylic anhydride and the resulting carboxylic acid are removed by distillation or by washing with an organic solvent or with water.
  • the process (C) is characterized in that compounds of the formula (I-a) are reacted in each case with chloroformates or chloroformic thioesters of the formula (V), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.
  • Suitable acid binders in the reaction according to the process (C) according to the invention are all customary acid acceptors.
  • Suitable diluents for the process (C) according to the invention are all solvents which are inert to the chloroformic esters or chloroformic thioesters.
  • hydrocarbons such as benzene, benzene, toluene, xylene and tetralin
  • halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, chlorobenzene and o-dichlorobenzene
  • ketones such as acetone and methyl isopropyl ketone
  • furthermore ethers such as diethyl ether, tetrahydrofuran and Dioxane
  • carboxylic acid esters such as ethyl acetate
  • strongly polar solvents such as dimethyl sulfoxide and sulfolane.
  • reaction temperatures can be varied within a relatively wide range.
  • the reaction temperatures are generally between - 20 0 C and + 100 0 C, preferably between 0 0 C and 50 0 C.
  • the process (C) according to the invention is generally carried out under atmospheric pressure.
  • the starting materials of the formula (I-a) and the corresponding chloroformate or chloroformic thioester of the formula (III) are generally used in approximately equivalent amounts. However, it is also possible to use one or the other component in a larger excess (up to 2 mol).
  • the workup is carried out by conventional methods. In general, the procedure is to remove precipitated salts and to narrow the remaining reaction mixture by stripping off the diluent.
  • the process (D) according to the invention is characterized in that compounds of the formula (I-a) are each reacted with compounds of the formula (VI) in the presence of a diluent and if appropriate in the presence of an acid binder.
  • Suitable optionally added diluents are all inert polar organic solvents, such as ethers, amides, sulfones, sulfoxides, but also haloalkanes. Preference is given to using dimethyl sulfoxide, tetrahydrofuran, dimethylformamide or methylene chloride.
  • the addition of strong deprotonating agents e.g. Sodium hydride or potassium tert-butylate is the enolate salt of the compounds (I-a), can be dispensed with the further addition of acid binders.
  • customary inorganic or organic bases are suitable, for example sodium hydroxide, sodium carbonate, potassium carbonate, pyridine, triethylamine.
  • the reaction can be carried out at atmospheric pressure or under elevated pressure, preferably is carried out at atmospheric pressure.
  • the workup is done by conventional methods.
  • the process (E) according to the invention is characterized in that compounds of the formula (I-a) are each reacted with sulfonyl chlorides of the formula (VII), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.
  • Possible diluents which are added are all inert polar organic solvents, such as ethers, amides, nitriles, sulfones, sulfoxides or halogenated hydrocarbons, such as methylene chloride.
  • the addition of strong deprotonating agents represents the enolate salt of the compounds (I-a)
  • the further addition of acid binders can be dispensed with.
  • customary inorganic or organic bases are suitable, for example sodium hydroxide, sodium carbonate, potassium carbonate, pyridine, triethylamine.
  • the reaction can be carried out at atmospheric pressure or under elevated pressure, preferably is carried out at atmospheric pressure.
  • the workup is done by conventional methods.
  • the process (F) according to the invention is characterized in that compounds of the formula (Ia) are reacted in each case with phosphorus compounds of the formula (VIII), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.
  • Optionally added diluents are all inert, polar organic solvents such as ethers, amides, nitriles, alcohols, sulfides, sulfones, sulfoxides, etc.
  • acetonitrile dimethyl sulfoxide, tetrahydrofuran, dimethylformamide, methylene chloride are used.
  • Suitable acid binders which may be added are customary inorganic or organic bases such as hydroxides, carbonates or amines. Examples include sodium hydroxide, sodium carbonate, potassium carbonate, pyridine, triethylamine listed.
  • the reaction can be carried out at atmospheric pressure or under elevated pressure, preferably at atmospheric pressure.
  • the workup is done by conventional methods of organic chemistry.
  • the purification of the resulting end products is preferably carried out by crystallization, chromatographic purification or by so-called “undistillation", i. Removal of volatiles in vacuo.
  • the process (G) is characterized in that compounds of the formula (Ia) are reacted with metal hydroxides or metal alkoxides of the formula (IX) or amines of the formula (X) 3, if appropriate in the presence of a diluent.
  • Suitable diluents in the process (G) according to the invention are preferably ethers such as tetrahydrofuran, dioxane, diethyl ether or else alcohols such as methanol, ethanol, isopropanol, but also water.
  • the process (G) according to the invention is generally carried out under atmospheric pressure.
  • the reaction temperatures are generally between -20 0 C and 100 0 C, preferably between 0 0 C and 5O 0 C.
  • the process (H) according to the invention is characterized in that compounds of the formula (Ia) are each reacted with (H- ⁇ ) compounds of the formula (XI), if appropriate in the presence of a Diluent and optionally in the presence of a catalyst or (H-ß) with compounds of formula (XII) optionally in the presence of a diluent and optionally in the presence of an acid binder.
  • Suitable diluents added are all inert organic solvents, such as ethers, amides, nitriles, sulfones, sulfoxides.
  • catalysts can be added to accelerate the reaction.
  • organotin compounds e.g. Dibutyltin dilaurate can be used. It is preferably carried out at atmospheric pressure.
  • Suitable diluents added are all inert polar organic solvents such as ethers, amides, sulfones, sulfoxides or halogenated hydrocarbons.
  • the enolate salt of compound (I-a) can be dispensed with, the further addition of acid binders.
  • strong deprotonating agents such as sodium hydride or potassium tertiary butylate
  • customary inorganic or organic bases are suitable, for example sodium hydroxide, sodium carbonate, potassium carbonate, triethylamine or pyridine.
  • the reaction can be carried out at atmospheric pressure or under elevated pressure, preferably is carried out at atmospheric pressure.
  • the workup is done by conventional methods.
  • the active compounds according to the invention are suitable for plant tolerance, favorable warm-blood toxicity and good environmental compatibility for the protection of plants and plant organs, for increasing crop yields, improving the quality of the crop and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and molluscs used in agriculture, horticulture, animal husbandry, forests, gardens and Adventureal facilities, in the storage and material protection and on the hygiene sector occur. They can preferably be used as crop protection agents. They are effective against normally sensitive and resistant species as well as against all or individual stages of development.
  • the above mentioned pests include:
  • Anoplura e.g. Damalinia spp., Haematopinus spp., Linognathus spp., Pediculus spp., Trichodectes spp.
  • arachnids e.g. Acarus siro, Aceria sheldoni, Aculops spp., Acutus spp., Amblyomma spp., Argas spp., Boophilus spp., Brevipalpus spp., Bryobia praetiosa, Chorioptes spp., Dermanyssus gallinae, Eotetranychus spp., Epitrimerus pyri, Eutetranychus spp.
  • Eriophyes spp. Hemitarsonemus spp., Hyalomma spp., Ixodes spp., Latrodectus mactans, Metatetranychus spp., Oligonychus spp., Ornithodoros spp., Panonychus spp., Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes spp., Rhipicephalus spp. Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus, Stenotarsonemus spp., Tarsonemus spp., Tetranychus spp., Vasates lycopersici.
  • Ceuthorhynchus spp. Ceuthorhynchus spp., Cleonus mendicus, Conoderus spp., Cosmopolites spp., Costelytra zealandica, Curculio spp., Cryptorhynchus lapathi, Dermestes spp., Diabrotica spp., Epilachna spp., Faustinus cubae, Gibbium psylloides, Heteronychus arator, Hylamorpha elegans, Hylotrupes bajulus, Hypera postica, Hypothenemus spp., Lachnosterna consanguinea, Leptinotarsa decemlineata, Lissorhoptrus oryzophilus, Lixus spp., Lyctus spp., Meligethes aeneus, Melolontha melolontha, Migdolus spp., Mono
  • Gastropoda e.g. Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Succinea spp.
  • helminths e.g. Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Brugia malayi, Brugia timori, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp., Dicrocoelium spp, Dictyocaulus filaria, Diphyllobothrium latum , Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp., Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa Loa, Ne
  • protozoa such as Eimeria
  • Eimeria protozoa
  • Heliopeltis spp. Horcias nobilellus, Leptocorisa spp., Leptoglossus phyllopus, Lygus spp., Macropes excavatus, Miridae, Nezara spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., Psallus seriatus, Pseudacysta persea, Rhodnius spp. Sahlbergella singularis, Scotinophora spp., Stephanitis nashi, Tibraca spp., Triatoma spp.
  • Hymenoptera e.g. Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Vespa spp.
  • Lepidoptera From the order of Lepidoptera, for example, Acronicta major, Aedia leucomelas, Agrotis spp., Alabama argillacea, Anticarsia spp., Barathra brassicae, Bucculatrix thurberiella, Bupalus piniarius, Cacoecia podana, Capua reticulana, Carpocapsa pomonella, Cheimatobia brumata, Chilo spp., Choristoneura fumiferana , Clysia ambiguella, Cnaphalocerus spp., Earias insulana, Ephestia kuehniella, Euproctis chrysorrhoea, Euxoa spp., Feltia spp., Galleria mellonella, Helicovepha spp., Heliothis spp., Hofmannophila pseudospretella, Homon
  • siphonaptera e.g. Ceratophyllus spp., Xenopsylla cheopis.
  • Symphyla e.g. Scutigerella immaculata.
  • Thysanoptera e.g. Basothrips biformis, Enneothrips flavens, Frankliniella spp., Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., RMpiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamoni, Thrips spp.
  • Thysanura e.g. Lepisma saccharina.
  • the plant parasitic nematodes include e.g. Anguina spp., Aphelenchoides spp., Belonoaimus spp., Bursaphelenchus spp., Ditylenchus dipsaci, Globodera spp., Heliocotylenchus spp., Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus similis, Rotylenchus spp. Trichodorus spp., Tylenchorhynchus spp., Tylenchulus spp., Tylenchulus semipenetrans, Xiphinema spp.
  • Anguina spp. Aphelenchoides spp., Belonoaimus spp., Bursaphelenchus spp., Ditylenchus dipsaci, Globodera
  • the compounds according to the invention may optionally also be used in certain concentrations or application rates as herbicides, safeners, growth regulators or agents for improving plant properties, or as microbicides, for example as fungicides, antimycotics, bactericides, viricides (including anti-viral agents) or as anti-MLO agents ( Mycoplasma-like-organism) and RLO (Rickettsia-like-organism). If appropriate, they can also be used as intermediates or precursors for the synthesis of further active ingredients.
  • plants and parts of plants can be treated.
  • plants are understood as meaning all plants and plant populations, such as desired and undesired wild plants or crop plants (including naturally occurring crop plants).
  • Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant varieties which can or can not be protected by plant breeders' rights.
  • Plant parts are to be understood as meaning all aboveground and underground parts and organs of the plants, such as shoot, leaf, flower and root, by way of example leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds and roots, tubers and rhizomes.
  • crops also include crops as well as vegetative and generative propagation material, such as cuttings, tubers, rhizomes, cuttings and seeds.
  • the treatment according to the invention of the plants and plant parts with the active ingredients is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, e.g. by dipping, spraying, evaporating, atomizing, spreading, brushing, injecting and in propagating material, in particular in seeds, further by single or multilayer coating.
  • the active compounds can be converted into the customary formulations, such as solutions, emulsions, wettable powders, water- and oil-based suspensions, powders, dusts, pastes, soluble powders, soluble granules, scattering granules, suspension-emulsion concentrates, active substance-impregnated natural products, active ingredient impregnated synthetic materials, fertilizers and micro-encapsulants in polymeric materials.
  • customary formulations such as solutions, emulsions, wettable powders, water- and oil-based suspensions, powders, dusts, pastes, soluble powders, soluble granules, scattering granules, suspension-emulsion concentrates, active substance-impregnated natural products, active ingredient impregnated synthetic materials, fertilizers and micro-encapsulants in polymeric materials.
  • formulations are prepared in a known manner, e.g. by mixing the active compounds with extenders, ie liquid solvents and / or solid carriers, if appropriate using surface-active agents, ie emulsifiers and / or dispersants and / or foam-forming agents.
  • extenders ie liquid solvents and / or solid carriers
  • surface-active agents ie emulsifiers and / or dispersants and / or foam-forming agents.
  • Excipients which can be used are those which are suitable for imparting particular properties to the composition itself or to preparations derived therefrom (for example spray mixtures, seed dressing), such as certain technical properties and / or special biological properties
  • auxiliaries are: extenders, solvents and carriers.
  • polar and non-polar organic chemical liquids e.g. from the classes of aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), alcohols and polyols (which may also be substituted, etherified and / or esterified), ketones (such as acetone, cyclohexanone), Esters (including fats and oils) and (poly) ethers, simple and substituted amines, amides, lactams (such as N-alkylpyrrolidones) and lactones, sulfones and sulfoxides (such as dimethyl sulfoxide).
  • aromatic and non-aromatic hydrocarbons such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes
  • alcohols and polyols which may also be substituted, etherified and / or esterified
  • ketones such
  • organic solvents can also be used as auxiliary solvents.
  • Suitable liquid solvents are essentially: aromatics, such as xylene, toluene, or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, Alcohols such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethyl sulfoxide, and water.
  • Suitable solid carriers are:
  • Ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as fumed silica, alumina and silicates, as solid carriers for granules are suitable: e.g. crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic flours and granules of organic material such as paper, sawdust, coconut shells, corn cobs and tobacco stalks; suitable emulsifiers and / or foam formers are: e.g.
  • nonionic and anionic emulsifiers such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, e.g. Alkylaryl polyglycol ethers, alkylsulfonates, alkyl sulfates, arylsulfonates and protein hydrolysates;
  • suitable dispersants are non-ionic and / or ionic substances, e.g.
  • Adhesives such as carboxymethylcellulose, natural and synthetic powdery, granular or latex-containing polymers such as gum arabic, polyvinyl alcohol, polyvinyl acetate, as well as natural phospholipids such as cephalins and lecithins and synthetic phospholipids may be used in the formulations.
  • Dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • inorganic pigments e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • additives may be fragrances, mineral or vegetable optionally modified oils, waxes and nutrients (also trace nutrients), such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • Stabilizers such as cold stabilizers, preservatives, antioxidants, light stabilizers or other chemical and / or physical stability-improving agents may also be present.
  • the formulations generally contain between 0.01 and 98% by weight of active ingredient, preferably between 0.5 and 90%.
  • the active ingredient according to the invention can be present in its commercial formulations and in the formulations prepared from these formulations in admixture with other active ingredients such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth-regulating substances, herbicides, safeners, fertilizers or semiochemicals.
  • active ingredients such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth-regulating substances, herbicides, safeners, fertilizers or semiochemicals.
  • Particularly favorable mixing partners are e.g. the following:
  • Azoxystrobin cyazofamide, dimoxystrobin, enestrobin, famoxadone, fenamidone, fluoxastrobin,
  • Carbamates for example alanycarb, aldicarb, aldoxycarb, allyxycarb, aminocarb, bendiocarb, benzuracarb, bufencarb, butacarb, butocarboxime, butoxycarboxime, carbaryl, carbofuran, carbosulfan, cloethocarb, dimetilane, ethiofencarb, fenobucarb, fenothiocarb,
  • Organophosphates for example acephates, azamethiphos, azinphos (-methyl, -ethyl), bromophos-ethyl, bromfenvinfos (-methyl), butathiofos, cadusafos, carbophenothione, chloroethoxyfos,
  • Chlorfenvinphos Chlormephos, Chlorpyrifos (-methyl / -ethyl), Coumaphos, Cyanofenphos, Cyanophos, Chlorfenvinphos, Demeton-S-methyl, Demeton-S-methylsulphone, Dialifos, Diacinone, Dichlofenthione, Dichlorvos / DDVP, Dicrotophos, Dimethoate, Dimethylvinphos , Dioxabenzofos, disulfone, EPN, Ethion, Ethoprophos, Etrimfos, Famphur, Fenamiphos, Fenitrothion, Fensulfothion, Fenthion, Flupyrazofos, Fonofos, Fo ⁇ nothion, Fosmethilan,
  • Fosthiazate Heptenophos, Iodofenphos, Iprobenfos, Isazofos, Isofenphos, Isopropyl O-salicylates, Isoxathion, Malathion, Mecarbam, Methacrifos, Methamidophos, Methidathion, Mevinphos, Monocrotophos, Naled, Omethoate, Oxydemeton-methyl, Parathion (-methyl / -ethyl), Phenthoate, Phorate, Phosalone, Phosmet, Phosphamidon, Phosphocarb, Phoxim, Pirimiphos (-methyl / -ethyl), Profenofos, Propaphos, Propetamphos, Prothiofos, Prothoate,
  • Pyrethroids for example, acrinathrin, allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, bioallethrin, bioallethrin-S-cyclopentyl isomer, bioethanomethrin, biopermethrin, bioresmethrin, chlovaporthrin, cis-cypermethrin, cis-resmethrin , Cis-permethrin, clocthrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin (alpha-, beta-, theta-, zeta-), cyphenothrin, deltamethrin, empenthrin (IR-isomer), esfenvalerate, etofenprox,
  • Chloronicotinyls for example acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazines,
  • Acetylcholine receptor modulators are Acetylcholine receptor modulators
  • Organochlorines for example, camphechlor, chlordane, endosulfan, gamma-HCH, HCH, heptachlor,
  • Fiproles for example, acetoprole, ethiprole, fipronil, pyrafluprole, pyriprole, vaniliprole
  • Mectins for example Abamectin, Emamectin, Emamectin benzoate, Ivermectin, Lepimectin, Milbemycin
  • Juvenile hormone mimetics for example, diofenolan, epofenonans, fenoxycarb, hydroprene, kinoprenes, methoprenes, pyriproxifen, triprene
  • Ecdysone agonists / disruptors Diacylhydrazines for example chromafenozide, Halofenozide, Methoxyfenozide, Tebufenozide
  • Benzoylureas for example bistrifluron, chlorofluazuron, diflubenzuron, fluazuron, flucycloxuron, fenphenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron, triflumuron
  • Organotin compounds for example azocyclotin, cyhexatin, fenbutatin oxides
  • Dinitrophenols for example binapacyrl, dinobutone, dinocap, DNOC, meptyldinocap
  • METI's for example Fenazaquin, Fenpyroximate, Pyrimidifen, Pyridaben, Tebufenpyrad, Tolfenpyrad
  • spirodiclofen for example spirodiclofen, spiromesifen,
  • anthranilamides for example, rynaxypyr (3-bromo-N- ⁇ 4-chloro-2-methyl-6- [(methylamino) carbonyl] phenyl ⁇ -1- (3-chloropyridin-2-yl) -1H-pyrazole-5-carboxamide )
  • Fumigants for example aluminum phosphides, methyl bromides, sulfuryl fluorides
  • Food inhibitors for example Cryolite, Flonicamid, Pymetrozine
  • Mite growth inhibitors for example clofentezine, etoxazole, hexythiazox
  • Gossyplure Hydramethylnone, Japonilure, Metoxadiazone, Petroleum, Piperonyl butoxide, Potassium oleate, Pyralidyl, Sulfluramide, Tetradifon, Tetrasul, Triarathene, Verbutin
  • a mixture with other known active substances, such as herbicides, fertilizers, growth regulators, safeners, semiochemicals, or with agents for improving the plant properties is possible.
  • the active compounds according to the invention can furthermore be present when used as insecticides in their commercial formulations and in the forms of use prepared from these formulations in admixture with synergists.
  • Synergists are compounds that increase the effect of the active ingredients without the added synergist itself having to be active.
  • the active compounds according to the invention may furthermore, when used as insecticides in their commercial formulations and in the forms of use prepared from these formulations, be present in mixtures with inhibitors which reduce degradation of the active ingredient after application in the environment of the plant, on the surface of plant parts or in plant tissues ,
  • the active substance content of the application forms prepared from the commercial formulations can vary within wide ranges.
  • the active ingredient concentration of the use forms may be from 0.00000001 up to 95% by weight of active compound, preferably between 0.00001 and 1% by weight.
  • the application is done in a custom forms adapted to the application.
  • plants and their parts can be treated.
  • wild species or plant species obtained by conventional biological breeding methods such as crossing or protoplast fusion
  • plant varieties and their parts are treated.
  • transgenic plants and plant cultivars which have been obtained by genetic engineering methods, if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated.
  • the terms "parts” or “parts of plants” or “plant parts” have been explained above.
  • Plant varieties are understood as meaning plants having new traits which have been bred by conventional breeding, by mutagenesis or by recombinant DNA techniques. These can be varieties, biotypes and genotypes.
  • the treatment according to the invention may also result in superadditive ("synergistic") effects.
  • superadditive for example, reduced application rates and / or enhancements of the activity spectrum and / or an increase in the effect of the substances and agents that can be used according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or against
  • the preferred plants or plant varieties to be treated according to the invention to be treated include all plants which, as a result of the genetic engineering modification, obtained genetic material which gives these plants particularly advantageous valuable properties ("traits").
  • traits are better plant growth, increased tolerance to high or low temperatures, increased tolerance to Dryness or against water or soil salt content, increased flowering efficiency, easier harvest, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products, higher shelf life and / or workability of the harvested products.
  • Further and particularly emphasized examples of such properties are an increased defense of the plants against animal and microbial pests, as against insects, mites, phytopathogenic fungi, bacteria and / or viruses as well as an increased tolerance of the plants against certain herbicidal active substances.
  • transgenic plants are the important crops such as cereals (wheat, rice), corn, soybeans, potatoes, sugar beets, tomatoes, peas and other vegetables, cotton, tobacco, oilseed rape and fruit plants (with the fruits apples, pears, citrus fruits and Grapes), with special emphasis on maize, soya, potato, cotton, tobacco and oilseed rape.
  • Bt plants are the increased defense of the plants against insects, arachnids, nematodes and snails by toxins produced in the plants, in particular those which are produced by the genetic material from Bacillus thuringiensis (eg by the genes Cry ⁇ A (a) , CryIA (b), Cry ⁇ A (c), CryllA, CrylllA, CryIIIB2, Cry9c Cry2Ab, Cry3Bb and CrylF, and combinations thereof) in the plants (hereinafter "Bt plants”).
  • Bacillus thuringiensis eg by the genes Cry ⁇ A (a) , CryIA (b), Cry ⁇ A (c), CryllA, CrylllA, CryIIIB2, Cry9c Cry2Ab, Cry3Bb and CrylF, and combinations thereof
  • Traits also highlight the increased resistance of plants to fungi, bacteria and viruses by systemic acquired resistance (SAR), systemin, phytoalexins, elicitors and resistance genes and correspondingly expressed proteins and toxins. Traits which are furthermore particularly emphasized are the increased tolerance of the plants to certain herbicidally active compounds, for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (eg "PAT" gene). The genes which confer the desired properties (“traits”) can also occur in combinations with one another in the transgenic plants.
  • SAR systemic acquired resistance
  • PAT phosphinotricin
  • Bt plants are maize varieties, cotton varieties, soybean varieties and potato varieties which are sold under the trade names YIELD GARD® (eg corn, cotton, soya), KnockOut® (eg maize), StarLink® (eg maize), Bollgard® ( Cotton), Nucotn® (cotton) and NewLeaf® (potato).
  • YIELD GARD® eg corn, cotton, soya
  • KnockOut® eg maize
  • StarLink® eg maize
  • Bollgard® Cotton
  • Nucotn® cotton
  • NewLeaf® potato
  • herbicide-tolerant plants are maize varieties, cotton varieties and soybean varieties, which are sold under the trade names Roundup Ready® (tolerance to glyphosate eg corn, cotton, soy), Liberty Link® (tolerance to phosphinotricin, eg rapeseed), IMI® (tolerance against imidazolinone) and STS® (tolerance to sulfonylureas eg corn).
  • Roundup Ready® tolerance to glyphosate eg corn, cotton, soy
  • Liberty Link® tolerance to phosphinotricin, eg rapeseed
  • IMI® tolerance against imidazolinone
  • STS® tolerance to sulfonylureas eg corn
  • Clearfield® varieties eg corn
  • the listed plants can be treated particularly advantageously according to the invention with the compounds of the general formula I or the active ingredient mixtures according to the invention.
  • the preferred ranges given above for the active compounds or mixtures also apply to the treatment of these plants.
  • Particularly emphasized is the plant treatment with the compounds or mixtures specifically mentioned in the present text.
  • the active compounds of the invention not only against plant, hygiene and storage pests, but also in the veterinary sector against animal parasites (ecto- and endoparasites) such as ticks, leather ticks, mange mites, running mites, flies (stinging and licking), parasitic fly larvae, lice , Hair pieces, featherlings and fleas.
  • animal parasites ecto- and endoparasites
  • ticks ecto- and endoparasites
  • leather ticks such as ticks, leather ticks, mange mites, running mites, flies (stinging and licking), parasitic fly larvae, lice , Hair pieces, featherlings and fleas.
  • flies stinging and licking
  • parasitic fly larvae such as ticks, leather ticks, mange mites, running mites, flies (stinging and licking), parasitic fly larvae, lice , Hair pieces, featherlings and fleas.
  • Anoplurida e.g. Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp.
  • Trimenopon spp. Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes spp., Felicola spp.
  • Nematocerina and Brachycerina e.g. Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp., Atylotus spp., Tabanus spp., Haematopota spp , Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Glossina spp., Chrysomyia spppp
  • siphonaptrida e.g. Pulex spp., Ctenocephalides spp., Xenopsylla spp., Ceratophyllus spp.
  • heteropterid e.g. Cimex spp., Triatoma spp., Rhodnius spp., Panstrongylus spp.
  • Actinedida Prostigmata
  • Acaridida e.g. Acarapis spp., Cheyletiella spp., Ornitrocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp., Pterolichus spp , Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp., Laminosioptes spp.
  • the active compounds of the formula (I) according to the invention are also suitable for controlling arthropods which are farm animals, such as e.g. Cattle, sheep, goats, horses, pigs, donkeys, camels, buffaloes, rabbits, chickens, turkeys, ducks, geese, bees, other pets such as e.g. Dogs, cats, caged birds, aquarium fish and so-called experimental animals, such. Hamsters, guinea pigs, rats and mice.
  • arthropods are farm animals, such as e.g. Cattle, sheep, goats, horses, pigs, donkeys, camels, buffaloes, rabbits, chickens, turkeys, ducks, geese, bees, other pets such as e.g. Dogs, cats, caged birds, aquarium fish and so-called experimental animals, such. Hamsters, guinea pigs, rats and mice.
  • the application of the active compounds according to the invention takes place in the veterinary sector and in animal husbandry in a known manner by enteral administration in the form of, for example, tablets, capsules, infusions, drenches, granules, pastes, boilies, the feed-through process, suppositories, by parenteral administration, as by injections (intramuscular, subcutaneous, intravenous, intraperitoneal, etc.), implants, by nasal application, by dermal application in the form of, for example, diving or bathing (dipping), spraying, pouring (pour-on and spot-on ), washing, powdering and with the aid of active substance-containing moldings, such as collars, ear tags, tail marks, limb bands, holsters, marking devices, etc.
  • enteral administration in the form of, for example, tablets, capsules, infusions, drenches, granules, pastes, boilies, the feed-through process, suppositories
  • parenteral administration as by injections (intr
  • the active compounds of the formula (I) can be used as formulations (for example powders, emulsions, flowable agents) which contain the active ingredients in an amount of from 1 to 80% by weight, directly or apply after 100 to 10,000 times dilution or use as a chemical bath.
  • formulations for example powders, emulsions, flowable agents
  • the compounds according to the invention have a high insecticidal activity against insects which destroy industrial materials.
  • insects By way of example and preferably without limiting however, the following insects are mentioned: Beetles such as Hylotrupes b Camillus, Chlorophorus pilosis, Anobium punctatum, Xestobium rufovillosum, Ptilinus pecticornis, Dendrobium pertinex, Ernobius mollis, Priobium carpini, Lyctus brunneus, Lyctus africanus, Lyctus planicollis, Lyctus linearis, Lyctus pubescens, Trogoxylon aequale, Minthes rugicollis, Xyleborus spec. Tryptodendron spec. Apate monachus, Bostrychus capucins, Heterobostrychus brunneus, Sinoxylon spec. Dinoderus minutus;
  • Hymenoptera such as Sirex juvencus, Urocerus gigas, Urocera gigas taignus, Urocerus augur;
  • Termites such as Kalotermes flavicollis, Cryptotermes brevis, Heterotermes indicola, Reticulitermes flavipes, Reticulitermes santonensis, Reticulitermes lucifugus, Mastotermes darwiniensis, Zootermopsis nevadensis, Coptotermes formosanus;
  • Non-living materials such as preferably plastics, adhesives, glues, papers and cardboard, leather, wood, wood processing products and paints.
  • the ready-to-use agents may optionally contain further insecticides and optionally one or more fungicides.
  • the compounds according to the invention can be used to protect against fouling of objects, in particular hulls, sieves, nets, structures, quay systems and signal systems, which come into contact with seawater or brackish water.
  • the compounds according to the invention can be used alone or in combinations with other active substances as antifouling agents.
  • the active compounds are also suitable for controlling animal pests in household, hygiene and storage protection, in particular of insects, arachnids and mites, which are used in closed rooms, such as apartments, factory buildings, offices, vehicle cabins u.a. occurrence. They can be used to control these pests, alone or in combination with other active ingredients and adjuvants in household insecticide products. They are effective against sensitive and resistant species and against all stages of development. These pests include:
  • Scorpionidea eg Buthus occitanus.
  • Acarina eg Argas persicus, Argas reflexus, Bryobia ssp., Dermanyssus gallinae, Glyciphagus domesticus, Ornithodorus moubat, Rhipicephalus sanguineus, Trombicula alfreddugesi, Neutrombicula autumnalis, Dermatophagoides pteronissimus, Dermatophagoides forinae.
  • Opiliones e.g. Pseudoscorpiones chelifer, Pseudoscorpiones cheiridium, Opiliones phalangium.
  • Zygentoma e.g. Ctenolepisma spp., Lepisma saccharina, Lepismodes inquilinus.
  • Ctenocephalides canis Ctenocephalides felis, Pulex irritans, Tunga penetrans, Xenopsylla cheopis.
  • Hymenoptera e.g. Camponotus herculeanus, Lasius fuliginosus, Lasius niger, Lasius umbratus, Monomorium pharaonis, Paravespula spp., Tetramorium caespitum.
  • Heteroptera e.g. Cimex hemipterus, Cimex lectularius, Rhodinus prolixus, Triatoma infestans.
  • Application is in aerosols, non-pressurized sprays, e.g. Pump and atomizer sprays, fog machines, foggers, foams, gels, evaporator products with cellulose or plastic evaporator plates, liquid evaporators, gel and membrane evaporators, propeller evaporators, energy-less or passive evaporation systems, moth papers, moth cushions and moth gels, as granules or dusts, in litter or bait stations.
  • Pump and atomizer sprays e.g. Pump and atomizer sprays, fog machines, foggers, foams, gels, evaporator products with cellulose or plastic evaporator plates, liquid evaporators, gel and membrane evaporators, propeller evaporators, energy-less or passive evaporation systems, moth papers, moth cushions and moth gels, as granules or dusts, in litter or bait stations.
  • the active compounds according to the invention can also be used as defoliants, desiccants, haulm killers and in particular as weed killers. Weeds in the broadest sense are all plants that grow in places where they are undesirable. Whether the substances according to the invention act as total or selective herbicides essentially depends on the amount used.
  • the active compounds of the invention may e.g. used in the following plants:
  • the active compounds according to the invention are suitable for total weed control, depending on the concentration, e.g. on industrial and railway tracks and on paths and squares with and without tree cover.
  • the active compounds of the present invention may be used for weed control in permanent crops, e.g. Forest, ornamental, fruit, wine, citrus, nut, banana, coffee, tea, gum, oil palm, cocoa, berry fruit and hop plants, on ornamental and sports lawns and pasture areas, and for selective weed control in annual crops.
  • the invention show strong herbicidal activity and a broad spectrum of activity when applied to the soil and on above-ground parts of plants. They are also to some extent also useful for the selective control of monocotyledonous and dicotyledonous weeds in monocotyledonous and cotyledonous crops, both preemergence and postemergence.
  • the active compounds according to the invention can also be used in certain concentrations or application rates for controlling animal pests and fungal or bacterial plant diseases. If appropriate, they can also be used as intermediates or precursors for the synthesis of further active ingredients.
  • the active compounds can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, dusts, pastes, soluble powders, granules, Suspension-emulsion concentrates, active substance-impregnated natural and synthetic substances as well as finest encapsulation in polymeric substances.
  • formulations are prepared in a known manner, for. Example, by mixing the active compounds with extenders, that is liquid solvents and / or solid carriers, optionally with the use of surfactants, emulsifiers and / or dispersants and / or foam-forming agents.
  • Suitable liquid solvents are essentially: aromatics, such as xylene, toluene, or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, e.g.
  • Petroleum fractions mineral and vegetable oils, alcohols such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
  • alcohols such as butanol or glycol and their ethers and esters
  • ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone
  • strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
  • Suitable solid carriers are: e.g. Ammonium salts and ground natural minerals, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as fumed silica, alumina and silicates, as solid carriers for granules are suitable: e.g. crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic flours and granules of organic material such as sawdust, coconut shells, corn cobs and tobacco stalks; suitable emulsifiers and / or foam formers are: e.g.
  • nonionic and anionic emulsifiers such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, e.g. Alkylaryl polyglycol ethers, alkylsulfonates, alkylsulfates, arylsulfonates and protein hydrolysates; suitable dispersants are: e.g. Lignin-sulphite liquors and methylcellulose.
  • Adhesives such as carboxymethyl cellulose, natural and synthetic powdery, granular or latex polymers such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids such as cephalins and lecithins and synthetic phospholipids may be used in the formulations.
  • Other additives may be mineral and vegetable oils.
  • Dyes such as inorganic pigments such as iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc can be used.
  • the formulations generally contain between 0.1 and 95% by weight of active ingredient, preferably between 0.5 and 90%.
  • the active compounds according to the invention can also be used in admixture with known herbicides and / or with substances which improve the crop plant compatibility ("safeners") for weed control, ready-to-use formulations or tank mixes being possible with weedkillers containing one or more known herbicides and a safener.
  • safeners substances which improve the crop plant compatibility
  • Acetochlor Acipped (-sodium), Aclonifen, Alachlor, Alloxydim (-sodium), Ametryne, Amicarbazone, Amidochlor, Amidosulfuron, Aminopyralid, Anilofos, Asulam, Atrazine, Azafenidine, Azim Sulfurone, Beflubutamide, Benazoline (-ethyl), Benfuresate, Bensulfuron (-methyl), Bentazone, Bencarbazone, Benzfendizone, Benzobicyclone, Benzofenap, Benzoylprop (-ethyl), Bialaphos, Bifen-ox, Bispyribac (-sodium), Bromobutide, Bromofenoxime, Bromoxynil, Butachlor, Butafenacil (-allyl), Butroxydim, butylates, cafenstrols, caloxydim, carbetamides, carfentrazone (-eth
  • a mixture with other known active ingredients such as fungicides, insecticides, acaricides, nematicides, bird repellants, plant nutrients and soil conditioners is also possible.
  • the active compounds or active compound combinations can be used as such, in the form of their formulations or the use forms prepared therefrom by further dilution, such as ready-to-use solutions, suspensions, emulsions, powders, pastes and granules.
  • the application is done in the usual way, e.g. by pouring, spraying, spraying, sprinkling.
  • the active compounds or active compound combinations according to the invention can be applied both before and after emergence of the plants. They can also be incorporated into the soil before sowing.
  • the amount of active ingredient used can vary within a substantial range. It depends essentially on the type of effect desired. In general, the application rates are between 1 g and 10 kg of active ingredient per hectare of soil, preferably between 5 g and 5 kg per ha.
  • the advantageous effect of the crop plant compatibility of the active compound combinations according to the invention is particularly pronounced in certain concentration ratios.
  • the weight ratios of the active ingredients in the drug combinations can be varied in relatively large ranges. In general, 1 part by weight of active compound of the formula (I)
  • Salts 0.001 to 1000 parts by weight, preferably 0.01 to 100 parts by weight, particularly preferably 0.05 to 20 parts by weight of one of the above under (b 1 ) said crop compatibility-improving compounds (antidotes / safeners).
  • the active compound combinations according to the invention are generally used in the form of ready-to-use formulations. However, the active ingredients contained in the active compound combinations can also be mixed in individual formulations during use, ie be applied in the form of tank mixes.
  • plant-compatible mineral or vegetable oils for example the commercial product "Rako Binol”
  • ammonium salts such as e.g. Ammonium sulfate or ammonium thiocyanate.
  • novel drug combinations can be used as such, in the form of their formulations or the use forms prepared therefrom by further dilution, such as ready-to-use solutions, suspensions, emulsions, powders, pastes and granules.
  • the application is done in customary, e.g. by pouring, spraying, spraying, dusts or spreading.
  • the application rates of the active compound combinations according to the invention can be varied within a certain range; they hang u.a. weather and soil factors. In general, the application rates are between 0.001 and 5 kg per ha, preferably between 0.005 and 2 kg per ha, more preferably between 0.01 and 0.5 kg per ha.
  • the active compound combinations according to the invention can be applied before and after the emergence of the plants, that is, in the pre-emergence and postemergence process.
  • the safeners to be used according to the invention can be used for pretreatment of the seed of the crop (seed dressing) or introduced into the seed furrows prior to sowing or applied separately before the herbicide or applied together with the herbicide before or after draining the plants become.
  • the important crops such as cereals (wheat, barley, rice), corn, soybean, potato, cotton, oilseed rape, beets, sugarcane and fruit plants (with the fruits apples, pears, citrus fruits and grapes) are mentioned, with cereals Corn, soybean, potato, cotton and oilseed rape are particularly noteworthy.
  • active ingredients always includes the active ingredient combinations mentioned here.
  • Toluolsulfonsöure is stirred for 8 h at room temperature. Thereafter, the reaction mixture is washed with 10% aqueous potassium carbonate solution, dried (magnesium sulfate) and concentrated by rotary evaporation.
  • WP wettable powders
  • test plants are laid out in sandy loam soil in wood fiber pots, covered with soil and grown in the greenhouse under good growth conditions. 2-3 weeks after sowing, the test plants are treated in the single leaf stage.
  • the test compounds formulated as wettable powders (WP) are sprayed onto the green plant parts in various dosages with a water application rate of 600 l / ha with the addition of 0.2% wetting agent.
  • WP wettable powders
  • the following compounds show an effect of> 80% in the preemergence with 320 g / ha ai against Alopecurus myosuroides, Echinocloa crus-gali Lolium multiflorum and Setaria viridis: Ia-18, Ia-20, 1-a-21, Ia-24, Ia-25, Ia-26, Ia-27, Ib-55, 1-B-56, 1-B-57, Ib-59, Ib-60, 1-b-73, I-b-76, Ib-77, Ib-78, Ib-79, 1-b-80, Ib-81, 1-b-82, 1-b-83, Ic-19, Ic-23, Ic-24, Ic-25, 1-c-26, Ie-17, Ie-18
  • Test plants are laid out in sandy loam in wood fiber pots or in plastic pots, covered with soil and grown in the greenhouse, during the growing season outdoors outside the greenhouse, under good growth conditions. 2-3 weeks after sowing, the test plants are treated in the one to three leaf stage.
  • the test compounds formulated as wettable powder (WP) or liquid (EC) are sprayed onto the plants and the soil surface in various dosages with a water application rate of 300 l / ha with the addition of wetting agent (0.2 to 0.3%).
  • WP wettable powder
  • EC liquid
  • Crop plants are sprayed before use of the test substances with the safener at a certain hectare application rate (usually 1 day before application of the test substances)
  • the safener is applied together with the test substance as a tank mix (indicating the amount of safener in g / ha or as a ratio to the herbicide).
  • the compounds according to the invention show, for example, a significantly better effect in the post-emergence process

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Abstract

L'invention concerne de nouveaux cyclopentane-1,3-diones substitués par 2,4,6-trialkylphényle de formule (I), dans laquelle X, Y, A, B, Q1, Q2 et G sont spécifiés ci-dessus. L'invention concerne également des procédés et des produits intermédiaires destinés à produire lesdits composés et leur utilisation en tant qu'agent pesticides et/ou herbicides ainsi que des agents herbicides sélectifs, qui contiennent d'une part les cyclopentane-1,3-diones substitués par 2,4,6-trialkylphényle de formule (I) et d'autre part au moins un composé améliorant la compatibilité avec des plantes de culture.
EP07702572A 2006-01-07 2007-01-03 Cyclopentane-1,3-dione substitue par 2,4,6-trialkylphenyle Withdrawn EP1976819A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102006000971A DE102006000971A1 (de) 2006-01-07 2006-01-07 2,4,6-Trialkylphenylsubstituierte Cyclopentan-1,3-dione
PCT/EP2007/000023 WO2007080066A2 (fr) 2006-01-07 2007-01-03 Cyclopentane-1,3-dione substitue par 2,4,6-trialkylphenyle

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EP1976819A2 true EP1976819A2 (fr) 2008-10-08

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US (1) US8168832B2 (fr)
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AU (1) AU2007204432A1 (fr)
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ZA200805807B (en) 2009-10-28
WO2007080066A3 (fr) 2007-11-08
CN101395116A (zh) 2009-03-25
JP2009522331A (ja) 2009-06-11
AR059134A1 (es) 2008-03-12
US20090137393A1 (en) 2009-05-28
DE102006000971A1 (de) 2007-07-12
US8168832B2 (en) 2012-05-01
WO2007080066A2 (fr) 2007-07-19
RU2008131800A (ru) 2010-02-20
CN101395116B (zh) 2013-04-17
BRPI0706419A2 (pt) 2011-03-29
UA93229C2 (ru) 2011-01-25
KR20080094676A (ko) 2008-10-23
CA2636352A1 (fr) 2007-07-19
AU2007204432A1 (en) 2007-07-19

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