http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-109203-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e0bf0928b608797b70bbc2b91c7e52e |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P13-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-54 |
| filingDate | 2017-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2018-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-109203-A1 |
| titleOfInvention | METHOD TO CONTROL PPO RESISTANT WEEDS |
| abstract | Claim 1: A method for controlling the growth of weeds resistant to PPO, characterized in that it comprises contacting such weeds, parts thereof, their propagation material or their habitat, with compounds of the formula (1), wherein R¹ is H , F or Cl; R² is F, Cl, Br, CN, C (O) NH₂ or C (S) NH; R³ is H, F, Cl, CH₃ or OCH₃; R⁴ is H, CN, CH₃, CF₃, OCH₃, OC₂H₅, SCH₃, SC₂H₅, (CO) OC₂H₅ or CH₂R⁶, where R⁶ is F, Cl, OCH₃, SCH₃, SC₂H₅, CH₂F, CH₂Br or CH₂OH; R⁵ is (C₁₋₆-alkyl) amino, (C₁₋₆-dialkyl) amino, (NH) OR⁷, OH, OR⁸ or SR⁸, wherein R⁷ is CH₃, C₂H₅ or phenyl; and R⁸ are C₁₋₆-alkyl, C₂₋₆-alkenyl, C₃₋₆-alkynyl, C₁₋₆-haloalkyl, C₁₋₆-alkoxy-C₁₋₆-alkyl, C₁₋₆-alkoxy-C₁₋₆-alkoxy -C₁₋₆-alkyl, C₂₋₆-cyanoalkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl, C₁₋₄-alkyl-carbonyl-amino, C₁₋₆-alkylsulfinyl-C₁₋₆-alkyl, C₁ ₋₆-alkylsulfonyl-C₁₋₆-alkyl, C₁₋₆-dialkoxy-C₁₋₆-alkyl, C₁₋₆-alkylcarbonyloxy-C₁₋₆-alkyl, phenyl-carbonyl-C₁₋₆-alkyl, tri (C₁ ₋₃-alkyl) -silyl-C₁₋₆-alkyl, tri (C₁₋₃-alkyl) -silyl-C₂₋₆-alkenyl, tri (C₁₋₃-alkyl) -silyl-C₂₋₆-alkynyl, tri ( C₁₋₃-alkyl) -silyl-C₁₋₆-alkoxy-C₁₋₆-alkyl, dimethylamino, tetrahydropyranyl, tetrahydrofuranyl-C₁₋₃-alkyl, phenyl-C₁₋₆-alkoxy-C₁₋₆-alkyl, phenyl -C₁₋₃-alkyl, pyridyl-C₁₋₃-alkyl, pyridyl or phenyl, wherein the pyridyl and phenyl rings are independently substituted each other, with 1 to 5 substituents selected from the group consisting of halogen, C₁₋₃-alkyl or C₁₋₂-haloalkyl; C₃₋₆-cycloalkyl or C₃₋₆-cycloalkyl-C₁₋₄-alkyl, wherein the cycloalkyl rings are, independently from each other, unsubstituted or substituted with 1 to 5 substituents selected from the group consisting of halogen, C₁₋₃ -alkyl and C₁₋₂-haloalkyl; X is O, S, S (O) or S (O) ₂; Y is N or CH; and Z is O, S, S (O) or S (O) ₂; wherein the PPO resistant weeds are weed resistant to PPO inhibitor herbicides, except the compounds of the formula (1). Claim 9: The method according to any one of claims 1 to 8, characterized in that the compound of the formula (1) is selected from the compounds of the formulas (2) and (3). Claim 10: The method according to any one of claims 1 to 9, characterized in that a herbicidal composition comprising at least one compound of the formula (1) and at least one additional compound selected from herbicides B and / or protectors C is applied Claim 11: The method according to claim 10, characterized in that herbicide B is selected from herbicides of classes b1) to b15): b1) lipid biosynthesis inhibitors; b2) acetolactate synthase inhibitors (ALS inhibitors); b3) photosynthesis inhibitors; b4) protoporphyrinogen-IX oxidase inhibitors (PPO inhibitors) different from the compounds of the formula (1); b5) bleaching herbicides; b6) enolpiruvil shiquimate 3-phosphate synthase inhibitors (EPSP inhibitors); b7) glutamine synthetase inhibitors; b8) 7,8-dihydropteroate synthase inhibitors (DHP inhibitors); b9) mitosis inhibitors; b10) inhibitors of the synthesis of very long chain fatty acids (VLCFA inhibitors); b11) cellulose biosynthesis inhibitors; b12) decoupling herbicides; b13) auxinic herbicides; b14) auxin transport inhibitors; and b15) other herbicides selected from the group consisting of bromobutide, chlorflurenol, chlorflurenol-methyl, cinmethylin, cumyluron, dalapon, dazomet, diphezoquat, diphezoquat-methyl sulfate, dimethipin, DSMA, dymron, endothal and their salts, etobenzanid, flamproprop- flamproprop isopropyl, flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl, flurenol, flurenol-butyl, flurprimidol, fosamine, fosamine-ammonium, indanofan, indaziflam, maleic hydrazide, mefluidide, metam, methiozolin- (CAS 403640-7 7), methyl azide, methyl bromide, methyl-dymron, methyl iodide, MSMA, oleic acid, oxaziclomefone, pelargonic acid, pyributicarb, quinoclamine, triaziflam, tridiphane and 6-chloro-3- (2-cyclopropyl-6- methylphenoxy) -4-pyridazinol (CAS 499223-49-3), and their salts and esters; which includes its acceptable salts or derivatives in agriculture. Claim 12: The method according to any one of claims 1 to 11, characterized in that an agrochemical composition comprising at least one compound of the formula (1) and usual auxiliaries for formulating crop protection agents, and optionally, is applied to the less an additional compound selected from herbicides B and / or protectors C. Claim 13: The use of compounds of the formula (1), as defined in claims 1 or 9, to control weeds resistant to PPO. Claim 14: The use of the composition, as defined in claims 10 or 11, for controlling weeds resistant to PPO. |
| priorityDate | 2016-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 184.