EP2369927A2 - Association d'herbicide(s) et de phytoprotecteur(s) - Google Patents

Association d'herbicide(s) et de phytoprotecteur(s)

Info

Publication number
EP2369927A2
EP2369927A2 EP09756682A EP09756682A EP2369927A2 EP 2369927 A2 EP2369927 A2 EP 2369927A2 EP 09756682 A EP09756682 A EP 09756682A EP 09756682 A EP09756682 A EP 09756682A EP 2369927 A2 EP2369927 A2 EP 2369927A2
Authority
EP
European Patent Office
Prior art keywords
alkyl
hydrogen
compounds
haloalkyl
alkoxy
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Withdrawn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
EP09756682A
Other languages
German (de)
English (en)
Inventor
Christopher Hugh Rosinger
Erwin Hacker
Hartmut Ahrens
Hansjörg Dietrich
Frank Ziemer
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
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Priority to EP09756682A priority Critical patent/EP2369927A2/fr
Publication of EP2369927A2 publication Critical patent/EP2369927A2/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings

Definitions

  • the present invention relates to agrochemically active herbicide-safener combinations, to processes for their preparation and to their use for controlling harmful plants.
  • WO 2003/011853 are structurally different from those described in the compositions according to the invention, namely they have an aryl or heteroaryl substituent in the 6-position of pyridine.
  • WO 2007/082098 also discloses structurally different pyridine derivatives, namely also 6-aryl-substituted compounds.
  • WO 2006/062979 discloses the pyridine derivatives used in the composition according to the invention, the use of safeners in combination with these is only described generically. It is not described which safeners are suitable for the compounds, also no biological data are shown that demonstrate an actual safener effect.
  • the active ingredients in the compositions according to the invention are - if applied without safener - sometimes not fully compatible with some important crops such as various cereals, corn or rice. Therefore, they can not be used in some crops to ensure the desired broad herbicidal activity against harmful plants.
  • the object of the present invention is therefore to find herbicidal agents in which the selectivity of the abovementioned herbicides is increased in relation to important crop plants. This object is surprisingly achieved by the herbicide-safener combination according to the invention.
  • R 1 is hydrogen, fluorine or chlorine
  • R 2 is hydrogen, C 1 -C 4 alkyl optionally substituted with one to two R 7 , C 2 -C 4 alkenyl optionally substituted with one to two radicals
  • R 4 is halogen
  • R 5 is COOH or a herbicidally active derivative of COOH
  • R 6 is independently halogen, Ci-C 6 alkyl, Ci-C 6 haloalkyl, C 2 - Ce alkenyl, C 2 -C 6 haloalkenyl, C r C 3 alkoxy, dC 2 haloalkoxy, Ci- C 3 -
  • R 7 , R 8 and R 9 are each independently halogen, dC 3 -
  • R 10 independently of one another represent hydrogen, C 1 -C 4 -alkyl, C 1 -C 3 -haloalkyl,
  • R 11 is hydrogen, C 1 -C 4 alkyl, C 3 haloalkyl or CHR 24 C (O) OR 25 ;
  • R 12 is C 1 -C 4 alkyl or C 3 haloalkyl
  • R 14 is hydrogen or C 1 -C 4 alkyl
  • R 15 is hydrogen, C 1 -C 4 alkyl or phenyl optionally substituted with one to three R 27 radicals;
  • R 16 is hydrogen or C 1 -C 4 alkyl; or
  • R 15 and R 16 together represent - (CH 2 ) 4 - or - (CH 2 ) S -;
  • R 17 independently of one another are halogen, C 1 -C 3 -alkoxy, C 1 -C 3 -haloalkoxy,
  • R 18 independently represents halogen, Ci-C 3 alkyl, C- ⁇ -C 3 alkoxy, Ci- C3 haloalkoxy, Ci-C3 alkylthio, dC 3 haloalkylthio, amino, Ci-C 3 -
  • R 19 is hydrogen or C 1 -C 4 -alkyl
  • R 20 and R 21 independently of one another are hydrogen or C 1 -C 4 -alkyl; or
  • R 22 is hydrogen or C 1 -C 4 -alkyl
  • R 23 is C 1 -C 4 alkyl
  • R 24 is hydrogen, C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy
  • R 25 is hydrogen, C 1 -C 4 alkyl or benzyl
  • R 26 is hydrogen, C 1 -C 6 -alkyl, C 1 -C 3 -haloalkyl, C 1 -C 4 -alkoxy, phenyl, phenoxy or benzyloxy;
  • R 27 is independently methyl, chloro or methoxy;
  • O 1 represents 1, 2, 3, 4 or 5;
  • the herbicide-safener combinations according to the invention may contain additional other components, for example crop protection agents of another type and / or additives customary in plant protection and / or formulation auxiliaries, or be used together with them.
  • the herbicides (A) and safeners (B) can be applied in a known manner, for example jointly (for example as a co-formulation or as a tank mixture) or also as a splitting, e.g. on the plants, plant parts, plant seeds or the area on which the plants grow. It is possible, e.g. the application of the individual active substances or the herbicide-safener combination in several portions (sequence application), for. After pre-emergence applications, followed by post-emergence applications or early post-emergence applications, followed by mid-late applications
  • the abovementioned formula (I) comprises all stereoisomers and mixtures thereof, in particular also racemic mixtures, and - as far as enantiomers are possible - both enantiomers and in particular the respective biologically active enantiomer.
  • a herbicidally active derivative is salts, esters, carboxamides, acylhydrazides, imidates,
  • the salts of the compounds of the general formula (I) which are suitable in the field of crop protection are salts which are obtained by contacting with acids or bases or by ion exchange, so that the derived salts have sufficient water solubility for the bioavailability and thus the herbicidal activity.
  • the compounds of formula (I) can be further prepared by addition of a suitable inorganic or organic acid such as HCl, HBr, H 2 SO 4 , H 3 PO 4 , or HNO 3 , but also oxalic acid, acetic acid, butyric acid, fumaric acid, lactic acid, Malonic acid, propionic acid, salicylic acid, tartaric acid, pentanoic acids or sulfonic acids, such as para-toluenesulfonic acid, to form a basic group, such as amino or alkylamino salts.
  • a suitable inorganic or organic acid such as HCl, HBr, H 2 SO 4 , H 3 PO 4 , or HNO 3
  • oxalic acid acetic acid, butyric acid, fumaric acid, lactic acid, Malonic acid, propionic acid, salicylic acid, tartaric acid, pentanoic acids or sulfonic acids, such as para-toluenesul
  • Suitable substituents which are present in deprotonated form such as, for example, sulfonic acids or carboxylic acids, may be internal salts in turn protonatable groups, such as amino groups form. Salts can also be formed by replacing the hydrogen with a suitable cation for agriculture with suitable substituents, such as, for example, sulfonic acids or carboxylic acids.
  • salts are, for example, metal salts, in particular alkali metal salts or alkaline earth metal salts, in particular sodium and potassium salts, salts with organic amines, for example of dimethylamine, diethanolamine or triethanolamine, ammonium salts, in particular quaternary (quaternary) ammonium salts with cations of the formula [NRR'R "R '" ] + , wherein R to R 1 "each independently represent an organic radical, in particular alkyl, aryl, aralkyl or alkylaryl, or sulfonium salts, for example trimethylsulfonium salts.
  • ester and thioester derivatives of the carboxylic acid function of R 5 are also particularly suitable.
  • Ester groups result from the condensation of a carboxylic acid (CO 2 H) function with an alcohol (ie R AL OH) where R AL is a radical derived from the alcohol; a variety of methods are known for producing such esters.
  • Analogous thioester groups of the formula C (O) SR AL can be obtained as the condensation product of a carboxylic acid function with a thioalcohol (mercaptan) of the formula R AL SH; a variety of methods are also known to prepare such thioesters.
  • the corresponding ester or thioester compounds of the general formula (I) are easily hydrolyzed, for example by the presence of hydrolytically active enzymes, whereby the corresponding carboxylic acid function is again obtained.
  • the radical R AL has more than one OH or SH function
  • the radical may be condensed with more than one pyridine ring system of the general formula (I).
  • ester and thioester compounds of the general formula (I) are based in particular on ester or thioester formation with methanol, ethanol, butanol, 2-butoxyethanol, 2-ethylhexanol, isopropanol, 2-methylpropanol (isobutanol), octanol isomers (isoctanol) and Ethanethiol to give each methyl, ethyl, butyl, 2- Butoxyethyl, 2-ethylhexyl, isopropyl, 2-methylpropyl, isoctyl and Ethylthioester to form. Particularly preferred are the methyl and ethyl esters.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 29 is a divalent radical linking the carboxyl ester function CO 2 R 29 of each two pyridine ring systems of general formula (I), and the divalent radical is selected from the group consisting of -CH 2 -, - (CH 2 ) 2 -, - (CH 2 ) 3 - and -CH (CH 3 ) CH 2 -;
  • R 30 is hydrogen, C 1 -C 10 -alkyl, which may optionally be substituted by 1 to 3 radicals R 46 , or benzyl;
  • R 31 and R 32 are independently dC 4 alkyl or CrC 3 haloalkyl; or
  • R 31 and R 32 together are -CH 2 CH 2 -, -CH 2 CH (CH 3 ) - or - (CH 2 ) 3 -;
  • R 33 is hydrogen, Ci-C 4 alkyl, C 1 -C 4 -HaIOaIKyI or benzyl;
  • Alkoxycarbonyl or benzyl, - R 34 is hydrogen, dC 4 alkyl, C r C 4 haloalkyl, C 2 -C 4 alkylcarbonyl, C 2 -C 4;
  • R 35 is hydrogen, C r C 4 alkyl or dC 4 haloalkyl
  • R 36 is hydrogen, C r C 4 alkyl, hydroxy, C r C 4 alkoxy or S (O) 2 R 47 ;
  • R 37 is hydrogen or C 1 -C 4 alkyl
  • R 38, R 39 and R 40 is hydrogen or a radical which is selected from the group consisting of Ci-Cw-alkyl, C 3 -C 12 cycloalkyl, C 4 -C 12 alkylcycloalkyl, C 4 -C 12 -cycloalkylalkyl, C 2 -C 14 -alkenyl and C 2 -C 14 -alkynyl, where each radical may optionally be substituted by 1 to 3 radicals R 45 ;
  • Y is O, S or NR 48
  • R 41 is hydrogen, Ci-C 3 alkyl, -C 3 haloalkyl, C 2 -C 4 alkoxyalkyl, OH or C 1 -C 3 -alkoxy;
  • R 42 is C r C 3 alkyl, C 1 -C 12 haloalkyl or C 2 -C 4 alkoxyalkyl; or
  • R 41 and R 42 together form - (CH 2 J 2 -, -CH 2 CH (CH 3 ) - or - (CH 2 ) 3 -;
  • R 43 and R 44 are independently of each other C 1 -C 4 alkyl
  • each R 45 is independently selected from the group consisting of halogen, cyano, hydroxycarbonyl, C 2 -C 4 -alkoxycarbonyl, hydroxy, C 1 -C 4 -alkoxy, C 1 -C 4 -HaIOalkoxy, C 1 -C 4 - Alkylthio, C 1 -C 4 - Haloalkylthio, amino, C 1 -C 4 -alkylamino, C 2 -C 4 -dialkylamino, -CH [O (CH 2 ) n ] and phenyl which may optionally be substituted by 1 to 3 radicals R 49 ; or
  • R 45 together form -OC (O) O- or -O (C (R 50 ) (R 50 )) i -2 O-; or
  • R 45's are taken together as an oxygen atom to form a carbonyl with the carbon atom to which they are attached;
  • each R 46 is independently selected from the group consisting of halogen, Ci-C 4 alkoxy, -C 4 -haloalkoxy, C 1 -C 4 -AIKyKhJo, C 1 -C 4 - haloalkylthio, amino, Ci-C 4 - Alkylamino or C 2 -C 4 dialkylamino; or
  • R 46 are taken together as an oxygen atom to form a carbonyl radical with the carbon atom to which they are attached;
  • R 47 is C 1 -C 4 alkyl, C 1 -C 3 haloalkyl or NR 51 R 52 ;
  • R 48 is H, C r C 3 alkyl, C 1 -C 3 haloalkyl or C 2 -C 4 alkoxyalkyl;
  • each R 49 is independently selected from the group consisting of halogen, C 1 -C 4 -alkyl, C 1 -C 3 -HaIOaIKyI, hydroxy, C 1 -C 4 -alkoxy, C 1 - C 3 haloalkoxy, C -Al 1 -C 3 alkylthio, C 1 -C 3 -HaIOaIKyItIIiO, amino, C 1 -C 3 -
  • each R 50 is independently selected from the group consisting of hydrogen and C 1 -C 4 alkyl
  • R 51 and R 52 are independently selected from the group consisting of hydrogen or C 1 -C 4 alkyl; m is an integer of 2 to 3; and
  • n is an integer from 1 to 4.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 5 is CO 2 R 29 , CH 2 OR 30 or CHO.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 5 is CO 2 R 29 or CHO.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 5 is CO 2 R 29 .
  • the present invention encompasses compounds of the general formula (I) in which
  • R 29 is selected from the group consisting of hydrogen, C 1 -C 8 -AIRyI or d-alkyl which is substituted by phenyl, where the phenyl radical may optionally be substituted by 1 to 3 radicals R 45 .
  • the present invention encompasses compounds of the general formula (I) in which
  • R 29 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl or C 1 -C 4 -alkyl which is substituted by phenyl, where the phenyl radical optionally substituted with 1 to 3 radicals R 45 may be substituted.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 29 is selected from the group consisting of hydrogen, C 1 -C 4 alkyl or benzyl.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 36 is selected from the group consisting of hydrogen, C 1 -C 4 -alkyl, hydroxy or C 1 -C 4 -alkoxy.
  • the present invention relates to compounds of the general formula (I) in which
  • R 41 is selected from the group consisting of hydrogen, C 1 -C 3 alkyl, C 1 -C 3 haloalkyl or C 2 -C 4 alkoxyalkyl.
  • the present invention covers compounds of the general formula (I) in which
  • R 5 is selected from the group consisting of COOH, an agrochemically acceptable salt, an ester and a thioester derivative thereof.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 5 is selected from the group consisting of COOH, an agrochemically acceptable salt, and an ester derivative thereof.
  • the present invention relates to compounds of the general formula (I) in which
  • p is an integer from 0 to 2.
  • the present invention covers compounds of the general formula (I) in which
  • p is an integer from 0 to 1.
  • the present invention encompasses compounds of the general formula (I) in which
  • the present invention covers compounds of the general formula (I) in which
  • R 1 is hydrogen or F.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 1 is F or Cl.
  • the present invention covers compounds of the general formula (I) in which
  • R 1 is H.
  • the present invention encompasses compounds of the general formula (I) in which R 1 is F.
  • the present invention covers compounds of the general formula (I) in which
  • R 1 is Cl.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 2 is H, C (O) R 10 or C 1 -C 4 alkyl which may optionally be substituted with R 7 ;
  • the present invention encompasses compounds of the general formula (I) in which
  • R 2 is H, CH 3 or C (O) R 10 ;
  • R 3 is H or CH 3 ; or
  • the present invention covers compounds of the general formula (I) in which
  • R 2 is H, C (O) CH 3 or C 1 -C 4 alkyl which may optionally be substituted with R 7 ; and R 3 is H or C 1-4 alkyl.
  • the present invention encompasses compounds of the general formula (I) in which R 2 and R 3 are independently hydrogen or methyl.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 2 and R 3 are hydrogen.
  • the present invention includes compounds of the general formula (I) in which
  • R 4 is Br or Cl.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 4 is Cl.
  • the present invention encompasses compounds of the general formula (I) in which
  • each R 6 is independently halogen, C 1 -C 2 -alkyl or C 1 -C 2 -haloalkyl.
  • the present invention covers compounds of the general formula (I) in which
  • R 7 is halo, methoxy, fluoromethoxy, methylthio, fluoromethylthio, amino, methylamino, dimethylamino or methoxycarbonyl.
  • the present invention covers compounds of the general formula (I) in which R 10 is hydrogen or C 1 -C 3 alkyl.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 10 is hydrogen or CH 3 .
  • the present invention encompasses compounds of the general formula (I) in which
  • R 10 is CH 3 .
  • the present invention encompasses compounds of the general formula (I) in which
  • R 19 is hydrogen or C 1 -C 2 alkyl.
  • the present invention encompasses compounds of the general formula (I) in which
  • R 32 is hydrogen or CH 3 .
  • the present invention encompasses compounds of the general formula (I) in which
  • R 20 and R 21 are independently hydrogen or C 1 -C 2 alkyl.
  • the present invention covers compounds of the general formula (I) in which
  • R 20 and R 21 are independently hydrogen or CH 3 . Included in the compositions of the described embodiments are N-oxides and agrochemically acceptable salts thereof. Combinations of the embodiments 1 to 35 are shown by
  • R 29 represents a divalent radical linking the carboxyl ester function CO 2 R 29 of two pyridine ring systems of general formula (I), and the divalent radical is selected from the group consisting of -CH 2 -, - (CH 2 ) 2 -, - (CH 2 ) 3 - and -CH (CH 3 ) CH 2 -;
  • R 30 is hydrogen; Ci-Cio-alkyl, which optionally with 1 to 3
  • R 46 radicals may be substituted; or benzyl
  • R 31 and R 32 are independently C 1 -C 4 alkyl or C 1 -C 3 haloalkyl; or
  • R 31 and R 32 together represent -CH 2 CH 2 -, -CH 2 CH (CH 3 ) - or - (CH 2 J 3 -;
  • R 33 is hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or benzyl;
  • R 34 is hydrogen, dC 4 alkyl, Ci-C 4 haloalkyl, C 2 -C 4 alkylcarbonyl, C 2 -C 4 ⁇ lkoxycarbonyl or benzyl;
  • R 35 is hydrogen, C 1 -C 4 alkyl or C 1 -C 4 haloalkyl
  • R 36 is hydrogen, C r C 4 alkyl, hydroxy, C r C 4 alkoxy or S (O) 2 R 47 ;
  • R 37 is hydrogen or C 1 -C 4 alkyl
  • R 38 , R 39 and R 40 are hydrogen or a radical selected from the group consisting of C 1 -C 14 -
  • Y is O, S or NR 48 ;
  • R 41 is hydrogen, Ci-C 3 alkyl, -C 3 haloalkyl, C 2 -C 4 alkoxyalkyl, OH or C 1 -C 3 -alkoxy;
  • R 42 is C 1 -C 3 alkyl, C r C 3 haloalkyl or C 2 -C 4 alkoxyalkyl; or R 41 and R 42 together form - (CH 2 ) 2 -, -CH 2 CH (CH 3 ) - or - (CH 2 J 3 -, R 43 and R 44 independently of one another are C 1 -C 4 -alkyl each R 45 is independently selected from the group, consisting of halogen, cyano, hydroxycarbonyl, C 2 -C 4 - alkoxycarbonyl, hydroxy, -C 4 alkoxy, C 4 haloalkoxy, C 1 - C 4 alkylthio, -C 4 haloalkylthio, amino, Ci-C 4 - Alkylamino, C 2 -C 4 -dialkylamino, -CH [-O (CH 2 ) n -] and phenyl, which may be optionally substituted with 1 to 3 R 49 radicals;
  • two R 45 form an oxygen atom to form a carbonyl with the carbon atom to which they are attached;
  • each R 46 is independently selected from the group consisting of halogen, C 4 alkoxy, C 1 -C 4 -HaIOaIkOXy, C 1 - C 4 alkylthio, -C 4 haloalkylthio, amino, Ci-C 4 alkylamino and C 2 -C 4 dialkylamino; or
  • R 46 form an oxygen atom to form a carbonyl radical with the carbon atom to which they are attached;
  • R 4 4 7 ' is C 1 -C 4 -alkyl 1 -C 3 haloalkyl or NR 5 0 1 1; is;
  • R 3 4 4 8 0 is hydrogen, C 1 -C 3 -alkyl, C 1 -C 3 haloalkyl or C 2 -C 4 alkoxyalkyl;
  • each R 49 is independently selected from the group consisting of halogen, C 1 -C 4 -alkyl, C 1 -C 3 -haloalkyl, hydroxy,
  • each R 50 is independently selected from the group consisting of hydrogen and C 1 -C 4 alkyl;
  • R 51 and R 52 are independently hydrogen or C 1 -C 4 alkyl;
  • n is an integer of 2 to 3;
  • n is an integer from 1 to 4.
  • R 2 is hydrogen, CH 3 or C (O) R 10 ;
  • R 3 is hydrogen or CH 3 ;
  • R 2 and R 3 together form C (R 19 ) N (R 20 ) R 21 ;
  • R 10 , R 19 , R 20 and R 21 are each independently hydrogen or CH 3 ;
  • R 5 is CO 2 R 29 ;
  • R 2 and R 3 are hydrogen
  • R 29 is hydrogen, C 1 -C 4 alkyl or benzyl.
  • Specific embodiments include compounds of the general formula (I) selected from the group consisting of methyl 4-amino-3,5-dichloro-6-cyclopropyl-2-pyridinecarboxylate (Compound I-22 in Table A.1); 4-Amino-3,5-dichloro-6-cyclopropyl-2-pyridinecarboxylic acid (Compound 1-21 in Table A.1);
  • the compounds of the general formula (I) may also comprise N-oxides.
  • Corresponding pyridine-N-oxides are accessible via oxidation of the corresponding pyridines. Suitable oxidation methods are, for example, in Houben-Weyl, Methods of Organic Chemistry, Extension and follow-up volumes to the 4th edition, Volume E 7b, p 565 f. described.
  • radicals alkyl, alkoxyalkyl, hydroxyalkyl and alkoxyalkoxyalkyl can each be straight-chain or branched.
  • alkyl is understood to mean in particular the radicals methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, or the various isomers of pentyl or hexyl ,
  • alkoxyalkyl is understood to mean alkyl having an alkoxy substituent.
  • examples of the radical “alkoxyalkyl” include CH 3 OCH 2 , CH 3 OCH 2 CH 2 , CH 3 CH 2 OCH 2 , CH 3 CH 2 CH 2 CH 2 OCH 2 , CH 3 CH 2 OCH 2 CH 2 , CH 3 CH 2 CH 2 CH 2 OCH 2 CH 2 or CH 3 CH 2 CH 2 CH 2 OCH 2 CHMe.
  • alkoxyalkoxy is understood as meaning alkoxy provided with an alkoxy substituent.
  • alkoxyalkoxyalkyl is understood as meaning a radical in which an alkoxyalkoxy substituent is bonded to an alkyl radical.
  • alkoxyalkoxyalkyl include CH 3 OCH 2 OCH 2 , CH 3 OCH 2 OCH 2 CH 2 , CH 3 CH 2 OCH 3 OCH 2 and CH 3 OCH 3 CH 2 OCH 2 CH 2 .
  • hydroxyalkyl is understood to mean alkyl having a hydroxy substituent.
  • examples of “hydroxyalkyl” include HOCH 2 CH 2 , HOCH 2 CH 2 CH 2 and HOCH 2 CH 2 CH 2 CH 2 .
  • radicals with carbon atoms those having 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms, in particular 1 or 2 carbon atoms, are generally preferred.
  • the present invention also provides mixtures comprising stereoisomers which are encompassed by formula (I) or by the formulas of component B (safener).
  • Such compounds of the formula (I) or of the formulas of the component B (safener) contain, for example, one or more asymmetrically substituted carbon atoms or sulfoxides.
  • the possible stereoisomers defined by their specific spatial form, such as enantiomers and diastereomers, are all encompassed by the formula (I) or by the formulas of component B (safener) and can be obtained by conventional methods from mixtures of stereoisomers or also by stereoselective reactions in combination be prepared with the use of stereochemically pure starting or auxiliary materials.
  • the application rates are generally lower, z.
  • 0.1 g to 800 g a.i./ha preferably 1 g to 500 g a.i./ha, more preferably 10 g to 400 g a.i./ha.
  • the herbicides of the general formula (I) are suitable for controlling harmful plants, for example in plant nutritives, for example in economically important arable crops, for example monocotyledonous crops such as cereals (for example wheat, Barley, rye, oats), rice, maize, millet, or dicotyledonous crops such as sugarbeet, oilseed rape, cotton, sunflower and legumes, for example of the genera Glycine (eg Glycine max. (Soya) as non-transgenic Glycine max.
  • Glycine eg Glycine max. (Soya) as non-transgenic Glycine max.
  • Phaseolus Phaseolus, Pisum, Vicia and Arachis, or vegetable crops from various botanical groups such as potato, leek, cabbage, carrot, tomato, onion , as well as permanent and plantation crops such as pome and stone fruit, soft fruit, wine, Hevea, bananas, sugarcane, coffee, tea, citrus, nut orchards, turf, palm tree and forest crops.
  • botanical groups such as potato, leek, cabbage, carrot, tomato, onion , as well as permanent and plantation crops such as pome and stone fruit, soft fruit, wine, Hevea, bananas, sugarcane, coffee, tea, citrus, nut orchards, turf, palm tree and forest crops.
  • the herbicide-safener combinations (A) + (B) are also preferred, the use in cereals (eg wheat, barley, rye, oats), rice, corn, millet, sugar beet, sugar cane is particularly preferred , Sunflower, rapeseed and cotton.
  • the herbicide-safener combinations (A) + (B) are also useful in tolerant and non-tolerant mutant cultures and tolerant and intolerant transgenic cultures, preferably of corn, rice, corn, oilseed rape and soy, for example, those directed against imidazolinone herbicides. Atrazine, glufosinate or glyphosate are resistant.
  • the safeners contained as component (B) are understood to be compounds which are suitable for the phytotoxic effects of
  • Crop protection agents such as herbicides to reduce crops.
  • S1 a compounds from the group of heterocyclic carboxylic acid derivatives: S1 a ) compounds of the type of dichlorophenylpyrazoline-3-carboxylic acid (S1 a ), preferably compounds such as
  • S1 C derivatives of 1, 5-diphenylpyrazole-3-carboxylic acid (S1 C), preferably compounds such as ethyl 1- (2,4-dichlorophenyl) -5-phenylpyrazole-3-carboxylic acid ethyl ester (S1-5),
  • S1 d compounds of the type of the triazolecarboxylic acids (S1 d ), preferably
  • S1 e Compounds of the 5-benzyl- or carboxylic acid-5-phenyl-2-isoxazoline-3, or the 5,5-diphenyl-2-isoxazoline-3-carboxylic acid (S1 e), preferably compounds such as 5- ( 2,4-dichlorobenzyl) -2-isoxazoline-3-carboxylic acid ethyl ester (S1-8) or 5-phenyl-2-isoxazoline-3-carboxylic acid ethyl ester (S1-9) and related compounds as described in WO-A-91/08202 or 5,5-diphenyl-2-isoxazoline-carboxylic acid (S1-10) or 5,5-diphenyl-2- isoxazoline-carboxylic acid ethyl ester (S1-11) ("isoxadifen-ethyl") or n-propyl ester (S 1-12) or of 5- (4-fluorophenyl) -5
  • S2 a) Compounds of the 8-quinolinoxyacetic acid (S2 a), preferably (5-chloro-8-quinolinoxy) acetic acid, ethyl (1-methylhexyl) ester ( " Cloquintocetmexyl ") (S2-1), (5-chloro-8-quinolinoxy) acetic acid (1,3-dimethyl-but-1-yl) ester (S2-2), (5-chloro-8- quinolinoxy) acetic acid 4-allyl oxy-butyl ester (S2-3),
  • S2 b compounds of the (5-chloro-8-quinolinoxy) malonic acid type (S2 b ), preferably compounds such as (5-chloro-8-quinolinoxy) malonic acid diethyl ester, (5-chloro-8-quinolinoxy) malonic acid diallyl ester, ( 5-chloro-8-quinolinoxy) malonic acid methyl ethyl ester and related compounds as described in EP-A-0 582 198.
  • S3 Active substances of the dichloroacetamide type (S3), which are often used as pre-emergence safener (soil-active safener), such as. "Dichloromid” (N, N-diallyl-2,2-dichloroacetamide) (S3-1), "R-29148” (a-dichloroacetyl- ⁇ ⁇ . ⁇ -trimethyl-I .S-oxazolidine) from Stauffer
  • PPG-1292 N-allyl-N - [(1,3-dioxolan-2-yl) -methyl] -dichloroacetamide
  • AD-67 or "MON 4660” (3-dichloroacetyl-1-oxa-3-aza-spiro [4,5] decane) of
  • TI-35 (1-dichloroacetyl-azepane) from TRI-Chemical RT (S3-8),
  • Diaclonone (dicyclonone) (synonym: “BAS145138” or “LAB145138”) (RS) -I-dichloroacetyl-3,3,8a-trimethyl-perhydropyrrolo [1,2-a] -pyhmidin-6-one from the company
  • R A 1 is (Ci-C 6 ) alkyl, (C 3 -C 6 ) cycloalkyl, where the 2 latter radicals by v A substituents selected from the group consisting of halogen, (Ci-C 4 ) alkoxy, (Ci-C 6 ) Halo - Alkoxy and (Ci-C 4 ) alkylthio and in the case of cyclic radicals by (Ci-C 4 ) alkyl and (Ci-C 4 ) haloalkyl are substituted;
  • R A 2 is halogen, (dC 4) alkyl, (C 1 -C 4) -alkoxy, CF 3; m A 1 or 2; v A is 0, 1, 2 or 3;
  • RB 1 , RB 2 independently of one another hydrogen, (C 1 -C 6 ) AIKyI,
  • RB 1 cyclopropyl
  • RB 1 cyclopropyl
  • Rc 1, Rc 2 are independently hydrogen, (Ci-C ⁇ ) alkyl, (C 3 -C 8) cycloalkyl, (C 3 -C 6) alkenyl, (C 3 -C 6) alkynyl,
  • Rc 3 is halogen, (C 1 -C 4 ) alkyl, (C 1 -C 4 ) Al koxy, CF 3 mc is 1 or 2;
  • Active ingredients from the class of hydroxyaromatics and aromatic-aliphatic carboxylic acid derivatives e.g. 3,4,5-triacetoxybenzoic acid ethyl ester, 3,5-dimethoxy-4-hydroxybenzoic acid, 3,5-dihydroxybenzoic acid, 4-hydroxysalicylic acid, 4-fluorosalicyclic acid, 2-hydroxycinnamic acid, 2,4-dichlorocinnamic acid, as described in US Pat WO-A-2004/084631, WO-A-2005/015994, WO-A-2005/016001.
  • S5 Active ingredients from the class of hydroxyaromatics and aromatic-aliphatic carboxylic acid derivatives (S5), e.g. 3,4,5-triacetoxybenzoic acid ethyl ester, 3,5-dimethoxy-4-hydroxybenzoic acid, 3,5-dihydroxybenzoic acid, 4-hydroxysalicylic acid, 4-fluorosalicyclic acid, 2-hydroxycinnamic acid
  • S6 active compounds from the class of 1, 2-dihydroquinoxaline-2-ones (S6), e.g.
  • R D 1 is halogen, (C 1 -C 4) -alkyl, (Ci-C 4) haloalkyl, (C 1 -C 4) -alkoxy, (C 1 -C 4) HaIOaIkOXy,
  • R D 2 is hydrogen or (C 1 -C 4 ) alkyl
  • R D 3 is hydrogen, (C r C 8 ) alkyl, (C 2 -C 4 ) alkenyl, (C 2 -C 4 ) alkynyl, or aryl, where each of the aforementioned C-containing radicals is unsubstituted or substituted by one or more preferably up to three identical or different radicals from the
  • a group consisting of halogen and alkoxy is substituted; or their salts no is an integer from 0 to 2.
  • RE 2 (C 1 -C 16 ) alkyl, (C 2 -C 6 ) alkenyl, (C 3 -C 6 ) cycloalkyl, aryl; Benzyl, halobenzyl, RE 3 is hydrogen or (C 1 -C 6 ) AlkYl.
  • S11) oxyimino compound type compounds (S11) known as seed dressings such as those described in US Pat. B.
  • Oxabetrinil ((Z) -1,3-dioxolan-2-ylmethoxyimino (phenyl) acetonitrile) (S11-1), which is known as a seedling safener for millet against damage from metolachlor,
  • Fluorofenim (1- (4-chlorophenyl) -2,2,2-trifluoro-1-ethanone O- (1,3-dioxolan-2-ylmethyl) -oxime) (S1 1-2), which was used as seed dressing -Safener for millet is known against damage from metolachlor, and
  • Cyometrinil or “CGA-43089” ((Z) -cyanomethoxyimino (phenyl) acetonitrile) (S1 1-3), which is known as a seed dressing safener for millet against damage by metolachlor.
  • S12 Isothiochromanone (S12) class agents, e.g. Methyl - [(3-oxo-1H-2-benzothiopyran-4 (3H) -ylidene) methoxy] acetate (CAS No. 205121-04-6) (S12-1) and related compounds of WO-A -1998 / 13361.
  • S12 Isothiochromanone (S12) class agents, e.g. Methyl - [(3-oxo-1H-2-benzothiopyran-4 (3H) -ylidene) methoxy] acetate (CAS No. 205121-04-6) (S12-1) and related compounds of WO-A -1998 / 13361.
  • Seed pickling safener for maize known for damage from thiocarbamate herbicides
  • Pretilachlor is known in seeded rice, "flurazole” (benzyl-2-chloro-4-trifluoromethyl-1, 3-thiazole-5-carboxylate) (S13-3), which is used as a seed dressing safener for millet against damage by alachlor and
  • S 14 active substances which, in addition to a herbicidal activity against harmful plants, also have safener action on crops such as rice, such as, for example, rice.
  • crops such as rice, such as, for example, rice.
  • "Dimepiperate” or "MY-93" S-1-methyl-1-phenylethyl-piperidine-1-carbothioate) known as safener for rice against damages of the herbicide Molinate
  • NK 049 3,3'-dimethyl-4-methoxy-benzophenone
  • COD (1-bromo-4- (chloromethylsulfonyl) benzene) by Kumiai, (CAS No. 54091-06-4), which is known as a safener against damage of some herbicides in rice.
  • component (A) is a compound of formula (I) selected from methyl 4-amino-3,5-dichloro-6-cyclopropyl-2-pyridinecarboxylate, 4-amino-3,5-dichloro-6-cyclopropyl 2-pyridinecarboxylic acid, methyl 4-amino-3-chloro-6-cyclopropyl-2-pyridinecarboxylate, 4-amino-3-chloro-6-cyclopropyl-2-pyridinecarboxylic acid, methyl-4-amino-3-chloro-6-yl cyclopropyl-5-fluoro-2-pyridinecarboxylate and 4-amino-3-chloro-6-cyclopropyl- ⁇ -fluoro-pyridinecarboxylic acid and as component (B) a safener selected from mefenpyr-diethyl (S1-1), isoxadifen- ethyl (S1-11), cy
  • herbicide-safener combinations comprising (A) a herbicidally effective amount of one or more compounds of the formula (I) or salts thereof, and (B) an antidote-effective amount of one or more safeners.
  • herbicidally effective amount means an amount of one or more herbicides which is suitable for negatively influencing plant growth.
  • Antidote effective amount in the sense of the invention means an amount of one or more safeners which is suitable for reducing the phytotoxic effect of crop protection active ingredients (for example of herbicides) on crop plants.
  • the safeners (B) are suitable for reducing the phytotoxic effects that can occur when using herbicides of the general formula (I) in crops without significantly impairing the effectiveness of these herbicidal active compounds against harmful plants.
  • the field of application of conventional crop protection agents can be considerably extended, e.g. on crops in which the use of herbicides was previously not possible or only possible to a limited extent.
  • the required application rates of the safeners can vary within wide limits depending on the indication and the herbicidal active ingredient used and are in usually in the range of 0.001 to 5 kg, preferably 0.005 to 2.5 kg of active ingredient per hectare.
  • the herbicidal active compounds (A) of the general formula (I) and the safeners (B) may be applied together (for example as a ready-to-use formulation or in the tank-mix process) or in any desired order, e.g. by spraying, pouring and spraying or by granule scattering.
  • the weight ratio herbicide of the general formula (I) (A): safener (B) can vary within wide limits and is preferably in the range from 1: 10,000 to 10,000: 1, in particular from 1: 1000 to 1000: 1.
  • safener (B) depend on the type of herbicide used and the safener used, as well as on the species and stage of development of the crop to be treated, and can be determined on a case-by-case basis by simple, routine preliminary tests.
  • (B) may, depending on their properties, be used to pre-treat the seed of the crop (e.g., seed dressing) or seeded into the seed furrows prior to sowing, or applied together with the herbicide before or after emergence of the plants.
  • Pre-emergence treatment includes both the treatment of the area under cultivation (including possibly on the acreage, for example in rice applications) before sowing and the treatment of the sown, but not overgrown cultivated areas.
  • the seed eg grains, seeds or vegetative propagules such as tubers or sprouts with buds
  • seedlings with the safeners (B) optionally in combination with other agrochemical active ingredients pretreated.
  • the active ingredients can be brought to the seed, for example by pickling, or the active ingredients and the seed can be added to water or other solvents, and the active substances are absorbed, for example, by addition or diffusion in the dipping process or by swelling or pre-germination.
  • the young plants can be brought into contact, for example by spraying, dipping or pouring, with the safeners, optionally in combination with other agrochemical active substances, and subsequently transplanted and optionally treated with the herbicides (A).
  • Seedling or seedling treatment may be carried out with the safeners (B) alone or in conjunction with other agrochemical active substances - such as fungicides, insecticides or plant-strengthening agents, fertilizers or to speed up the swelling and germination processes.
  • the safeners after the pretreatment application can then be applied again before, after or together with one or more herbicides of the formula (I), possibly also in combination with other known herbicides. By pre-treating the seed or seedlings, an improved long-term effect of the safeners can be achieved.
  • the present invention thus further provides a method for controlling unwanted plants in plant crops, which is characterized in that the components (A) and (B) of the inventive
  • Herbicide-safener combination on the plants eg harmful plants such as monocotyledonous or dicotyledonous weeds or unwanted crops
  • the seed eg grains, seeds or vegetative propagules such as tubers or sprouts with buds
  • the area on which the plants grow eg the acreage
  • one or more safeners (B) preferably one or more, in particular one, compound of groups (S1) to (S14) before, after or simultaneously with the herbicide (s) of general formula (I) (A) on the plants, the seed or the area on which the plants grow (eg the acreage) are applied.
  • the safeners (B) are used for seed treatment.
  • Undesirable plants are understood to mean all plants that grow in places where they are undesirable. These may be, for example, harmful plants (for example monocotyledonous or dicotyledonous weeds or undesired crop plants), for example those which are resistant to certain herbicidal active substances such as glyphosate, atrazine, glufosinate or imidazolinone herbicides.
  • harmful plants for example monocotyledonous or dicotyledonous weeds or undesired crop plants
  • herbicidal active substances such as glyphosate, atrazine, glufosinate or imidazolinone herbicides.
  • Monocotyledonous weeds are derived e.g. the genera Echinochloa, Setaria, Panicum, Digitaria, Phleum, Poa, Festuca, Eleusine, Brachiaria, Lolium, Bromus, Avena, Cyperus, Sorghum, Agropyron, Cynodon, Monochoria, Fimbristylis, Sagittaria, Eleocharis, Scirpus, Paspalum, Ishaemum, Sphenoclea, Dactyloctenium, Agrostis, Alopecurus, Apera. Dicotyledonous weeds are derived e.g.
  • an effective amount of components (A) and (B) for controlling harmful plants in crops for example in economically important arable crops, for example monocotyledonous crops such as cereals (eg wheat, barley, rye, oats), rice, maize , Millet, or dicotyledonous crops such as sugarbeet, oilseed rape, cotton, sunflowers and legumes, for example of the genera Glycine (eg Glycine max., Such as non-transgenic glycine max. (Eg conventional strains such as STS strains) or transgenic glycine max.
  • Glycine eg Glycine max.
  • non-transgenic glycine max. Eg conventional strains such as STS strains
  • transgenic glycine max transgenic glycine max.
  • Soy or LL soy) and their crosses Phaseolus, Pisum, Vicia and Arachis, or vegetable crops from various botanical groups such as potato, leek, cabbage, carrot, tomato, onion, as well as long-term and plantation crops such as pome and stone fruit, berry fruit , Wine, hevea, bananas, sugar cane, coffee, tea, citrus, nut orchards, turf, palm tree and forest crops.
  • the invention also relates to the use of the herbicide-safener combinations according to the invention for controlling undesired plant growth, preferably in plant crops.
  • the herbicide-safener combinations of the invention may be prepared by known methods, e.g. be prepared as mixed formulations of the individual components, optionally with other active ingredients, additives and / or customary formulation auxiliaries, which are then diluted with water used in the usual way, or as so-called tank mixes by common dilution of the separately formulated or partially formulated separately
  • the herbicide-safener combination according to the invention can also be used for controlling harmful plants in crops of known or yet to be developed genetically modified plants.
  • the transgenic plants are usually characterized by particular advantageous properties, for example by resistance to certain pesticides, especially certain herbicides, resistance to plant diseases or pathogens of plant diseases such as certain insects or microorganisms such as fungi, bacteria or viruses.
  • Other special properties relate to z. B. the crop in terms of quantity, quality,
  • transgenic plants with increased starch content or altered quality of starch or those known with other fatty acid composition of the crop may be in a tolerance or resistance to abiotic stressors z. As heat, cold, drought, salt and ultraviolet radiation.
  • the application of the herbicide-safener combinations according to the invention or their salts in economically important transgenic crops of useful and ornamental plants eg.
  • cereals such as wheat, barley, rye, oats, millet, rice, cassava and corn or cultures of sugar beet, cotton, soy, rape, potato, tomato, pea and other vegetables.
  • Crop plants are used, which are resistant to the phytotoxic effects of herbicides or have been made genetically resistant.
  • Glufosinate see, for example, EP-A-0242236, EP-A-242246) or glyphosate (WO
  • Transgenic crop plants with modified fatty acid composition (WO 91/13972). genetically modified crops with new content or secondary substances z.
  • Transgenic crop plants which produce pharmaceutically or diagnostically important proteins (molecular pharming") - transgenic crops which are characterized by higher yields or better quality transgenic crop plants which are characterized by a combination of, for example, the above-mentioned new properties (“gene stacking").
  • nucleic acid molecules can be introduced into plasmids that allow mutagenesis or sequence alteration by recombination of DNA sequences. With the help of standard methods z. For example, base substitutions are made, partial sequences are removed, or natural or synthetic sequences are added.
  • adapters or linkers can be attached to the fragments, see, for example, US Pat. Sambrook et al., 1989, Molecular Cloning, A Laboratory Manual, 2nd ed. CoId Spring Harbor Laboratory Press, ColD Spring Harbor, NY; or Winnacker "Genes and Clones", VCH Weinheim 2nd edition 1996
  • the production of plant cells having a reduced activity of a gene product can be achieved, for example, by the expression at least a corresponding antisense RNA, a sense RNA to obtain a cosuppression effect or the expression of at least one appropriately engineered ribozyme which specifically cleaves transcripts of the above gene product.
  • DNA molecules may be used which comprise the entire coding sequence of a gene product, including any flanking sequences that may be present, as well as DNA molecules which comprise only parts of the coding sequence, which parts must be long enough to be present in the cells to cause an antisense effect. It is also possible to use DNA sequences which have a high degree of homology to the coding sequences of a gene product but are not completely identical.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

L'invention concerne une composition contenant (A) un ou plusieurs composés de formule (I), leurs N-oxydes ou leurs sels, les symboles et indices individuels étant tels que définis dans la description, et (B) un ou plusieurs phytoprotecteurs.
EP09756682A 2008-11-29 2009-11-21 Association d'herbicide(s) et de phytoprotecteur(s) Withdrawn EP2369927A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP09756682A EP2369927A2 (fr) 2008-11-29 2009-11-21 Association d'herbicide(s) et de phytoprotecteur(s)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP08020781A EP2210492A1 (fr) 2008-11-29 2008-11-29 Combinaison d'herbicide-phytoprotecteur
EP09756682A EP2369927A2 (fr) 2008-11-29 2009-11-21 Association d'herbicide(s) et de phytoprotecteur(s)
PCT/EP2009/008302 WO2010060579A2 (fr) 2008-11-29 2009-11-21 Association d'herbicide(s) et de phytoprotecteur(s)

Publications (1)

Publication Number Publication Date
EP2369927A2 true EP2369927A2 (fr) 2011-10-05

Family

ID=40793079

Family Applications (2)

Application Number Title Priority Date Filing Date
EP08020781A Withdrawn EP2210492A1 (fr) 2008-11-29 2008-11-29 Combinaison d'herbicide-phytoprotecteur
EP09756682A Withdrawn EP2369927A2 (fr) 2008-11-29 2009-11-21 Association d'herbicide(s) et de phytoprotecteur(s)

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP08020781A Withdrawn EP2210492A1 (fr) 2008-11-29 2008-11-29 Combinaison d'herbicide-phytoprotecteur

Country Status (7)

Country Link
US (1) US20100137136A1 (fr)
EP (2) EP2210492A1 (fr)
JP (1) JP2012510435A (fr)
CN (1) CN102223795A (fr)
AR (1) AR075482A1 (fr)
BR (1) BRPI0922081A2 (fr)
WO (1) WO2010060579A2 (fr)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2486717A (en) * 2010-12-22 2012-06-27 Syngenta Ltd Substituted 4-aminopicolinate herbicides with safeners
CA2903643C (fr) * 2013-03-05 2022-05-24 Bayer Cropscience Ag Utilisation de derives de quinoleine pour ameliorer le rendement agricole
CN103814895B (zh) * 2014-03-20 2016-03-30 黑龙江省农业科学院植物保护研究所 一种减低除草剂残留药害的拌种剂及其制备方法
AR101858A1 (es) * 2014-09-15 2017-01-18 Dow Agrosciences Llc Composiciones herbicidas protegidas que comprenden un herbicida de ácido piridincarboxílico
TWI685302B (zh) * 2014-09-15 2020-02-21 美商陶氏農業科學公司 包含吡啶羧酸除草劑之安全的除草組成物
JP7680764B2 (ja) * 2019-09-27 2025-05-21 ザ ボード オブ トラスティーズ オブ ザ ユニバーシティ オブ アーカンソー グループ１５除草剤に対するイネの保護
PH12022552733A1 (en) 2020-04-21 2024-03-18 Kumiai Chemical Industry Co Methane-production inhibitor composition and method for inhibiting methane production

Family Cites Families (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA19709A1 (fr) 1982-02-17 1983-10-01 Ciba Geigy Ag Application de derives de quinoleine a la protection des plantes cultivees .
ATE103902T1 (de) 1982-05-07 1994-04-15 Ciba Geigy Ag Verwendung von chinolinderivaten zum schuetzen von kulturpflanzen.
EP0131624B1 (fr) 1983-01-17 1992-09-16 Monsanto Company Plasmides de transformation de cellules vegetales
BR8404834A (pt) 1983-09-26 1985-08-13 Agrigenetics Res Ass Metodo para modificar geneticamente uma celula vegetal
JPS6087254A (ja) 1983-10-19 1985-05-16 Japan Carlit Co Ltd:The 新規尿素化合物及びそれを含有する除草剤
DE3525205A1 (de) 1984-09-11 1986-03-20 Hoechst Ag, 6230 Frankfurt Pflanzenschuetzende mittel auf basis von 1,2,4-triazolderivaten sowie neue derivate des 1,2,4-triazols
BR8600161A (pt) 1985-01-18 1986-09-23 Plant Genetic Systems Nv Gene quimerico,vetores de plasmidio hibrido,intermediario,processo para controlar insetos em agricultura ou horticultura,composicao inseticida,processo para transformar celulas de plantas para expressar uma toxina de polipeptideo produzida por bacillus thuringiensis,planta,semente de planta,cultura de celulas e plasmidio
DE3680212D1 (de) 1985-02-14 1991-08-22 Ciba Geigy Ag Verwendung von chinolinderivaten zum schuetzen von kulturpflanzen.
ATE80182T1 (de) 1985-10-25 1992-09-15 Monsanto Co Pflanzenvektoren.
ATE57390T1 (de) 1986-03-11 1990-10-15 Plant Genetic Systems Nv Durch gentechnologie erhaltene und gegen glutaminsynthetase-inhibitoren resistente pflanzenzellen.
IL83348A (en) 1986-08-26 1995-12-08 Du Pont Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
US5013659A (en) 1987-07-27 1991-05-07 E. I. Du Pont De Nemours And Company Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase
DE3633840A1 (de) 1986-10-04 1988-04-14 Hoechst Ag Phenylpyrazolcarbonsaeurederivate, ihre herstellung und verwendung als pflanzenwachstumsregulatoren und safener
DE3775527D1 (de) 1986-10-22 1992-02-06 Ciba Geigy Ag 1,5-diphenylpyrazol-3-carbonsaeurederivate zum schuetzen von kulturpflanzen.
DE3733017A1 (de) 1987-09-30 1989-04-13 Bayer Ag Stilbensynthase-gen
DE3808896A1 (de) 1988-03-17 1989-09-28 Hoechst Ag Pflanzenschuetzende mittel auf basis von pyrazolcarbonsaeurederivaten
DE3817192A1 (de) 1988-05-20 1989-11-30 Hoechst Ag 1,2,4-triazolderivate enthaltende pflanzenschuetzende mittel sowie neue derivate des 1,2,4-triazols
EP0365484B1 (fr) 1988-10-20 1993-01-07 Ciba-Geigy Ag Sulfamoylphénylurées
DE3939010A1 (de) 1989-11-25 1991-05-29 Hoechst Ag Isoxazoline, verfahren zu ihrer herstellung und ihre verwendung als pflanzenschuetzende mittel
DE3939503A1 (de) 1989-11-30 1991-06-06 Hoechst Ag Neue pyrazoline zum schutz von kulturpflanzen gegenueber herbiziden
ATE241007T1 (de) 1990-03-16 2003-06-15 Calgene Llc Dnas, die für pflanzliche desaturasen kodieren und deren anwendungen
EP0536293B1 (fr) 1990-06-18 2002-01-30 Monsanto Technology LLC Plantes a teneur en amidon augmentee
CA2083948C (fr) 1990-06-25 2001-05-15 Ganesh M. Kishore Plantes tolerantes au glyphosate
DE4107396A1 (de) 1990-06-29 1992-01-02 Bayer Ag Stilbensynthase-gene aus weinrebe
SE467358B (sv) 1990-12-21 1992-07-06 Amylogene Hb Genteknisk foeraendring av potatis foer bildning av staerkelse av amylopektintyp
EP0492366B1 (fr) 1990-12-21 1997-03-26 Hoechst Schering AgrEvo GmbH Nouveaux dérivés de chloro-5-quinoline-8-acide oxyalkanecarboniques, procédé pour leur préparation et leur utilisation comme antidote d'herbicides
DE4104782B4 (de) 1991-02-13 2006-05-11 Bayer Cropscience Gmbh Neue Plasmide, enthaltend DNA-Sequenzen, die Veränderungen der Karbohydratkonzentration und Karbohydratzusammensetzung in Pflanzen hervorrufen, sowie Pflanzen und Pflanzenzellen enthaltend dieses Plasmide
TW259690B (fr) 1992-08-01 1995-10-11 Hoechst Ag
DE4331448A1 (de) 1993-09-16 1995-03-23 Hoechst Schering Agrevo Gmbh Substituierte Isoxazoline, Verfahren zu deren Herstellung, diese enthaltende Mittel und deren Verwendung als Safener
DE19621522A1 (de) 1996-05-29 1997-12-04 Hoechst Schering Agrevo Gmbh Neue N-Acylsulfonamide, neue Mischungen aus Herbiziden und Antidots und deren Verwendung
US6294504B1 (en) 1996-09-26 2001-09-25 Syngenta Crop Protection, Inc. Herbicidal composition
DE19652961A1 (de) 1996-12-19 1998-06-25 Hoechst Schering Agrevo Gmbh Neue 2-Fluoracrylsäurederivate, neue Mischungen aus Herbiziden und Antidots und deren Verwendung
US6071856A (en) 1997-03-04 2000-06-06 Zeneca Limited Herbicidal compositions for acetochlor in rice
DE19727410A1 (de) 1997-06-27 1999-01-07 Hoechst Schering Agrevo Gmbh 3-(5-Tetrazolylcarbonyl)-2-chinolone und diese enthaltende nutzpflanzenschützende Mittel
DE19742951A1 (de) * 1997-09-29 1999-04-15 Hoechst Schering Agrevo Gmbh Acylsulfamoylbenzoesäureamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung
WO2001035740A2 (fr) * 1999-11-17 2001-05-25 Bayer Aktiengesellschaft Herbicides selectifs a base de derives de pyridine 2,6-disubstituee
AR031027A1 (es) 2000-10-23 2003-09-03 Syngenta Participations Ag Composiciones agroquimicas
US6635306B2 (en) * 2001-06-22 2003-10-21 University Of Cincinnati Light emissive display with a black or color dielectric layer
AR037228A1 (es) 2001-07-30 2004-11-03 Dow Agrosciences Llc Compuestos del acido 6-(aril o heteroaril)-4-aminopicolinico, composicion herbicida que los comprende y metodo para controlar vegetacion no deseada
CN1764374B (zh) 2003-03-26 2010-09-22 拜尔作物科学股份公司 芳族羟基化合物用作安全剂的用途
DE10335726A1 (de) 2003-08-05 2005-03-03 Bayer Cropscience Gmbh Verwendung von Hydroxyaromaten als Safener
DE10335725A1 (de) 2003-08-05 2005-03-03 Bayer Cropscience Gmbh Safener auf Basis aromatisch-aliphatischer Carbonsäuredarivate
DE102004023332A1 (de) 2004-05-12 2006-01-19 Bayer Cropscience Gmbh Chinoxalin-2-on-derivate, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung und deren Verwendung
WO2006062979A1 (fr) 2004-12-06 2006-06-15 E.I. Dupont De Nemours And Company Derives herbicides d'acide 4-aminopicolinique 6-cyclopropyl-substitues
WO2007023719A1 (fr) 2005-08-22 2007-03-01 Kumiai Chemical Industry Co., Ltd. Agent servant à réduire l'attaque chimique et composition herbicide produisant une attaque chimique réduite
WO2007023764A1 (fr) 2005-08-26 2007-03-01 Kumiai Chemical Industry Co., Ltd. Agent servant à réduire les effets nocifs d’un herbicide et composition d’herbicide ayant des effets nocifs réduits
MY143535A (en) * 2006-01-13 2011-05-31 Dow Agrosciences Llc 6-(poly-substituted aryl)-4-aminopicolinates and their use as herbicides

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2010060579A3 *

Also Published As

Publication number Publication date
WO2010060579A2 (fr) 2010-06-03
WO2010060579A3 (fr) 2010-07-29
AR075482A1 (es) 2011-04-06
CN102223795A (zh) 2011-10-19
EP2210492A1 (fr) 2010-07-28
US20100137136A1 (en) 2010-06-03
BRPI0922081A2 (pt) 2015-08-11
JP2012510435A (ja) 2012-05-10

Similar Documents

Publication Publication Date Title
EP3638665B1 (fr) Herbicides efficaces a base de 3-phenylisoxazoline-5-carboxamides d'acides et d'esters carboxyliques de tetrahydro et dihydrofurane
EP3668845B1 (fr) Herbicides efficaces de 3-phénylisoxazolin-5-carboxamide des acides et des esters carboniques cyclopentyles
EP2369929A2 (fr) Association d'herbicide(s) et de phytoprotecteur(s)
EP2369922A2 (fr) Combinaison herbicide-phytoprotecteur
EP2773208A1 (fr) Compositions d'herbicides et de phytoprotecteurs contenant des n-(tétrazol-5-yl)- et n-(triazol-5-yl)arylcarboxamides
EP2369927A2 (fr) Association d'herbicide(s) et de phytoprotecteur(s)
EP3599857B1 (fr) Mélanges herbicides
EP3793977A1 (fr) Pyrrolin-2-ones à substitution 2-bromo-6-alcoxyphényle et leur utilisation comme herbicides
EP4232443B1 (fr) Dérivés de 1-(pyridyl)-5-azinylpyrazole et leur utilisation pour lutter contre la croissance végétale indésirable
EP3938348A1 (fr) Nouvelles 3-(2-brome-4-alkinyl-6-alkoxyphényl)-3-pyrroline-2-ones et leur utilisation comme herbicides
EP3823450A1 (fr) Mélanges herbicides contenant de l'aclonifène et du cinméthyline
WO2019219584A1 (fr) Nouvelles spirocyclohexylpyrrolin-2-ones et leur utilisation comme herbicides
EP2369931A2 (fr) Association d'herbicides et de phytoprotecteurs
WO2019228788A1 (fr) Pyrorroline-2-ones à substitution 2-bromo-6-alcoxyphényle et leur utilisation comme herbicides
EP3618620A1 (fr) Compositions de phytoprotection contenant des dérivés de quinazolindion-6-carbonyle
WO2019228787A1 (fr) 2-alkyle-6-alcoxyphényle-pyrroline-2-ones à substitution spéciale et leur utilisation comme herbicides
WO2019166305A1 (fr) Benzamides bicycliques à action herbicide
WO2011138280A2 (fr) Combinaison herbicides-phytoprotecteurs contenant des arylpyridazinones et des phytoprotecteurs
WO2021209486A1 (fr) Pyrroline-2-ones à substitution spécifique et leur utilisation en tant qu'herbicides
EP3938346A1 (fr) 3-(2-halogène-6-alkyl-4-propinylphényl)-3-pyrroline-2-ones à substitution spéciale et leur utilisation comme herbicides
EP3938349A1 (fr) 3-(2-alkoxy-6-alkyl-4-propinylphényl)-3-pyrroline-2-ones à substitution spéciale et leur utilisation comme herbicides
WO2019219588A1 (fr) Nouvelles 2-alkyl-6-alcoxyphényl-3-pyrroliin-2-ones à substitution spéciale et leur utilisation comme herbicides
EP3938347A1 (fr) 3-phényl-5-spirocyclopentyl-3-pyrrolin-2-ones à substitution spécifique et leur utilisation en tant qu'herbicides
EP3360417A1 (fr) Utilisation de sulfonylindole en tant que herbicide
EA042560B1 (ru) Гербицидные смеси

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20110629

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20130603

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20131214