Abstract:
The invention relates to cyclohexenondioxothiochromanoyl derivatives of formula (I) wherein the variables have the following meanings: X is oxygen, sulphur, S=O, S(=O)2, CR R , C=O or C=NR ; R is hydrogen, nitro, halogen, cyano, alkyl, alkyl halide, alkoxy, halogenalkoxy, alkylthio, halogenalkylthio, alkylsulfinyl, halogenalkylsulfinyl, alkylsulfonyl, halogenalkylsulfonyl, optionally substituted aminosulfonyl or optionally substituted sulfonylamino; R is alkyl, alkyl halide, alkoxy or halogenalkoxy; R is hydrogen, alkyl or halogen; and R , R are hydrogen, nitro, halogen, cyano, alkyl, alkyl halide, alkoxy, halogenalkoxy, alkylthio, halogenalkylthio, alkylsulfinyl, halogenalkylsulfinyl, alkylsulfonyl, halogenalkylsulfonyl or substituted amino; or R and R together form a chain which can be substituted and/or interrupted by oxygen or sulphur; or an optionally substituted methylide group; l is 0 to 4; R is substituted (3-oxo-1-cyclohexen-2-yl)-carbonyl or substituted (1,3-dioxo-2-cyclohexyl-methylides. The invention also relates to the agriculturally usable salts of said derivatives, to methods for producing the derivatives, to substances containing them, and to the use of the derivatives or substances containing them for combating undesirable plants.
Abstract:
The invention relates to tricyclic cyclohexanedione derivatives of formula (I) in which the substituents have the following meaning: R is hydrogen, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 haloalkylthio, C1-C6 alkylsulfinyl, C1-C6 haloalkylsulfinyl, C1-C6 alkylsulfonyl, C1-C6 haloalkylsulfonyl, halogen, cyano or nitro; X is O or NR ; R is hydrogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, C1-C6 haloalkoxy, phenyl that is optionally substituted with C1-C3 alkyl, halogen, cyano, nitro or C1-C3 alkylsulfonyl or phenylsulfonyl that is optionally substituted with C1-C3 alkyl, halogen, cyano or nitro; R , R is hydrogen, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 haloalkylthio, C1-C6 alkylsulfinyl, C1-C6 haloalkylsulfinyl, C1-C6 alkylsulfonyl, C1-C6 haloalkylsulfonyl, NR R , C2-C6 alkoxyalkyl, C1-C6 alkoxycarbonyl, C1-C6 alkylcarbonyl, halogen, cyano, nitro, phenyl that is optionally substituted with C1-C3 alkyl, halogen, cyano or nitro; R is hydrogen or C1-C4 alkyl; R is hydrogen, C1-C6 alkyl or halogen; R is hydrogen or C1-C6 alkyl; R is C1-C6 alkyl or C1-C6 alkoxy; 1 is 0, 1 or 2; n is 1 or 2; R is substituted (3-oxo-1-cyclohexene-2-yl)carbonyl or substituted (1,3-dioxo-2-cyclohexyl)methylidene. The invention also relates to the agriculturally useful salts of the compounds (I), to methods for producing said tricyclic cyclohexanedione derivatives and to the intermediates for their production. The invention encompasses agents containing the inventive compounds and the use of said derivatives or of agents containing them for weed control.
Abstract:
The present invention relates to benzoyl-substituted alanines of the formula I in which the variables A and R 1 to R 12 have the meanings stated in the description, and to their agriculturally usable salts, methods and intermediates for their preparation, and the use of these compounds or compositions comprising these compounds for controlling unwanted plants.
Abstract:
A synergistic herbicidal mixture comprising A) at least one 3-heterocyclyl-substituted benzoyl derivative of the formula (I) in which the variables have the following meanings: R , R are halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; R is a optionally substituted heterocyclic radical se-lected from the group: isoxazol-3-yl, isoxazol-4-yl, isoxazol-5-yl, 4,5-dihydroisoxazol-3-yl, 4,5-dihydro-isoxazol-4-yl and 4,5-dihydroisoxazol-5-yl; R is hydrogen, halogen or alkyl; R is alkyl; R is hydrogen or alkyl; or one of its environmentally compatible salts; and B) the compound of formula (II) or one of its environmentally compatible salts; and C) at least one further herbicidal compound from the group of the acetolactate synthase inhibitors (ALS), lipid biosynthesis inhibitors and photosynthesis inhibitors; in a synergistically effective amount. Compositions comprising these mixtures, processes for the prepa-ration of these compositions, and their use for controlling undesired plants.
Abstract translation:一种协同除草混合物,其包含A)至少一种式(I)的3-杂环基取代的苯甲酰基衍生物,其中所述变量具有以下含义:R 1,R 3为卤素,烷基,卤代烷基,烷氧基, 卤代烷氧基,烷硫基,烷基亚磺酰基或烷基磺酰基; R 2是选自以下的任选取代的杂环基:异恶唑-3-基,异恶唑-4-基,异恶唑-5-基,4,5-二氢异恶唑-3-基,4,5-二氢 - 异恶唑-4-基和4,5-二氢异恶唑-5-基; R 4是氢,卤素或烷基; R 5是烷基; R 6是氢或烷基; 或其环境相容的盐之一; 和B)式(II)化合物或其与环境相容的盐之一; 和C)来自乙酰乳酸合酶抑制剂(ALS),脂质生物合成抑制剂和光合作用抑制剂的至少一种另外的除草化合物; 协同有效量。 包含这些混合物的组合物,这些组合物的制备方法以及它们用于防治不期望的植物的用途。
Abstract:
The invention relates to 4-haloalkyltriazine compounds of general formula (I), where R , R , R , R , A, X, and Ar have the meanings given in claim 1 and use of said compounds as herbicides.
Abstract:
The invention relates to tricyclic benzoylcyclohexanedione derivatives of formula (I), wherein the variables have the following meanings: X is oxygen, sulphur, S=O, S(=O)2, CR R , NR or a bond; y forms a saturated, partially saturated or unsaturated 5- or 6-membered heterocycle with the two carbons to which it is bonded; R , R , R , R is hydrogen, alkyl, alkyl halide, alkoxy or alkoxy halide; R is halogen, alkyl, alkyl halide, alkoxy or alkoxy halide; R is hydrogen, nitro, halogen, cyano, alkyl, alkyl halide, alkoxy, alkoxy halide, alkylthio, C1-C6- alkylthio halide, alkylsulfinyl, alkylsulfinyl halide, alkylsulfonyl, alkylsulfonyl halide, optionally substituted aminosulfonyl, or optionally substituted sulfonylamino; R is hydrogen, alkyl or halogen; m is 0, 1 or 2; R is hydrogen, alkyl, alkyl halide, alkylcarbonyl, formyl, alkoxycarbonyl, alkoxycarbonyl halide, alkylsulfonyl or alkylsulfonyl halide; and R is substituted (3-oxo-1-cyclohexen-2-yl)-carbonyl or substituted (1,3-dioxo-2-cyclohexyl)-methylidene; and to agriculturally useable salts thereof. The invention also relates to a method for producing the tricyclic benzoylcyclohexanedione derivatives, to products containing them and to the use of said derivatives or said products containing them for combating unwanted vegetation.
Abstract:
The invention relates to 3-(heterocyclyl)-substituted benzoylpyrazols of formula (I), wherein the variables have the following meanings: X is O, NH or N-alkyl; R is alkyl; R , R , R , R are hydrogen, alkyl or alkyl halide; R is halogen, nitro, alkyl halide, alkoxy, halogenalkoxy, alkylthio, halogenalkylthio, alkylsulfonyl or halogenalkylsulfonyl; R is hydroxy, alkoxy, alkenyloxy, alkylsulfonyloxy, alkylcarbonyloxy, alkylthiocarbonyloxy, phenylsulfonyloxy or phenylcarbonyloxy, and the phenyl radical can be substituted; R , R are alkyl; R is hydrogen or alkyl; and R is hydrogen or alkyl; and to their agriculturally useable salts. The invention also relates to intermediate products and methods for producing the inventive compounds and to the use of these compounds or products containing them for combating undesirable plants.
Abstract translation:本发明涉及式(I)的3-(杂环基) - 取代的苯甲酰基吡唑,其中各变量具有以下含义:X为O,NH或N-烷基; R 1烷基; R 2,R 3,R 4,R 5,氢,烷基或卤代烷基; R 6是卤素,硝基,卤代烷基,烷氧基,卤代烷氧基,烷硫基,卤代烷硫基,烷基磺酰基或卤代烷基磺酰基; R 7是羟基,烷氧基,烯氧基,烷基磺酰氧基,烷基羰基氧基,烷基硫代羰基氧基,苯基磺酰氧基或苯基羰基氧基,其中苯基可以被取代; R 8,R 9烷基; R 10是氢或烷基; R 11是氢或烷基; 及其农业上有用的盐。 中间体及其制备过程; 以及这些化合物或含有它们的药剂用于防治有害植物的用途。
Abstract:
The invention relates to benzylidene pyrazolones of formula (I), wherein the substituents and index n have the following meanings: R = optionally substituted C1-C6 alkyl; R = optionally substituted C1-C6 alkyl, optionally substituted C1-C6 alkoxy, halogen, nitro, cyano; R = hydrogen, halogen, nitro, cyano, a group NR R , OCOR , NR COR ,CO2R , -COSR , -CONR R , C1-C4-alkoxyiminoalkyl, C1-C6 alkoxycarbonyl, optionally substituted C1-C6 alkyl, optionally substituted C1-C6 alkoxy, optionally substituted C1-C6 alkylthio, optionally substituted C2-C6 alkenyl, optionally substituted phenyl, optionally substituted phenoxy, an optionally substituted 5- or 6-membered saturated or unsaturated heterocycle which can contain up to 4 nitrogen atoms and/or up to 2 oxygen or sulphur atoms as ring members; R = C1-C6 alkyl, C1-C4 halogen alkyl; or R and R = an optionally substituted saturated or unsaturated 2- or 3-membered bridge which can contain one sulphur atom which can be oxidized into sulfoxide or sulfone, R = hydrogen or optionally substituted C1-C6 alkyl; R = hydrogen, C1-C6 alkyl or C1-C4 halogenalkyl; n = 0, 1 or 2; X = hydrogen, chlorine or bromine. The compounds to which claim is laid are available in both a trans and a cis form or can be a mixture of these isomers.
Abstract:
The invention relates to a method for producing anellated tetrahydro-[1H]-triazoles of formula I wherein the variables R , Z, Z , X, W, n and Q have the designations cited in patent claim 1, by cyclising compounds of general formula II wherein R represents C(X)OR or C(X)SR , X represents oxygen or sulphur, and R has the designation cited in patent claim 1, in the presence of a base. The invention also relates to compounds of general formula I wherein W represents sulphur if Z represents a methylene group which is optionally substituted by R , as well as other compounds of formula I wherein Q represents a benzoxazole or benzothiazole radical. The invention further relates to the uses of said compounds as herbicides.
Abstract:
The invention relates to pyrazolyl derivatives of bicyclic benzoic acids of the general formula (I), wherein X, R and R are defined as indicated in claim 1. The invention also relates to herbicidal agents that contain the pyrazolyl derivatives of formula (I), to a method of producing said agents and to a method of combating undesired plant growth using the pyrazolyl derivatives of formula (I).