Abstract:
The invention relates to 3-(4,5-dihydroisoxazol-3-yl)-substituted benzoylpyrazole of formula (I), wherein R represents C1-C4-halogenalkyl and R to R and R to R have the meanings given in the description. The inventive compounds have a herbidical effect.
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).
Abstract:
The invention relates to thiochromanoyl cyclohexenone derivatives of formula (I), wherein the variables have the following meanings: A is an optionally substituted, saturated or unsaturated alkyl chain; R is cyano, rhodano, nitro, OR , SR , SOR , SO2R , ONR NR , ON=CR R , NR R , P(O)R R , P(S)R R , CO2R , optionally substituted phenyl or heterocyclyl; R is alkyl, alkyl halide, alkoxy or halogenalkoxy; R is hydrogen, alkyl or halogen; X is oxygen, sulphur, S=O, S(=O)2, CR R , C=O or C=NR ; m is 0, 1 or 2; n is 0, 1, 2, 3 or 4; R is substituted (3-oxo-1-cyclohexen-2-yl)-carbonyl or substituted (1,3-dioxo-2-cyclohexyl)-methylidene; and to their agriculturally useful salts. The invention relates to intermediate products and methods for producing thiochromanoyl cyclohexenone derivatives, to products containing them and the use of these derivatives or products containing them for combating unwanted plants.
Abstract:
The invention relates to a method for producing compounds of formula (I), whereby: a) a bicyclic olefin of formula (II) is reacted with haloform in the presence of a base to produce the ring-enlarged product of formula (III); b) the compound of formula (III) is hydrolyzed to produce the allyl alcohol of formula (IV); c) the allyl alcohol of formula (IV) is oxidized to produce the unsaturated ketone of formula (V); d) the ketone of formula (V) is reacted with a nucleophilic ion Y, which stabilizes a negative charge, to produce the ketone of formula (VI), and; e) the ketone of formula (VI) is hydrolyzed to produce the bicyclic 1,3-diketone of formula (I). In formulas (I) to (VI), R -R , X, Y and Z have the meanings as cited in the description. The invention also relates to novel intermediate products and to novel methods for producing these intermediate products.
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 present invention relates to a crystalline form of 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1-(2H)-pyrimidinyl]-4-fluoro-N-[[methyl-(1-methylethyl)amino]sulphonyl]benzamide. The invention also relates to a method for preparing this crystalline form and to formulations for crop protection which comprise this crystalline form of the phenyluracil.
Abstract:
The invention relates to cyclopropyl-anellated 3-(4,5-dihydroisoxazol-3-yl)-substituted benzoylpyrazoles of formula (I), wherein the variables have the meanings given in the description, and to the agriculturally usable salts. Said compounds have a herbicidal effect.
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.