Abstract:
Pyridine derivatives have the formula (I), in which the index and substituents have the following meanings: X is cyano, nitro, halogen, alkyl, alkyl halide, alkoxy, alkoxy halide and cycloalkyl; n equals 0, 1, 2 or 3; Y is oxygen or nitrogen; R is C(CO2CH3)=CHCH3, C(CO2CH3)=CHOCH3, C(CO2CH3)=NOCH3, C(CONH2)=NOCH3 or C(CONHCH3)=NOCH3; and R and R have the meanings given in the description. Also disclosed are their salts, a process for preparing the same and their use for controlling animal pests and harmful fungi.
Abstract translation:式(I),其中,所述索引和所述取代基具有以下含义的吡啶衍生物:X是氰基,硝基,卤素,烷基,卤代烷基,烷氧基,卤代烷氧基和环烷基; n为0,1,2或3; Y是氧或氮; R C(CO 2 CH 3)= CHCH 3,C(CO 2 CH 3)= CHOCH 3,C(CO 2 CH 3)= NOCH 3,C(CONH 2)= NOCH 3或C(CONHCH 3)= NOCH 3; 和R <1>和R <2>具有说明书中给出的含义; 和它们的盐,它们的制备方法以及它们用于控制动物害虫和有害真菌中的用途。
Abstract:
This invention concerns a fungicide mixture containing, in synergistically effective quantities, a) a carbamate of formula (I), in which T stands for CH or N, n for 0, 1 or 2, and R stands for halogen, C1C4-alkyl or C1C4-alkyl halide, where the radicals R can be different if n stands for 2, and/or b) an oxime ether of formula (II), in which the substitents have the following meaning: X is oxygen or amino (NH), Y is CH or N; Z is oxygen, sulphur, amino (NH) or C1C4-alkyl amino (N-C1-C4-alkyl); R' is C1C6-alkyl, C1C6-alkyl halide, C3C6-alkenyl, C2C6-alkenyl halide, C3C6-alkinyl, C3C6-alkinyl halide, C3C6-cycloalkyl-methyl or benzyl, which can be either partially or completely halognized and/or can carry one to three of the following radicals: cyano, C1C4-alkyl, C1C4-alkyl halide, C1C4-alkoxy, C1C4-alkoxy halide, and C1C4-alkylthio, and c) an acaricide from the group of compounds (III.a) to (III.d).
Abstract:
This invention concerns fungicide mixtures containing in a synergistically effective amount a) an oxime ether of the formula (I), in which the substituents have the following meaning: X is oxygen or amino (NH), Y is CH or N; Z is oxygen, sulphur, amino (NH) or C1-C4-alkyl amino (N-C1-C4-alkyl); R' is C1-C6-alkyl, C1-C6-alkyl halide, C3-C6-alkenyl, C2-C6-alkenyl halide, C3-C6-alkinyl, C3-C6-alkinyl halide, C3-C6-cycloalkyl-methyl or benzyl, which can be either partially or completely halogenated and/or can carry one to three of the following radicals: cyano, C1-C4-alkyl, C1-C4-alkyl halide, C1-C4-alkoxy, C1-C4-alkoxy halide, and C1-C4-alkylthio, and/or b) a carbamate of the formula (II), in which T stands for CH or N, n is 0, 1 or 2, and R stands for halogen, C1-C4-alkyl, C1-C4-alkyl halide, where the radicals R can be different if n is 2, and c(+/-)-(2-chlorophenyl)4-chlorophenyl)(pyrimidin-5-yl)-methanol (III).
Abstract:
The invention concerns pyrimidine derivatives of formula (I) in which the substituents have the following meanings: X is C(CO2CH3)=NOCH3, C(CONHCH3)=NOCH3, C(CO2CH3)=CHOCH3, C(CO2CH3)=CHCH3, N(CO2CH3)-OCH3; R and R , independently of each other, are hydrogen, C1-C4 alkyl, C1-C4 alkyl halide or C1-C4 alkoxy; A is (i), the bond designated * being bonded to Y; R is hydrogen, C1-C4 alkyl, C1-C4 alkyl halide, phenoxy C1-C4 alkyl, C3-C6 cycloalkyl, cyano, C1-C4 alkoxy, hydroxy, halogen; R is hydrogen, C1-C8 alkyl, C1-C4 alkyl halide, C1-C6 cyanoalkyl, C1-C4 alkoxy-C1-C4 alkyl, C2-C4 alkenyloxy-C1-C4 alkyl, C1-C4 alkoxy halide-C1-C4 alkyl, C1-C4 oxoalkyl, C2-C4 alkenyl, C2-C4 alkinyl, C2-C4 alkenyl halide, C2-C4 alkinyl halide, C3-C6 cycloalkyl, C3-C6 cycloalkyl-C1-C4 alkyl, C1-C4 alkoxy; Y is hydrogen, hydroxy, halogen, optionally substituted aryl, hetaryl, cycloalkyl, cycloalkenyl, heterocyclyl, alkyl, alkenyl, alkinyl, alkyl halide, alkoxy, aryloxy, arylthio, hetaryloxy, hetarylthio, alkylthio or cycloalkyloxy; A not meaning -O- when X stands for C(CO2CH3)=CHOCH3. The invention also concerns the salts of these derivatives, a process and intermediate products for their preparation, and pesticides and fungicides containing them.
Abstract:
The invention relates to cyanimino oxime ethers of formula (I), in which X is NOCH3, CHOCH3, CHCH3; Y is O, NZ, where Z is H, alkyl; R is H, alkyl; R is cyano, nitro, trifluoromethyl, halogen, alkyl, alcoxy; m is 0, 1, 2, the radicals R possibly being different when m is 2; R is H, cyano, alkyl, alkylhalide, alkoxy or cycloalkyl; R is H, optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, heterocyclyl. The invention also relates to salts of said ethers, and the process and intermediates for the preparation and use thereof for the control of noxious fungi and animal pests.
Abstract:
2-(O-[pyrimidin-4-yl]methylenoxy)phenyl acetic acid derivatives are disclosed having the general formula (I), as well as their salts and N-oxides. In the formula, the radicals R to R and Q have the following meanings: R stands for hydrogen or alkyl; R stands for halogen, alkyl or alkyl halide; R stands for hydrogen, amino, hydroxy, mercapto, halogen, optionally phenyl-substituted alkyl, alkyl halide, alkoxyalkyl, alkoxy, monoalkylamino, dialkylamino, alkylthio, alkylsulphoxyl, alkylsulphonyl, cycloalkyl, trialkylsilyloxy or in the aromatic ring optionally substituted phenyl, phenoxy, phenoxymethyl, benzyloxy or heteroaryl; R stands for hydrogen, cyano, halogen, alkyl, alkyl halide or alkoxy; Q stands for C(=NOCH3)-CONHCH3, C(=NOCH3)-COOCH3 or N(OCH3)-COOCH3. Also disclosed are their salts and N-oxides and their use for controlling harmful fungi and animal pests.
Abstract:
The invention relates to pyridyl carbamates of formula (I), in which the index and the substituents have the follwing meaning: R' is hydrogen, optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, alkyl carbonyl and alkoxy carbonyl; R" is optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, or where V is an amino group, also hydrogen; V is oxygen (-O-), sulphur (-S-) or an amino group which can carry one of the following radicals: alkyl, alkenyl, alkinyl or cycloalkyl; X is cyano, nitro, halogen, optionally substituted alkyl, alkenyl, alkinyl, alkoxy, alkenyloxy, alkinyloxy, or where n > 1, an optionally substituted bridge bound to two adjacent C-atoms of the pyridyl ring and containing 3 to 4 members from the group of 3 or 4 carbon atoms, 2 to 3 carbon atoms and one or two nitrogen, oxygen and/or sulphur atoms, said bridge being able to form a partially unsaturated or aromatic radical together with the ring to which it is bound; n is 0, 1, 2 or 3, and the radicals X may be different when n > 1; R is halogen, hydroxy, mercapto, amino, formyl, carboxyl, carbonylamino or an organic radical which is bound directly or via an oxy group, mercapto group, amino group, carboxyl or carbonylamino group, or along with one group X and the pyridyl ring to which they are bound, an optionally substituted bicyclic, partially or completely unsaturated system which can contain heteroatoms from the group of oxygen, sulphur and nitrogen in addition to carbon ring members. It also relates to a process and intermediates for the preparation of said pyridil carbamates and use thereof.
Abstract:
The invention relates to phenylacetic acid derivatives of the formula (I), in which the substituents and the index have the following meaning: X is NOCH3, CHOCH3, CHCH3 and CHCH2CH3; Y is NR and O; R , R are hydrogen and alkyl; R is cyano, nitro, halogen, alkyl, alkyl halide and alkoxy; m is 0, 1 or 2; R is hydrogen, hydroxy, amino, cyano, halogen, alkyl, alkyl halide, cycloalkyl, alkoxy, alkylthio, alkylamino and dialkylamino; A is a 5 or 6 membered hetero-aromatic ring; R is a substituted aryl; R is hydrogen, optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, heterocyclyl, aryl and hetaryl. The invention also relates to the salts of said derivatives, a process and intermediates for the preparation and use thereof.
Abstract:
The invention concerns pyridylacetic acid derivatives of formula (I), in which the substituents and the index have the following meanings: X - NOCH3, CHOCH3, CHCH3 and CHCH2CH3; Y - oxygen or NR', R' representing hydrogen or alkyl; R - cyano, nitro, trifluoromethyl, halogen, alkyl and alkoxy; m is 0, 1 or 2; R is hydrogen and alkyl; R - hydrogen, cyano, nitro, hydroxy, amino, halogen, alkyl, alkyl halide, alkoxy, alkoxy halide, alkyl thio, alkylamino or dialkylamino; R - hydrogen, cyano, nitro, hydroxy, amino, halogen; or optionally substituted alkyl, alkoxy, alkylthio, alkylamino, dialkylamino, alkenyl, alkenyloxy, alkenylthio, alkenylamino, N-alkenyl-N-alkylamino, alkinyl, alkinyloxy, alkinylthio, alkinylamino, N-alkinyl-N-alkylamino, cycloalkyl, cycloalkyloxy, cycloalkylthio, cycloalkylamino, N-cycloalkyl-N-alkylamino, cycloalkenyl, cycloalkenyloxy, cycloalkenylthio, cycloalkenylamino, N-cycloalkenyl-N-alkylamino, heterocyclyl, heterocyclyloxy, heterocyclylthio, heterocyclylamino, N-heterocyclyl-N-alkylamino,aryl, aryloxy, arylthio,arylamino, N-aryl-N-alkylamino, hetaryl, hetaryloxy, hetarylthio, hetarylamino, and N-hetaryl-N-alkylamino; R - hydrogen, optionally substituted alkyl, alkenyl, alkinyl, alkylcarbonyl, alkenylcarbonyl, alkinylcarbonyl, alkylsulphonyl, cycloalkyl, aryl, arylcarbonyl, arylsulphonyl, hetaryl, hetarylcarbonyl, or hetarylsulphonyl. Also disclosed are the salts of the above derivatives,and methods and intermediate products for producing them and agents containing them.
Abstract:
The invention concerns a fungicidal mixture containing: a) an oxime ether carboxylic acid amide of formula (I) in which R stands for hydrogen or halogen; and either b.1) the oxime ether carboxylic acid ester of formula (IIa); b.2) the oxime ether carboxylic acid amide of formula (IIb); or b.3) the methoxyacrylic acid ester of formula (IIc), in a synergistically active amount.