Abstract:
The invention relates to thiazolimines derivatives of formula (I), wherein the substituents have the following meanings: X, Y independently of each other stand for hydrogen, halogen, C1-C4-alkyl, C1-C4-haloalkyl, Z means hydrogen, C1-C8-alkyl, C2-C8-alkenyl, C2-C8-alkinyl, C1-C8-alkoxy, C1-C8-alkylthio, wherein these groups can be substituted by 1-5 halogen or C1-C4-alkoxy; aryl, hetaryl, benzyl, wherein these groups can be substituted with C1-C4-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy, halogen, nitro or cyano; or one of the following groups (a...); R1, R2 are hydrogen, halogen; C¿1?-C4-alkyl, C2-C4-alkenyl, C2-C4-alkinyl, wherein these groups can be substituted by 1-5 halogen or by C1-C4-alkoxy; n is 1 or 2; m is 0, 1 or 2, and R?3-R6¿ have the meaning cited in the application. The invention further relates to salts of compound I which can be used in agriculture.
Abstract:
The invention relates to a method for producing n-substituted 3-hydroxypyrazoles of formula (I), wherein R1 stands for optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, aryl or heteroaryl and R?2 and R3¿ mean hydrogen, cyano, halogen and optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, aryl or heteroaryl, by oxidizing a corresponding pyrazolidin-3-ons.
Abstract:
Substituted thiopyridines having general formula (I), wherein n means 1 or 2, R1 means chlorine, C¿1?-C3 fluoralkyl, nitro or methylsulfonyl; a non-substituted or halogen, C1-C4 - alkoxy, C1-C4 aloxycarbonyl, di- (C1-C4-alkylamino) carbonyl, cyano or nitro substituted C1-C10-Alkyl, C2-C10-alkenyl or C2-C10 alkinyl radical, a C3-C8-cycloalkyl radical or a non-substituted in the phenyl part or hydrogen, C1-C3-alkyl, C1-C3-alkoxy, trifluormethyl, cyano or nitro substituted C1-C4-alkylene phenyl, phenyl or naphthyl radical.
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?1 and R2¿, independently of each other, are hydrogen, C¿1?-C4 alkyl, C1-C4 alkyl halide or C1-C4 alkoxy; A is (i), the bond designated * being bonded to Y; R?3¿ is hydrogen, C¿1?-C4 alkyl, C1-C4 alkyl halide, phenoxy C1-C4 alkyl, C3-C6 cycloalkyl, cyano, C1-C4 alkoxy, hydroxy, halogen; R?4¿ is hydrogen, C¿1?-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 a method for producing 5-halo-2,4,6-trifluoroisophthalic acid of formula (I), wherein X represents F, Cl, Br, or I, by hydrolysis of 5-halo-2,4,6-trifluoroisophthalodinitrile of formula (II). Said invention is characterised in that in a first step, isophthalodinitrile (II) or a solution containing isophthalodinitrile (II) is reacted with a concentrated sulphuric acid at room temperature in order to form a 5-haIo-2,4,6-trifluoroisophthalodiamide of general formula (III), and is, subsequently, heated and in a second step, isophthalic acid (I) is produced after additional heating and addition of water.
Abstract:
The present invention provides a method for the for the protection of seeds from soil insects and of the resulting plant's roots and shoots from soil and foliar insects comprising contacting the seeds before sowing and/or after pregermination with a 2- cyanobenzenesulfonamide compound of the general formula (I) where the variables R to R are as defined in claim 1.
Abstract:
The present invention provides a method for the protection of seeds from soil insects and of the seedlings’ roots and shoots from soil and foliar insects comprising contacting the seeds before sowing and/ or after pregermination with a sulphonyl compound of the general formula (I) where the variables R1 to R5 are as defined in claim 1.
Abstract:
The invention relates to 2-substituted 7-amino-azolopyrimidine of formula (I), wherein substituents have the following meanings: R1 is hydrogen, halogen, cyano, alkyl, halogenalkyl, alkenyl, alkynyl, Cycloalkyl, alkoxy, alkoxyalkyl, benzyloxyalkyl, alkoxyalkenyl or akoxyalkinyl; R2 is hydrogen, halogen, cyano, alkyl, halogenalkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkoxyalkyl and alkylthioalkyl, wherein a carbon chain in R1 and/or R2 are substitutable according to a description; R3 is halogen, Cyano, NRARB, hydroxy, mercapto, alkyl, halogenalkyl, cycloalkyl, alkoxy, alkylthio, cycloalkoxy, cycloalkylthio, carboxyl, formyl, alkylcarbonyl, alkoxycarbonyl, alkenyloxycarbonyl, alkinyloxycarbonyl, phenyl, phenoxy, phe- nylthio, benzyloxy, benzylthio, alkyl-S(O)m-; A N and CRx; Rx is hydrogen or one of above groups for R3. A method and intermediate products for producing said compounds, agents containing said compounds and the use thereof for combating plant-pathogen fungi are also disclosed.