Abstract:
The invention concerns 2-benzoyl-cyclohexan-1,3-diones of formula (I), in which R , R stand for hydrogen, nitro, halogen, cyano, rhodano, alkyl, halogen alkyl, alkoxyalkyl, alkenyl, alkinyl, -OR , -OCOR , -OSO2R , -SH, -S(O)nR , -SO2OR , -SO2NR R , -NR SO2R or -NR COR ; R stands for hydrogen, cyano, alkyl, halogen alkyl, -OR , -SR or -NR R ; R stands for hydrogen, optionally substituted alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkinyl, -COR , -CO2R , -COSR or -CONR R ; X stands for oxygen or NR ; n equals 0, 1 or 2; R stands for hydrogen, alkyl, halogen alkyl, alkoxyalkyl, alkenyl or alkinyl; R stands for alkyl or halogen alkyl; R stands for alkyl, halogen alkyl, alkoxyalkyl, alkenyl or alkinyl; R stands for hydrogen or alkyl; R stands for alkyl, alkenyl, alkinyl, phenyl or benzyl; R stands for alkyl, halogen alkyl, alkenyl or alkinyl; Q stands for an optionally substituted cyclohexan-1,3-dione ring linked in position 2. Also disclosed are the salts of these compounds useful in agriculture; processes and intermediate products for preparing the compounds of formula (I), agents containing the same and the use of these derivatives or agents containing the same for controlling undesirable plants.
Abstract:
The invention relates to saccharin 5 carbonyl derivatives of formula (I), wherein the substituents have the following meaning: L represents C1-C6-alkyl, C1-C6-alkoxy; Z represents C1-C6-alkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C3-C5-alkinyl, phenyl-C1-C6-alkyl or phenyl, wherein the phenyl rings are optionally substituted once or several times by C1-C6-alkyl, C1-C6-alkoxy or halogen; M represents hydrogen, C1-C6-alkyl, C1-C6-alkoxy, halogen, cyano, nitro or halogen-C1-C6-alkyl; R?1, R2, R3, R4, R5, R6, R7, R8¿ represent hydrogen, C¿1?-C6-alkyl. The invention also relates to the agriculturally usable salts of compound (I).
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.