Abstract:
The invention concerns pyrazolylhetaroyl derivatives of formula (I) in which the substituents have the following meanings: L, M are hydrogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkinyl, C1-C4 alkoxy, wherein these groups can optionally be substituted by between one and five halogen atoms or C1-C4 alkoxy; halogen, cyano, nitro; X is oxygen or sulphur which can be substituted by one or two oxygens; n is zero, one, two; and Q, R?1, R2, R3, R4¿ have the meanings given in claim 1. The invention further concerns a process for preparing the pyrazole-4-yl-hetaroyl derivatives, agents containing the latter, and the use of these derivatives or agents containing them for weed control.
Abstract:
The invention relates to pyrazoles of formula (I) wherein said variables can represent the following: R1 = hydrogen, nitro, halogen, cyano, rhodano or an aliphatic radical; R2 = a substituted sulphur, nitrogen or phosphor atom; R3 = hydrogen, halogen or an alliphatic radical; R4, R5 = hydrogen, nitro, halogen, cyano, rhodano ar an aliphatc radical; R6 = hydrogen, halogen, C¿1?-C6-alkyl, C1-C6-alkoxy, C3-C8-cycloalkyl; R?7, R8, R9¿ = hydrogen, C¿1?-C6-alkyl, whereby at the most R?7, R8, R9¿ represent hydrogen; in addition to the tautomers and agriculturally useful salts thereof. The invention also relates to methods for the production of compounds of formula (I), agents containing said compounds, the use of compounds of formula (I) and agents containing said compounds as pesticides.
Abstract:
The invention relates to cyclohexenone derivatives of benzo-condensed, unsaturated 5-ring nitrogen heterocycles of general formula (I) wherein X represents N or a group C-R3, Y represents O, S, SO, SO¿2? or NR?4¿ or X-Y represent S=N and X represents sulfur, and the variables R1, R2 and Hex have the meanings given in claim 1. The invention also relates to a method for producing these compounds, to agents containing these compounds, and to their use as herbicides.
Abstract:
The invention concerns 3-(4-cyanophenyl)uracils of formula (I), wherein A = H, CH3, NH2; Y = -O-, -S-; R1 = H, halogen; R2 = H, halogen, C¿1?-C6-alkyl, C1-C6-alkyl halide, C1-C6-alkylthio, C1-C6-alkylsulphenyl, C1-C6-alkylsulphonyl; R?3¿ = H, halogen, C¿1?-C6-alkyl; R?4¿ = H, C¿1?-C6-alkyl halide, C1-C6-alkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C3-C6-alkinyl, (C1-C6-alkyl)carbonyl, (C3-C6-alkenyl)carbonyl, (C3-C6-alkinyl)carbonyl or alkylsulphonyl, each of the last-mentioned eight groups being able to carry one to three substituents: halogen, nitro, cyano, hydroxy, C3-C8-cycloalkyl, C1-C6-alkoxy, C3-C8-cycloalkoxy, C3-C6-alkenyloxy, C3-C6-alkinyloxy, C1-C6-alkoxy-C1-C6-alkoxy, C1-C6-alkylthio, C1-C6-alkylsulphenyl, C1-C6-alkylsulphonyl, C1-C6-alkylidene aminoxy, optionally substituted phenyl, phenoxy or phenylsulphonyl, an optionally substituted 3 to 7-member heterocyclyl or heterocyclyloxy group with one to three heteroatoms, -CO-XR?5¿, -OCO-XR5 or -N(R5)R6, wherein X = chemical bond, oxygen, sulphur or -N(R6)-; R5 = H, C¿1?-C6-alkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C3-C6-alkinyl, C1-C6-alkoxy-C1-C6-alkyl, (C1-C6-alkoxy)carbonyl-C1-C6-alkyl, optionally substituted phenyl or phenyl-C1-C6-alkyl; or X and R?5¿ together equal a 3 to 7-member heterocyclic ring which is bonded via nitrogen, has one to three heteroatoms and can optionally carry one to three substituents; R6 = H, OH, C¿1?-C6-alkyl, C3-C8-cycloalkyl or C1-C6-alkoxy, and the salts of I when A = hydrogen. The products are used as herbicides, for desiccating and defoliating plants.
Abstract:
The invention relates to substituted 2-phenylpyridines (I) and their salts, and to the use thereof as herbicides for the desiccation/defoliation of plants.
Abstract:
The invention concerns substituted 2-phenylpyridines of formula (I) and their salts, in which X = a bond, 1,2-ethinediyl, an optionally substituted methylene-, 1,2-ethanediyl- or 1,3-propylene bridge, optionally substituted methyleneoxymethylene, methylenethiamethylene, ethene-1,2-diyl, optionally substituted oxymethylene, thiamethylene, oxyethylene or thiaethylene bonded to the phenyl ring via the heteroatom; Y = -O-, -S-; -Z = -O-, -S-, -N(R )-; Z = -O2-, -S-, -N(R )-; R , R , R , R = H, C1-C6-alkyl, C1-C6-alkyl halide, hydroxy-C1-C4-alkyl, cyano-C1-C4-alkyl, C1-C4alkoxy-C1-C4alkyl, C1-C4alkoxy halide-C1-C4-alkyl, C3-C4-alkenyloxy-C1-C4-alkyl, C3-C4-alkinyloxy-C1-C4-alkyl, C3-C8-cycloalkoxy-C1-C4-alkyl, amino-C1-C4-alkyl, C1-C4-alkylamino-C1-C4-alkyl, di-(C1-C4-alkyl)amino-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-alkylthiohalide-C1-C4-alkyl, C3-C4-alkenylthio-C1-C4-alkyl, C3-C4alkinylthio-C1-C4-alkyl, C1-C4-alkylsulphinyl-C1-C4-alkyl, C1-C4-alkylsulphinylhalide-C1-C4-alkyl, C3-C4-alkenylsulphinyl-C1-C4-alkyl, C3-C4-alkinylsulphinyl-C1-C4-alkyl, C1-C4-alkylsulphonyl-C1-C4-alkyl, C1-C4-alkylsulphonyl halide-C1-C4-alkyl, C3-C4-alkenylsulphonyl-C1-C4-alkyl, C3-C4-alkinylsulphonyl-C1-C4-alkyl, C3-C6-alkenyl, C3-C6-alkenyl halide, cyano-C3-C6-alkenyl, C3-C6-alkinyl, C3-C6-alkinyl halide, cyano-C3-C6-alkinyl, hydroxycarbonyl-C1-C4-alkyl, (C1-C4-alkoxy)-carbonyl-C1-C4-alkyl, (C1-C4-alkylthio)carbonyl-C1-C4-alkyl, amino-carbonyl-C1-C4-alkyl, (C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, di-(C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, optionally substituted C3-C8-cycloalkyl, C3-C8-cycloalkyl-C1-C4-alkyl, phenyl, phenyl-C1-C4-alkyl, 3- to 7-members heterocyclyl or heterocyclyl-C1-C4-alkyl, wherein all the heterocycles can contain a (thio)carbonyl ring member, or R + R and/or R + R and/or R + R together in each case are an optionally substituted 1,2-ethanediyl-, 1,3-propylene-, tetramethylene-, pentamethylene- or ethyleneoxyethylene chain; or R + R together are optionally substituted 1,2-phenylene; R = CN, halogen, C1-C4-alkyl, C1-C4 alkyl halide, C1-C4 alkoxy or C1-C4 halkoxy halide; R , R are H, halogen; R is halogen, C1-C4 alkyl halide; and n = 0,1. The invention further concerns the use of these substances as herbicides and for desiccating/defoliating plants.
Abstract:
The invention relates to a method for producing anellated triazoles, according to which substituted N-aminoureas are reacted with formaldehyde or paraformaldehyde to obtain the corresponding methylene-imine compounds and these are then cyclized in the presence of catalytic quantities of acid or in the presence of a metal oxide to tetrahydro-4H-1,3,4-ox(or thia)diazines, after which the anellated triazoles are prepared using phosgene or a phosgene substitute. The invention also relates to new anellated triazoles obtained using the method provided for by the invention.
Abstract:
The invention concerns saccharine derivatives of the formula (I) in which the substituents are defined as follows: L, M hydrogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkylthio, chlorine, cyano, methylsulphonyl, nitro or trifluoromethyl; Z hydrogen, C1-C4 alkyl, C3-C8 cycloalkyl, C3-C6 alkenyl, C3-C5 alkinyl, C1-C4 acyl, benzyl or phenyl, wherein any of the phenyl rings may be substituted by halogen or C1-C4 alkyl; R1 cyclopropyl, 1-methylcyclopropyl, 1-methylthiocyclopropyl or tert.-butyl. The invention also concerns salts of such compounds usually used in agriculture.