Abstract:
The present invention relates to compounds of formula I wherein the variables are defined in the description and claims, their preparation, compositions containing compounds I, uses thereof as antifungal agents and seed coated with compounds I.
Abstract:
The invention also relates to the use of the N-acylimino heterocyclic compounds, their stereoisomers, their tautomers and their salts, for combating invertebrate pests. Furthermore the invention relates also to methods of combating invertebrate pests, which comprises applying such compounds.
Abstract:
The present invention relates to compositions of fungicidally active compounds com- prising at least one active compound I selected from 3-difluoromethyl-1-methyl-1H- pyrazole-4-carboxylic acid (3',4',5'-trifluoro-biphenyl-2-yl)-amide (fluxapyroxade), bixafen, fluopyram, isopyrazam, sedaxane, penflufen andpenthiopyrad and at least one further active component II as defined below. The invention furthermore relates to a method for controlling harmful fungi, wherein the fungi, their habitat or the plant propagation material, the soil, the plants or the materials to be protected against fungal attack are treated with an effective amount of at least one active compound I in combination with at least one active component II or with an effective amount of a composition according to the invention, to a method for protection of plant propagation material, comprising contacting the plant propagation material with an effective amount of at least one active compound I in combination with at least one active component II or with an effective amount of a composition according to the invention, to a method for protecting plants after germination from the attack of foliar phytopathogenic fungi, which comprises treating the plant propagation material from which the plants are to grow with an effective amount of at least one active compound I in combination with at least one active component II or with an effective amount of a composition according to the invention, to the use of the composition according to the invention for controlling harmful fungi, and to plant propagation material comprising the composition.
Abstract:
The invention relates to fungicidal mixtures which comprise 1) azolylmethyloxiranes of general formula I, wherein the variables are defined as in the application, and 2) a fungicidal compound II as the active components, the compounds II of component 2 being selected from among the compounds described in the application. The invention also relates to the use of the fungicidal mixtures for the control of phytopathogenic fungi and to agents containing said mixtures.
Abstract:
The present invention relates to fungicidal mixtures comprising, as active components, the fungicidal compound I and at least one further active compound as defined in the claims in synergistically effective amounts, and to a method for controlling harmful fungi using the mixtures of the compound I and the compounds II, and to the use of the compound I and the compounds Il for preparing such mixtures, and also to compositions comprising such mixtures.
Abstract:
The present invention relates to novel azole compounds of the formulae I and Il as defined below which carry a sulfur substituent, to agricultural compositions containing them, to their use as fungicides and to intermediate compounds used in the method of producing them.
Abstract:
The present invention relates to a composition, comprising a 5-amino-3-oxo-2,3- dihydro-pyrazole of the formula I as defined in the claims and the description and at least one active compound Il selected from groups A) to I) in a synergistically effective amount.
Abstract:
The present invention relates to mixtures of fungicidally active compounds comprising at least one substituted 3-hydroxymethylpyridin compound formula I and at least one further fungicidally active compound II. wherein: X is O, S or NR4; R1 is d-C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-haloalkyl, aryl-C1-C4-alkyl, aryloxy-C1-C4-alkyl, arylthio-C1-C4-alkyl, aryl or heteroaryl, wherein the cyclic moieties of the last five radicals are unsubstituted or substituted with 1, 2 or 3 radicals selected from halogen, C1-C4-alkyl, C2-C4-alkenyl, C2-C4- alkynyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-haloalkoxy, C1-C4-haloalkylthio, cyano and nitro; R2 is H or C1-C4-alkyl; R3 is C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-haloalkyl, aryl-C1-C4-alkyl, aryloxy-C1-C4-alkyl, arylthio-C1-C4-alkyl, aryl or heteroaryl, wherein the cyclic moieties of the last five radicals are unsubstituted or substituted with 1, 2 or 3 radicals selected from halogen, C1-C4-alkyl, C2-C4-alkenyl, C2-C4- alkynyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-haloalkoxy, C1-C4-haloalkylthio, cyano and nitro; R4 is H, C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-haloalkyl, aryl-C1-C6-alkyl, aryloxy-C1-C4-alkyl, arylthio-C1-C4-alkyl, aryl or heteroaryl, wherein the cyclic moieties of the last five radicals are unsubstituted or substituted with 1, 2 or 3 radicals selected from halogen, C1-C4-alkyl, C2-C4-alkenyl, C2-C4- alkynyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-haloalkoxy, C1-C4-haloalkylthio, cyano and nitro.
Abstract:
The invention relates to the triazolylmethyloxiranes of formula (I), wherein variables A, B and D have the meanings as defined in the description and the claims.
Abstract:
The present invention relates to azolyl methyl oxiranes of the formula (I), wherein the variables A, B, and D have the meanings as defined in the description and the claims.