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 novel triazole 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 novel triazole compounds of the formulae (I) and (II) as defined in the claims and description 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 compositions of fungicidally active compounds comprising at least one substituted pyrrole compound of formula I as defined below and at least one further fungicidally active compound II. The invention furthermore relates to a method for controlling harmful fungi, wherein the fungi, their habitat or the materials or plants to be protected against fungal attack, or the soil or propagation material are treated with an effective amount of at least one substituted pyrrole compound of formula I in combination with at least one compound II or with an effective amount of a composition according to the invention, to a method for protection of seed, comprising contacting the seeds with at least one compound of formula I in combination with at least one compound II, and to the use of the composition according to the invention for controlling harmful fungi.
Abstract:
Verbindungen der Formel I worin die Variablen die in den Ansprüchen bzw. der Beschreibung angegebenen Bedeutungen aufweisen; und deren landwirtschaftlich verträglichen Salze.
Abstract:
Die vorliegende Erfindung betrifft Verbindungen der Formel (I) worin die Variablen die in den Ansprüchen und der Beschreibung definierten Bedeutungen aufweisen.
Abstract:
Die vorliegende Erfindung betrifft Verbindungen der Formel (I) worin die Variablen die in den Ansprüchen und der Beschreibung definierten Bedeutungen aufweisen.
Abstract:
Die vorliegende Erfindung betrifft Verbindungen der Formel (I), worin die Variablen die in den Ansprüchen und der Beschreibung angegebenen Bedeutungen aufweisen.
Abstract:
Die vorliegende Erfindung betrifft Fungizide Mischungen, enthaltend als aktive Komponenten 1) Azolylmethyloxirane der allgemeinen Formel (I) worin A für Phenyl steht, das mit drei F substituiert ist, B für unsubstituiertes Pyridyl, Thienyl, Thiazolyl, Oxazolyl oder Furyl steht oder für Phenyl, das durch ein bis drei der folgenden Substituenten Halogen, NO 2 , Amino, C 1 -C 4 -Alkyl, C 1 -C 4 -Alkoxy, C 1 -C 4 -Halogenalkyl, C 1 -C 4 -Halogenalkoxy, C 1 -C 4 -Alkylamino, C 1 -C 4 -Dialkylamino, Thio oder C 1 -C 4 -Alkylthio substituiert ist, sowie deren für Pflanzen verträgliche Säureadditions-oder Metallsalze, und 2) eine fungizide Verbindung II wie in der Anmeldung beschrieben, die Verwendung der fungiziden Mischungen zur Bekämpfung von pflanzenpathogenen Pilzen und sie enthaltende Mittel.
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; R 1 is d-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, aryl-C 1 -C 4 -alkyl, aryloxy-C 1 -C 4 -alkyl, arylthio-C 1 -C 4 -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, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 - alkynyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkoxy, C 1 -C 4 -haloalkylthio, cyano and nitro; R 2 is H or C 1 -C 4 -alkyl; R 3 is C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, aryl-C 1 -C 4 -alkyl, aryloxy-C 1 -C 4- alkyl, arylthio-C 1 -C 4 -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, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 - alkynyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkoxy, C 1 -C 4 -haloalkylthio, cyano and nitro; R 4 is H, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, aryl-C 1 -C 6 -alkyl, aryloxy-C 1 -C 4 -alkyl, arylthio-C 1 -C 4 -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, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 - alkynyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkoxy, C 1 -C 4 -haloalkylthio, cyano and nitro.