Basf Aktiengesellschaft

Basf Se Corporation

Franz Roehl

Eberhard Ammermann

Gisela Lorenz

Hubert Sauter

Bernd Mueller

Horst Wingert

Bernd Wenderoth

Hartmann Koenig

Wassilios Grammenos

Siegbert Brand

Reinhard Doetzer

Thomas Kuekenhoehner

Franz Schuetz

Matthias Zipplies

Joachim Rheinheimer

Klaus Oberdorf

Claudia Rosenbaum

Violeta Terteryan

Herbert Bayer

Wolfgang Von Deyn

Uwe Kardorff

Markus Gewehr

Christoph Kuenast

Egon Haden

Christian Harald Winter

Harald Rang

Ana Escribano Cuesta

Tobias Mentzel

Jurith Montag

Christine Wiebe

Christian Pilger

Rainer Otter

Stefan Redlich

Doris Kremzow

Sebastian Georgios Rohrer

Gerd Stammler

Doris Kremzow-Graw

Manojkumar Poonoth

Janosch Harald Achenbach

Reinharad Kirstgen

Andy Wieja

Norbert Goetz

Ernst-Heinrich Pommer

Albrecht Harreus

Walter Himmele

Bernhard Zipperer

Lothar Janitschke

Michael Hepp

The present invention relates to the use of novel oxadiazoles of the formula I or an N-oxide and/or their agriculturally useful salts for controlling phytopathogenic fungi, or to a method for combating phytopathogenic harmful fungi, which process comprises treating the fungi or the materials, plants, the soil or seeds to be protected against fungal attack, with an effective amount of at least one compound of formula I or an N-oxide or an agriculturally acceptable salt thereof; and to agrochemical compositions comprising at least one such compound and to agrochemical compositions further comprising seeds. 

Use of substituted oxadiazoles for combating phytopathogenic fungi

The present invention relates to the use of strobilurine type compounds of formula I and the N-oxides and the salts thereof for combating phytopathogenic fungi containing a mutation in the mitochondrial cytochrome b gene conferring resistance to Qo inhibitors, and to methods for combating such fungi. The invention also relates to novel compounds, processes for preparing these compounds, to compositions comprising at least one such compound, to plant health applications, and to seeds coated with at least one such compound.

Use of strobilurin type compounds for combating phytopathogenic fungi resistant to Qo inhibitors

Use of strobilurin type compounds for combating phytopathogenic fungi resistant to QO inhibitors

Carbamates and crop protection agents containing them

Carbamates of the formula I where the substituents have the following meanings:

Carbamates of the formula I ##STR1## wherein B is a saturated or unsaturated heterocyclic group, and the other substituents are defined in the specification, and having crop protection properties.

Heteroaromatic compounds of the formulae IA and IB ##STR1## where the dashed line is a double bond between the carbon atom and a Z atom, and the index and the substituents have the following meanings:

Heteroaromatic compounds and crop protection agents containing them

Heteroaromatic compounds of the formulae IA and IB ##STR1## as described in the specification, and fungicides containing these compounds.

Heteroaromatic compounds of the formulae IA and IB ##STR1## and fungicides containing these compounds.

Heteroaromatic compounds of the formulae IA and IB ##STR1## where the dashed line is a double bond between the carbon atom and a Z atom, and the index and the substituents have the following meanings: R.sup.1 alkyl, alkoxy, alkylamino R.sup.2 alkyl; A a direct bond; alkylene, alkenylene, alkynylene; O, S, S-oxides, N and alkylene derivatives or oxime radicals thereof B hydrogen, halogen, alkyl, alkenyl, alkynyl; cycloalkyl, cycloalkenyl, cycloalkynyl, heterocyclyl, aryl, hetaryl U CH.sub.2, CHCl, CHR.sup.2 or NOR.sup.2 ; X hydrogen, cyano, nitro, halogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, heterocyclyl, aryl, hetaryl; oxi- and thio derivatives thereof, carbonyl derivatives thereof, carbonyloxy derivatives thereof, amino derivatives thereof, oxime derivatives thereof, amino which may bear one or two of the abovementioned groups; m 1 or 2, Y oxygen or sulfur; Z.sup.1 -Z.sup.2, Z.sub.3 -Z.sub.4, together with the carbon atom to which they are bonded, are the radical of a heteroaromatic, and fungicides containing these compounds.

.beta.-Substituted cinnamic acid derivatives of the formula 1, ##STR1## where R.sup.1 is alkyl, chlorine or bromine, --X-- is --O--, --S--, ##STR2## m is 0 or 1, --Y is --OR.sup.4, --O--N.dbd.CR.sup.5 R.sup.6, --NR.sup.7 R.sup.8, --N(OR.sup.9)R.sup.10 or --SR.sup.11, where the above-mentioned substituents R.sup.2 to R.sup.11 are alkyl, and R.sup.2, and R.sup.3 and R.sup.5 to R.sup.11 can also be hydrogen,

.beta.-substituted cinnamic acid derivative

Oxime ether derivatives of the formula I ##STR1## where R.sup.1 and R.sup.2 are each hydrogen or alkyl, Het is pyridyl, quinolyl, pyrimidinyl, pyrazinyl, pyridazinyl, thienyl, quinoxalinyl, isoxazolyl, benzoxazolyl or benzothiazolyl bedeutet, the heterocyclic ring system being unsubstituted or substituted, and X is oxygen or sulfur, their plant-tolerated acid addition salts, metal complexes and N-oxides, and fungicides containing these compounds.

Oxime ether derivatives, their preparation and fungicides containing

Growing community of inventors

Ludwigshafen, Germany

Franz Roehl