Basf Aktiengesellschaft

Peter Hofmeister

Christoph Kuenast

Uwe Kardorff

Hans-Juergen Neubauer

Joachim Leyendecker

Wolfgang Krieg

Rainer Buerstinghaus

Hans Theobald

Thomas Kuekenhoehner

Franz Schuetz

Eberhard Ammermann

Gisela Lorenz

Bernd Wolf

Ulrich Schirmer

Jochen Wild

Wolfgang Seppelt

Reiner Kober

Norbert Goetz

Wolfgang Reuther

Reinhard Kirstgen

Heinrich Adolphi

Wilhelm Rademacher

Siegbert Brand

Hans Ziegler

Ulf Baus

Charles W Finch

Elmar Kibler

Reinhold Stadler

Reimer G&ouml;ttsche

Rainer Burstinghaus

Winfried Zombik

Mary Elizabeth Callan

Hubert Sauter

Wolfgang Von Deyn

Franz Merger

Axel Sanner

Gerhard Wagenblast

Rainer Becker

Albrecht Harreus

Johann Jung

Volker Harries

Walter Himmele

Matthias Bratz

Rainer Seele

Ludwig Schuster

Adolf Parg

Roger G Klimesch

Karl-Heinrich Schneider

Guenter Schulz

Karl-Friedrich Jager

Christoph Nuebling

Siegfried Kersten

Ernst Hofmann

Ulrich Neumann

Linhard Sproesser

Manfred Schroeder

Stefan Mueller

Reinhard Neudert

Wolfgang Tuerk

Jacobus J DeKramer

Thomas Kuekenhoener

Uwe Kardoff

Christoph Kuenasi

Jurgen Von Der Heyde

Klaus Grossman

Hagen Hauptmann

Winfried Angerer

Hans-Jurgen Neubauer

Karl Heinrich Schneider

Synergistic growth-regulating mixture

Pesticide containing a synergistic combination of active ingredients

3(2H)-Pyridazinone derivatives of the general formula I ##STR1## where R.sup.1 is alkyl, R.sup.2 is hydrogen or alkyl, X is halogen, W is oxygen or sulfur and Z is a hetaryl-substituted isoxazolyl radical or a substituted or unsubstituted cyclohexyl or cyclopentyl radical, plant-tolerated salts thereof, processes for their manufacture, and their use as pesticides.

3(2H)-Pyridazinone derivatives and their use for controlling pests

Phenoxyalkyl-substituted heteroaromatics of the formula Ib ##STR1## where A is an unsubstituted or substituted pyridyl radical, R.sup.1 is hydrogen, halogen or C.sub.1 -C.sub.3 -alkyl, R.sup.2 is hydrogen or C.sub.1 -C.sub.4 -alkyl, and Q.sub.b is a substituted or unsubstituted heteroaromatic radical which has a five-membered ring and their use for combatting pests.

Phenoxyalkyl-substituted heteroaromatics and their use for controlling

Hydroquinone diethers of the general formula I ##STR1## where R.sup.1 is hydrogen, halogen or C.sub.1 -C.sub.6 -alkyl, A and B are each unsubstituted or substituted methylene, ethylene or propylene and X and Y are each unsubstituted or substituted hetaryl, processes for their preparation and pesticides.

Hydroquinone diethers, their preparation and their use

Methyl .alpha.-arylacrylates substituted by a heterocyclic radical and having the general formula ##STR1## where R is alkyl, alkenyl, haloalkyl, cycloalkyl, alkoxy, alkylcarbonyl, alkoxycarbonyl, halogen or aryl, the aromatic ring being unsubstituted or substituted, Het is a five-membered heteroaromatic ring which is unsubstituted or substituted and has from one to three heteroatoms, and A is ethenylene, ethylene, methyleneoxy or methylenethio, and fungicides and pesticides containing these compounds.

Methyl .alpha.-arylacrylates substituted by a heterocyclic radical and

Phenoxyalkyl-substituted heteroaromatics of the formulae Ia and Ib ##STR1## where the substituents have the following meanings: R.sup.1 C.sub.1 -C.sub.12 -alkyl, C.sub.2 -C.sub.12 -alkenyl, C.sub.2 -C.sub.12 -alkynyl, C.sub.1 -C.sub.12 -haloalkyl,

Phenoxyalkyl-substituted heteroaromatics and a method for controlling

Phenoxyalkyl-substituted heteroaromatics of the general formulae Ia and Ib ##STR1## where A is an unsubstituted or substituted heteroaromatic radical having 6 5 ring members and 1, 2 or 3 nitrogen atoms in the ring, R.sup.1 is hydrogen, halogen or C.sub.1 -C.sub.3 -alkyl. R.sup.2 is hydrogen or C.sub.1 -C.sub.4 -alkyl. Q.sub.a is an unsubstituted or substituted azole radical and Q.sub.b is a substituted or unsubstituted heteroaromatic radical which has a five-membered ring, and their use for combating pests.

N-substituted azoles of the formula I ##STR1## where R.sup.1, R.sup.2, R.sup.3 are each hydrogen, halogen, C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.3 -C.sub.10 -cycloalkyl, nitro or cyano,

N-phenoxyphenyloxymethyl substituted azoles and method for controlling

Phenoxyalkyl-substituted heteroaromatics of the general formulae Ia and Ib ##STR1## where A is an unsubstituted or substituted heteroaromatic radical having 6 ring members and 1, 2 or 3 nitrogen atoms in the ring, R.sup.1 is hydrogen, halogen or C.sub.1 -C.sub.3 -alkyl, R.sup.2 is hydrogen or C.sub.1 -C.sub.4 -alkyl, Q.sub.a is an unsubstituted or substituted azole radical and Q.sub.b is a substituted or unsubstituted heteroaromatic radical which has a five-membered ring, and their use for combating pests.

Phenoxyphenylmethyl substituted azoles and pesticidal composition thereof

Phenoxyalkyl-substituted heteroaromatics of the formulae Ia and Ib ##STR1## where the substituents have the following meanings: R.sup.1 C.sub.1 -C.sub.12 -alkyl, C.sub.2 -C.sub.12 -alkenyl, C.sub.2 -C.sub.12 -alkynyl, C.sub.1 -C.sub.12 -haloalkyl, C.sub.2 -C.sub.12 -haloalkenyl, C.sub.2 -C.sub.12 -haloalkynyl, C.sub.3 -C.sub.12 -alkoxyalkyl, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.4 -C.sub.12 -cycloalkylalkyl, C.sub.3 -C.sub.8 -halocycloalkyl, C.sub.4 -C.sub.12 -halocycloalkylalkyl, C.sub.4 -C.sub.12 -cycloalkylhaloalkyl or C.sub.4 -C.sub.12 -halocycloalkylhaloalkyl;

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Neustadt, Germany

Peter Hofmeister