Basf Aktiengesellschaft

Wolfgang Krieg

Uwe Kardorff

Christoph Kuenast

Peter Hofmeister

Joachim Leyendecker

Hans-Juergen Neubauer

Hans Theobald

Ernst Buschmann

Christoph Nuebling

Ulrich Neumann

Reinhard Kirstgen

Wolfgang Reuther

Thomas Kuekenhoehner

Ulf Baus

Wolfgang Mackenroth

Ulrich Klein

Rainer Becker

Hansgeorg Ernst

Rainer Buerstinghaus

Walter Seufert

Wolfgang Seppelt

Gregor Schuermann

Guenter Renz

Wittko Francke

Christiane Mackenroth

Reinhard Neudert

Jacobus J DeKramer

Roland Milli

Mechtild Meiwald

Hagen Hauptmann

Jacobus Jan De Kramer

Wolf Engels

Uwe Kardoff

Christoph Kuenasi

The use of terpenes for reducing the pheromone action on Lepidoptera and a method which allows terpenes to act on the habitat of the Lepidoptera are described.

Terpenes for reducing the effect of pheromone on lepidoptera

A process for preparing a mixture of 8E,10E-dodecadienol (Ia), 8E,10Z-dodecadienol (Ib), 8Z,10E-dodecadienol (Ic) and 8Z,10Z-dodecadienol (Id),

Preparation, intermediates for the preparation and the use of a mixture

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

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.

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.

Hydroquinone diethers of the formula I ##STR1## where A.sup.1 and A.sup.2 are substituted or unsubstituted alkylene;

Hydroquinone diethers, compounds which are useful for controlling pests

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;

Cyclopropane(thio)carboxamides of the general formula I ##STR1## where the index and the substituents have the following meanings: n is 0, 1 or 2, it being possible for the R.sup.2 radicals to be different when n is 2;

Cyclopropane(thio)carboxamides, the preparation thereof and

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-menbered ring, and their use for combating pests.

Novel substituted N-hydroxypyrazoles or N-hydroxytriazoles of the general formula I ##STR1## where X and Y are O, S, SO, SO.sub.2 or CH.sub.2, B is N-pyrazolyl or N-1,2,4-triazolyl of the formulae Ba and Bb respectively ##STR2## R.sup.1 and R.sup.2 are hydrogen or C.sub.1 -C.sub.3 -alkyl, R.sup.3 is hydrogen, halogen or C.sub.1 -C.sub.3 -alkyl, z is 1, 2 or 3, R.sup.4, R.sup.5 and R.sup.6 are hydrogen, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl or C.sub.1 -C.sub.4 -haloalkoxy, and n is 0, 1 or 2, and methods of combating pests.

Substituted N-hydroxypyrazoles and N-hydroxytriazoles for controlling

Cyclopropanecarboxyamides of the general formula I ##STR1## Where R.sup.1 is C.sub.1 -C.sub.4 -alkyl, fluorine, chlorine, bromine, C.sub.1 -C.sub.3 -haloalkyl or C.sub.1 -C.sub.3 -haloalkoxy, R.sup.2 is hydrogen, fluorine, chlorine or bromine, with the proviso that R.sup.1 is not fluorine if R.sup.2 is H, and pesticides containing these compounds.

Specifically substituted cyclopropanecarboxamides and their use for

Cyclopropanethiocarboxamides I ##STR1## (R.sup.1, R.sup.2 =H, CN, NO.sub.2, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -haloalkoxy; R.sup.3, R.sup.4 =H, C.sub.1 -C.sub.4 -alkyl; n=0 or 1). The compounds I are suitable as pesticides.

Growing community of inventors

Weingarten, Germany

Wolfgang Krieg