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Bristol-myers Squibb Compnay

Dow Agrosciences LLC

Karl-otto Westphalen

Bruno Wuerzer

Norbert Goetz

Albrecht Harreus

Karl Eicken

Joachim Rheinheimer

Gerhard Paul

Uwe Josef Vogelbacher

Eberhard Ammermann

Gisela Lorenz

Leopold Hupfer

Wolfgang Hoelderich

Thomas Kuekenhoehner

Rainer Seele

Jochen Wild

Rainer Becker

Ernst-Heinrich Pommer

Hans Theobald

Rolf Hartmuth Fischer

Norbert Meyer

Bernd Wolf

Ernst Buschmann

Bernd Zeeh

Dieter Jahn

Bernhard Zipperer

Karl-Otto Westphalen

Werner Schnurr

Michael Keil

Reiner Kober

Walter Himmele

Hubert Sauter

Peter Plath

Roman Fischer

Wolfgang Spiegler

Ulf Misslitz

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Helmut Walter

Matthias Gerber

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Ulrich Schirmer

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Stefan Karbach

Christoph Kuenast

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Gerhard Hamprecht

Thomas Zierke

Wilhelm Rademacher

Hardo Siegel

Peter Hofmeister

Dietrich Mangold

Matthias Zipplies

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Heinz Isak

Hans-Juergen Weyer

Herbert Toussaint

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Bernd Schaefer

Heinz Eckhardt

Michael Rack

Jochem Henkelmann

Uwe Kardorff

Heinrich Adolphi

Joachim Gebhardt

Joachim Leyendecker

Toni Dockner

Herbert Mueller

Werner Hoffmann

Guido Mayer

Bernd Wenderoth

Volker Maywald

Costin Rentzea

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Karl-Heinz Koenig

Kaspar Bott

Oral Aydin

Franz Roehl

Klaus Grossmann

Ludwig Schuster

Hagen Jaedicke

Klaus Halbritter

Harald Rust

Franz Schuetz

Walter Gramlich

Gernot Reissenweber

Hartmann Koenig

Dieter Degner

Gerhard Bauer

Horst Hartmann

Rolf-Dieter Kohler

Gerd Heilen

Walter Seufert

Manfred Baumann

Karl Baer

Harald Laas

Reinhard Doetzer

Wolfgang Reiss

Karin Sperling-Vietmeier

Manfred Sauerwald

Gerd Fouquet

Helmut Lermer

A method for preparing a compound of the structure I, 

Preparation of 2-amino-thiazole-5-carboxylic-acid derivatives

Process for the preparation of hydroxylamine ethers and their salts and

The use of nicotinic anilide derivatives of the general formula ##STR1## where the substituents have the following meanings: R.sup.1 halogen, methyl, trifluoromethyl, methoxy, methylthio, methylsulfinyl, methylsulfonyl

Anilide derivatives and their use for combating botrytis

Preparation of tetrahydropyran-4-carboxylic acid and its esters

Cyclohexenone oxime ethers of the general formula I ##STR1## where R.sup.1 is alkyl,

Cyclohexenone oxime ethers, their preparation, intermediates for their

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

A process for the preparation of 3-(2'-acyloxyethyl)-dihydro-2(3H)furanones of the general formula I ##STR1## in which R.sup.1 denotes C.sub.1 -C.sub.12 alkyl, C.sub.5 -C.sub.8 cycloalkyl, aryl, C.sub.7 -C.sub.12 aralkyl, or C.sub.7 -C.sub.12 alkylaryl, in which a 3-(2'-oxyethyl)-dihydro-2(3H)furanone of the general formula II ##STR2## in which R.sup.2 denotes C.sub.1 -C.sub.12 alkyl, C.sub.5 -C.sub.8 cycloalkyl, aryl, C.sub.7 -C.sub.12 aralkyl, or C.sub.7 -C.sub.12 alkylaryl is caused to react with a carboxylic acid, a carboxylic anhydride, and/or an acyl halide in the presence of an acid catalyst at temperatures of from 50.degree. to 250.degree. C. and pressures of from 0.1 to 100 bar.

Preparation of 3-(2-acyloxyethyl)-dihydro-2(3H)furanones

A process for preparing 4-dialkoxymethylpyrazoles of the formula I ##STR1## where R.sup.1 is n-alkyl,

Preparation of 4-dialkoxymethylpyrazoles

Copolymerizable oxime ethers and copolymers containing them

A process for purifying esters of tetrahydropyran-4-carboxylic acid of the formula I ##STR1## where R.sup.1 to R.sup.3 are each C.sub.1 -C.sub.4 -alkyl, and R.sup.2 and R.sup.3 are each additionally hydrogen, from mixtures produced in the reaction of butyrolactones of the formula II ##STR2## where R.sup.2 and R.sup.3 have the abovementioned meanings, and R.sup.4 is hydrogen, alkyl of 1-6 carbons or acyl of the formula --CO--R.sup.2, with alcohols of the formula R.sup.1 OH in the presence of oxide catalysts, by distillation, which entails

Purification of esters of tetrahydro-pyran-4-carboxylic acid

A process for preparing monocarboxylic esters of the general formula I ##STR1## where R.sup.1 and R.sup.2 are each hydrogen, C.sub.1 -C.sub.12 -alkyl, C.sub.3 -C.sub.8 -cyclo-alkyl acyl, aryl or C.sub.7 -C.sub.20 -aralkyl or together --(CH.sub.2).sub.n --X--(CH.sub.2).sub.m --,

Preparation of carboxylic esters

A process for preparing 4-hydroxymethyltetrahydropyran comprises reacting tetrahydrofurans of the general formula I ##STR1## where R.sup.1 is hydrogen, C.sub.1 - to C.sub.6 -alkyl or --CO--R.sup.2, and

Preparation of 4-hydroxymethyltetrahydropyran

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Worms, Germany

Norbert Goetz