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Manfred Jautelat

Stefan Dutzmann

Dieter Arlt

Klaus Stenzel

Gerd Hanssler

Wilhelm Brandes

Reinhard Lantzsch

Karl H Buchel

Paul Reinecke

Gerhard Jager

Wolfgang Kramer

Hans-Ludwig Elbe

Astrid Mauler-Machnik

Hans-Jochem Riebel

Heinz-Wilhelm Dehne

Rainer A Fuchs

Horst Harnisch

Stefan Hillebrand

Rolf Schroder

Klaus Stroech

Michael Schelhaas

David T Erdman

Achim Hupperts

Christoph G&uuml;rtler

Klaus Lurssen

Karl-Heinz Kuck

Ralf Tiemann

Bernd-Wieland Kr&uuml;ger

Eckart Kranz

Jorg Stetter

Helmut Fiege

Carlhans Suling

Martin Kugler

Wilfried Paulus

Dieter Berg

Jurgen Reiners

Carl Casser

Jurgen Scherkenbeck

Otto Exner

Wolf-Dieter Schroer

Monika Frie

Janos Muszik

Henning Bachem

Georg Schroder

Helmut Greiving

Astrid Mauler

Ulrike Wachendorff-Neumann

Paul-Ernst Frohberger

Manfred Plempel

Pieter Ooms

Heinrich Alberts

Hans Scheinpflug

Lutz Assmann

Dietmar Bielefeldt

Michael Ruther

Rolf Grosser

Klaus Schaller

Herbert Hugl

Manfred Dahm

Manfred Hajek

Dietmar Wastian

Rolf William Albach

Christian Laue

Klaus Ditgens

Henry Giera

Joachim Zechlin

Hanns-Peter M&uuml;ller

Fritz Mietzsch

Joachim Haider

Gerhard Arnold Braun

Katrin Joschek

Gerd Haenssler

Walter Leidinger

Gerd Hanβler

Harl-Heinz Kuck

Georg Schroeder

Heinz Dehne

Hans-Rolf Buhmann

Hans-Ferdinand Muisers

The novel active compound combinations comprising 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione of the formula and the active compound of groups (1) to (24) listed in the description have very good fungicidal properties.

Fungicide active substance combinations

A novel (&#x2212;)-enantiomer of 2-[2-(1-chloro-cyclopropyl)-3-(2-chloro-phenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione of the formula a process for preparing this novel active compound and its use as microbicide in crop protection and in the protection of materials.

(&#x2212;)-enantiomer of the 2-[2-(1-chloro-cyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione

Process for producing aliphatic tricarbonitriles

&agr;,&ohgr;-Diene metathesis in the presence of ionic liquids

The invention relates to a process for the production of 1,5-naphthalenediamine and to the intermediates 4-(2-nitrophenyl)butyronitrile, 5-nitro-3,4-dihydro-1(2H)-naphthyl-imine, 5-nitroso-1-naphthylamine, 5-nitro-1-naphthylamine, 4-(2-aminophenyl)-butyronitrile, 5-amino-3,4-dihydro-1(2H)-naphthalene imine, 4-(2-nitrophenyl)ethyl butyrate and 4-(2-nitrophenyl)butyramide obtainable during the process.

Process for the production of 1,5-naphthalenediamine

Triazolinethione-phosphoric acid derivatives

Method for production of a triazolinethione derivative

The present invention relates to additives for preparing straight-chain or acrylonitrile dimer from acrylonitrile and to a process for preparing straight-chain acrylonitrile dimer from acrylonitrile in the presence of the additives according to the invention.

Preparation of a straight-chain acrylonitrile dimer

The present invention relates to a novel process for preparing hydrazodicarbonamide (HDC) that is, after oxidation to azodicarbonamide (ADC), used industrially as a polymer auxiliary.

Process for preparing hydrazodicarbonamide via ketimines

A process for preparing aliphatic C &agr;,&ohgr;-dicarboxylic acids by oxidation of C &agr;,&ohgr;-dienes with hydrogen peroxide or compounds which release hydrogen peroxide under the reaction conditions as is characterized in that the reaction is carried out in the presence of a transition metal catalyst of group VI and of a mixture containing at least one organic acid and one aprotic organic solvent. A specific temperature profile is maintained at different phases of the reaction, which increases yield and selectivity.

Preparation of aliphatic &agr;, &ohgr;-dicarboxylic acids

The present invention relates to a process for preparing a dinitronaphthalene isomer mixture having an increased proportion of 1,5-dinitronaphthalene by nitrating naphthalene in the presence of at least one ionic liquid.

Process for preparing a dinitronaphthalene isomer mixture having an increased proportion of 1,5- dinitronaphthalene

The present invention provides the composition for novel triazolyl disulphides, the acid addition salts and metal salt complexes of the triazolyl disulphides, a process for their preparation, and a method for their use as microbicides.

Triazolyl disulphides

Growing community of inventors

Burscheid, Germany

Manfred Jautelat