Basf Aktiengesellschaft

Badische Anilin- & Soda-fabrik Aktiengesellschaft

Basf Altiengesellschaft

Walter Himmele

Eberhard Ammermann

Ernst-Heinrich Pommer

Hardo Siegel

Norbert Goetz

Rainer Becker

Ernst Buschmann

Werner Hoffmann

Hubert Sauter

Gisela Lorenz

Bruno Wuerzer

Leopold Hupfer

Rainer Seele

Dieter Jahn

Michael Keil

Wilhelm Rademacher

Hans Theobald

Johann Jung

Costin Rentzea

Heinz Eckhardt

Joachim Paust

Wolfgang Rohr

Klaus Bronstert

Reiner Kober

Gerd Steiner

Kaspar Bott

Hans-Juergen Teschendorf

Werner Aquila

Matthias Zipplies

Werner Fliege

Karl Von Fraunberg

Sigberg Pfohl

Christoph Martin

Gerhard Epple

Harald Weifenbach

Ernst Hofmann

Christiane Brueckner

Franz Merger

Klaus Hahn

Manfred Patsch

Herbert Naarmann

Wolfgang Hoelderich

Gerd Kaibel

Bernd Wolf

Christoph Kuenast

Heinrich Adolphi

Peter Hofmeister

Karl Kiehs

Adolf Echte

Juergen Hambrecht

Hansgeorg Ernst

Karl-Heinz Koenig

Herwig Hoffmann

Klaus Penzien

Franz Roehl

Ludwig Schuster

Marco Thyes

Stefan Karbach

Walter Gramlich

Rudolf Kropp

Wolfgang Mackenroth

Johann Swoboda

Wolfgang Spiegler

Karl-Heinz Ross

Lothar Janitschke

Herbert Toussaint

Kurt Schneider

Christian Dudeck

Volker Muench

Wolfgang Elser

Michael Huellmann

Karl Fischer

Gerhard Paul

Wolfgang Sauer

Walter-Wielant Wiersdorff

Rudolf Irnich

Rainer Burstinghaus

Gerald Lauterbach

Friedrich-Wilhelm Kohlmann

Wolfgang Heberle

Walter Wesenberg

Siegbert Bohnet

Rolf Lebkuecher

Reinhold Plass

Jochen Karg

Compounds of the formula I ##STR1## and of the formula II ##STR2## where R.sup.1 is unsubstituted or substituted alkyl, unsubstituted or substituted alkenyl, or alkynyl, R.sup.2 is alkyl or alkenyl and X is an acid radical, and the salts of the compounds of the formula I, and fungicides which contain these compounds.

4-(p-tert.-butylphenyl)-3-methylpiperidines substituted at the nitrogen,

Lower polyhydric alcohols are prepared by catalytic hydrogenolysis of sucrose in an aqueous solution by using a catalyst whose active material essentially consists of

Preparation of lower polyhydric alcohols

Azolylethane derivatives of the general formula I ##STR1## where A and Z are each alkyl, phenyl, biphenyl, naphthyl, benzyl, cycloalkyl or cycloalkenyl, these radicals being substituted or unsubstituted, D is alkoxy, amino, mercapto, thiophenyl, aminophenyl, hetaryloxy or phenoxy, these radicals being substituted or unsubstituted, n is an integer from 1 to 5 or 0, and X is CH or N, and their plant-tolerated acid addition salts and metal complexes, and fungicides and growth regulators containing these compounds.

Azolylethane derivatives and fungicides and growth regulators containing

1,2-Dihaloazolylethane derivatives of the general formula I ##STR1## where R.sup.1 and R.sup.2 are each substituted or unsubstituted phenyl, biphenyl, naphthyl or hetaryl, Z is chlorine or bromine, and X is CH or N, and their plant-tolerated acid addition salts and metal complexes, and fungicides and growth regulators containing these compounds.

1,2-dihaloazolylethane derivatives and crop protection agents containing

Azolylmethyloxiranes of the general formula I ##STR1## where R.sup.1, R.sup.2 and R.sup.3 are substituted or unsubstituted alkyl, benzyl, naphthyl, biphenyl, dioxanyl, phenyl, tetrahydropyranyl, tetrahydrofuranyl, norbornyl, C.sub.3 -C.sub.12 -cycloalkyl or C.sub.3 -C.sub.12 -cycloalkenyl, and X is CH or N, and plant-tolerated acid addition salts and metal complexes thereof, and fungicides containing these compounds.

Azolylmethyloxiranes and fungicides containing them

E7/Z9 -alkadien-1-ols which may be protected at the hydroxy group are prepared by subjecting a 7-hydroxyheptenal to a Wittig reaction with a phosphorylide to give an acetal compound which is converted by further Wittig reaction with a phosphorylide to an E7/Z9 -alkadienol.

Preparation of E7/Z9-alkadien-1-ols and their derivatives protected at

3-Alkyl-4-arylpyrrolidine derivatives of the formula ##STR1## where R.sup.1 is alkenyl, alkynyl, cycloalkyl, cycloalkenyl, alkyl-cycloalkyl, cycloalkyl-alkyl, alkyl-cycloalkyl-alkyl, cycloalkenyl-alkyl, alkyl-cycloalkenyl, bicycloalkyl, bicycloalkylalkyl, alkyl-bicycloalkyl, heterocycloalkyl, heterocycloalkylmethyl, aryl, arylalkyl, alkylary, alkyl-aryl-alkyl,

Fungicidal N-substituted 3-alkyl-4-arylpyrrolidine derivatives

N-Substituted 3-arylpyrrolidine derivatives of the formula ##STR1## where R.sup.1 is 2,2-dimethylpropyl, 3,3-dimethylbutyl, 4,4-dimethylpentyl, 2,4,4-trimethylpentyl, 6-methylhept-2-yl, 3,5,5-trimethylhexyl, 6,10-dimethylundec-2-yl, 3-methylcyclohexyl, 3,3-dimethylcyclohexyl, 3,3,5-trimethylcyclohexyl, 3,3,5,5-tetramethylcyclohexyl, 4-methylcyclohexyl, 4-ethylcyclohexyl, 4-propylcyclohexyl, 4-isopropylcyclohexyl, 4-tert.-butylcyclohexyl, trans-4-tert.-butylcyclohexyl, 4(2-methylbut-2-yl)cyclohexyl, 4(2,4,4-trimethylpent-2-yl)-cyclohexyl, cyclododecanyl, C.sub.3 -C.sub.9 -trialkylsilyl-substituted C.sub.4 -C.sub.12 -cycloalkyl, 4-hydroxycyclohexyl, 4-hydroxy-3-methylcyclohexyl, 4-hydroxy-3,5-dimethylcyclohexyl, 4-hydroxy-3,3-dimethylcyclohexyl, 4-hydroxy-3,3,5-trimethylcyclohexyl, unsubstituted or hydroxy-, C.sub.1 -C.sub.9 -alkyl-, C.sub.1 -C.sub.5 -alkoxy- or C.sub.3 -C.sub.9 -trialkylsilyl-substituted C.sub.5 -C.sub.12 -cycloalkenyl,

Fungicidal N-substituted 3-arylpyrrolidine derivatives

1-Halo-1-azolylethane derivatives of the formula I ##STR1## where R.sup.1 and R.sup.2 are C.sub.1 -C.sub.8 -alkyl, phenyl, biphenyl, naphthyl, benzyl, C.sub.3 -C.sub.8 -cycloalkyl or C.sub.3 -C.sub.8 -cycloalkenyl, each of which is unsubstituted or substituted,

1-halo-azolylethane derivatives and fungicides containing them

N-Arylpropyl-substituted secondary amines of the formula ##STR1## where R.sup.1 and R.sup.2 are each hydrogen, alkyl, cycloalkyl, haloalkyl, alkoxy, chlorine, bromine or fluorine, m is 0, 1 or 2, R.sup.3 and R.sup.4 are each hydrogen or alkyl, and R.sup.5 is alkyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, alkenyl or an unsubstituted or substituted phenyl or phenylalkyl radical or methylfuran and the dashed bonds may be hydrogenated, and their salts, and fungicides containing these compounds.

Propylamines, and their use as fungicides

3,9-Dihydroxynonyne and its derivatives protected at the 9-OH function, of the general formula I ##STR1## where R is hydrogen or a conventional alcohol protective group, and processes for the preparation of the compounds I.

3,9-dihydroxynonyne and its derivatives protected at the 9-OH function

Enol ethers of the general formula I ##STR1## are prepared by eliminating the radical R.sup.4 OH from acetals or ketals of the formula II ##STR2## where the substituents R.sup.1 and R.sup.2 are each independently of the other hydrogen, C.sub.1 -C.sub.12 -alkyl, C.sub.3 -C.sub.8 cycloalkyl, C.sub.3 -C.sub.8 -cycloalkenyl, unsubstituted or C.sub.1 -C.sub.4 -alkyl-substituted aryl or C.sub.7 -C.sub.16 aralkyl,

Preparation of enol ethers

Isoxazolines of the general formula II ##STR1## in which R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are each unsubstituted or halogen-, haloalkyl-, alkoxy-, haloalkoxy-, nitro-, cyano-, dialkylphosphonyl- or alkoxycarbonyl-substituted alkyl, aryl, aralkyl, alkoxycarbonyl or dialkoxyphosphonyl, R.sup.2 and R.sup.4 are each also hydrogen and R.sup.3 is also hydroxyalkyl which is unblocked or blocked by a detachable protective group or is haloalkyl, X is hydrogen or a detachable protective group, are used to prepare furans.

Isoxazolines as intermediates to furans

Preparation of 1-aryl-1-alkenes by dehydration of 1-aryl-1-alkanols in the presence of a substance promoting elimination of water, the substance being a triester of phosphorous acid in which at least one of the radicals is an aryl group. The products are suitable as, inter al., initiators for anionic polymerization.

Preparation of 1-aryl-1-alkenes

Amino compounds of the formula ##STR1## where R.sup.1 is alkyl, A is alkylene or alkenylene, and Ar is aryl, and their acid addition salts, and fungicides containing these compounds.

Amino compounds and fungicides containing them

Growing community of inventors

Walldorf, Germany

Walter Himmele