Basf Aktiengesellschaft

Basf Aktiengesellschaft, Patentabteilung

Vase Aktiengesellschaft

Johann Jung

Wilhelm Rademacher

Bernd Zeeh

Hubert Sauter

Bruno Wuerzer

Eberhard Ammermann

Ulrich Schirmer

Dieter Kolassa

Michael Keil

Costin Rentzea

Norbert Meyer

Ernst Buschmann

Dieter Jahn

Norbert Rieber

Rolf Platz

Gisela Lorenz

Rainer Seele

Werner Fuchs

Reiner Kober

Juergen Kast

Ulf-Rainer Samel

Norbert Goetz

Rainer Becker

Hans Theobald

Karl Kiehs

Guenter Schulz

Karl-Otto Westphalen

Ernst-Heinrich Pommer

Walter Himmele

Gerd Heilen

Albrecht Harreus

Wolfgang Rohr

Klaus Grossmann

Stefan Karbach

Wolfgang Spiegler

Karl-Heinz Feuerherd

Wolfgang Will

Juergen Schubert

Eberhard P Schott

Linhard Sproesser

Jens-Uwe Bliesener

Volker Fischer

Henning Rosebrock

Wolfgang Tuerk

Karl Eicken

Joachim Rheinheimer

Ulf Misslitz

Peter Plath

Helmut Hagen

Werner Hoffmann

Peter Hofmeister

Bernd Wenderoth

Hansgeorg Ernst

Lothar Rueb

Rolf-Dieter Kohler

Bernhard Zipperer

Thomas Saupe

Manfred Baumann

Winfried Richarz

Heinz Eckhardt

Gerhard Paul

Juergen Markert

Guenter Retzlaff

Manfred Lauer

Dale R Carlson

Vilmos Czikkely

Karl Roeser

Bernhard Hesse

Hansjoerg Fritsch

Walter Von Maessenhausen

Max Luib

Akihide Watanabe

Klaus Grosmann

Klaus Grossman

Wilheim Rademacher

Tetrahydropyran-2,4-diones of the formula ##STR1## where R.sup.1 is hydrogen; C.sub.1 -C.sub.6 -alkyl; C.sub.2 -C.sub.6 -alkenyl; C.sub.2 -C.sub.6 -alkynyl; substituted or unsubstituted phenyl; C.sub.1 -C.sub.6 -alkylsulfonyl; substituted or unsubstituted benzenesulfonyl; C.sub.3 -C.sub.6 -alkenylcarbonyl; or substituted or unsubstituted benzoyl; R.sup.2 is C.sub.1 -C.sub.6 -alkyl; C.sub.2 -C.sub.6 -alkenyl; C.sub.2 -C.sub.6 -alkynyl; C.sub.1 -C.sub.6 -haloalkyl; or C.sub.3 -C.sub.6 -cycloalkyl; A, B and D are each .dbd.CH-- or .dbd.N--; E is oxygen, sulfur or --NR.sup.7 --. R.sup.7 is hydrogen; C.sub.1 -C.sub.6 -alkyl; C.sub.2 -C.sub.6 -alkenyl; C.sub.2 -C.sub.6 -alkanoyl; substituted or unsubstituted benzoyl; benzyl; or substituted or unsubstituted phenyl; X is halogen; C.sub.1 -C.sub.6 -alkyl; substituted or unsubstituted C.sub.3 -C.sub.6 -cycloalkyl; C.sub.2 -C.sub.6 -alkenyl; C.sub.2 -C.sub.6 -alkynyl; C.sub.1 -C.sub.6 -alkoxy; C.sub.2 -C.sub.6 -alkenyloxy; C.sub.1 -C.sub.6 -alkylthio; C.sub.1 -C.sub.6 -alkoxycarbonyl; C.sub.2 -C.sub.6 -alkanoyloxy; substituted or unsubstituted benzyloxy; substituted or unsubstituted NR.sup.5 R.sup.6 ; formyl; C.sub.2 -C.sub.6 -alkanoyl or its imine, oxime or Schiff's base; or substituted or unsubstituted phenyl; n is 0, 1 or 2; R.sup.3, R.sup.4, R.sup.5 and R.sup.6 are each hydrogen, C.sub.1 -C.sub.6 -alkyl, phenyl, C.sub.2 -C.sub.6 -alkanoyl, benzoyl and/or benzyl; Z is oxygen or --NOR.sup.8 ; and R.sup.8 is substituted or unsubstituted C.sub.1 -C.sub.6 -alkyl; C.sub.2 -C.sub.6 -alkenyl; C.sub.2 -C.sub.6 -alkynyl; C.sub.2 -C.sub.6 -haloalkynyl; or substituted or unsubstituted thenyl; their environmentally compatible salts, and agents containing them.

Herbicidal tetrahydropyran-2,4-diones

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

Cyclohexenone derivatives of the formula ##STR1## where R.sup.1, R.sup.2, R.sup.3, Y and Z have the meanings given in the disclosure, processes for their manufacture, herbicidal and growth-regulating agents containing the novel active ingredients, and processes for combating unwanted plant growth and for regulating plant growth.

Cyclohexenone derivatives, their preparation and their use as herbicides

Vinylazoles of the general formula I ##STR1## where R.sup.1 and R.sup.2 are alkyl, cycloalkyl, tetrahydropyranyl, pyridyl, naphthyl, biphenyl or phenyl, these radicals being substituted or unsubstituted, X is CH or N, and plant-tolerated acid addition salts and metal complexes thereof, and crop protection agents containing these compounds.

Vinylazoles and the use thereof for crop protection

Cyclohexenone compounds of the formula I ##STR1## where the substituents have the following meanings: R.sup.1 substituted or unsubstituted alkyl, alkenyl, alkynyl, cycloalkyl, phenyl or benzyl;

Cyclohexenone compounds and their use as herbicides or plant growth

1-Halovinylazoles of the general formula I ##STR1## where A and R are each alkyl, cycloalkyl, cycloalkenyl, pyridyl, tetrahydropyranyl, naphthyl, biphenyl or phenyl, each of these radicals being substituted or unsubstituted, D is chlorine or bromine, and X is CH or N, acid addition salts and metal complexes thereof which are tolerated by plants, and fungicides and growth regulators containing these compounds.

1-halovinylazoles and fungicides and growth regulators containing these

Cyclohexenone derivative of the formula ##STR1## where A is oxygen or NOR.sup.8, where R.sup.8 is alkyl, alkenyl, alkynyl, haloalkyl or haloalkenyl, chlorothienyl or alkoxyalkyl

Cyclohexenone derivatives, preparation and use thereof as herbicides

##STR1## where A is C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -cycloalkenyl or tetrahydropyranyl, each of which is unsubstituted or mono- to trisubstituted by halogen, nitro, phenoxy, amino, alkyl or haloalkyl having 1 to 4 carbon atoms in each case, and X is N, and their acid addition salts and metal complexes which are tolerated by plants, and fungicides and growth regulators containing these compounds.

Azolylethylcyclopropanes and their use thereof as crop protection agents

Salicyclic acid derivatives and their sulfur analogs of the formula I ##STR1## where R.sup.1 to R.sup.5, X, Y and Z have the meanings given in the disclosure and claims, agents containing the salicyclic acid derivatives, and their use as herbicides.

Salicylic acid derivatives and their sulfur analogs

Cyclohexenone compounds of the formula I ##STR1## wherein R.sup.1, R.sup.2, A and X have the meanings given in the disclosure and claims, their preparation and their use as growth-regulating agents or herbicides.

Cyclohexenone compounds and use as herbicides or as plant growth

Azolylmethylcyclopropanes of the formula ##STR1## where R is alkyl, cycloalkyl, cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, and these radicals are substituted or unsubstituted, A is H, F, Cl or Br, and X is CH or N, their plant-tolerated acid addition salts and metal complexes, and fungicides and growth-regulating agents containing these compounds.

Azolylmethylcyclopropanes and their use as crop protection agents

Triazole compounds of the formulae Ia and Ib ##STR1## where R.sup.1 is hydrogen or cyclopropyl, or is C.sub.1 -C.sub.4 -alkyl, C.sub.2 -C.sub.4 -alkenyl or C.sub.2 -C.sub.4 -alkynyl, each of which is unsubstituted or substituted by methyl, ethyl, ethenyl, ethynyl, hydroxyl, fluorine, chlorine, bromine or C.sub.1 -C.sub.4 -alkoxy, or is C.sub.1 -C.sub.4 -alkoxy, C.sub.2 -C.sub.4 -alkenyloxy or C.sub.2 -C.sub.4 -alkynyloxy,

Triazole compounds and methods for regulating plant growth

Agents for regulating plant growth containing an effective amount of at least one cyclohexenone derivative of the formula ##STR1## where R.sup.1, R.sup.2 and R.sup.3 have the meanings given in the disclosure, or a salt thereof, and a process from regulating plant growth.

Agents for regulating plant growth

Azetidine derivatives of the formula I ##STR1## where R.sup.1 and R.sup.2 are each hydrogen or C.sub.1 -C.sub.3 -alkyl, A is --XR.sup.3 or --N(R.sup.5)--OR.sup.4, X is oxygen or sulfur, R.sup.3 is C.sub.1 -C.sub.20 -alkyl, C.sub.1 -C.sub.20 -haloalkyl, C.sub.3 -C.sub.18 -alkenyl, C.sub.3 - or C.sub.4 -alkynyl, bridged C.sub.3 -C.sub.12 -cycloalkyl or C.sub.4 -C.sub.12 -alkylcycloalkyl, the cycloalkyl radicals or alkylcycloalkyl radicals being unsubstituted or substituted by C.sub.1 -C.sub.5 -alkyl or cyclohexyl, R.sup.4 is C.sub.1 -C.sub.20 -alkyl, C.sub.1 -C.sub.12 -haloalkyl, C.sub.1 -C.sub.6 -cyanoalkyl, C.sub.1 -C.sub.12 -alkoxyalkyl, C.sub.3 -C.sub.18 -alkenyl, C.sub.3 -C.sub.18 -haloalkenyl, C.sub.3 - or C.sub.4 -alkynyl, C.sub.3 -C.sub.12 -cycloalkyl or C.sub.4 -C.sub.12 -cycloalkylalkyl, C.sub.3 -C.sub.16 -alkoxycarbonylalkyl or unsubstituted or substituted C.sub.7 -C.sub.20 -aralkyl and R.sup.5 is hydrogen or C.sub.1 -C.sub.3 -alkyl, and agents and methods for regulating plant growth.

Azetidine derivative and their use for regulating plant growth

Growing community of inventors

Limburgerhof, Germany

Johann Jung