Bayer Aktiengesellschaft

Klaus Bockmann

Wilhelm Brandes

Karl H Buchel

Klaus Lurssen

Paul Reinecke

Erik Regel

Stefan Dutzmann

Gerhard Jager

Jorg Konze

Klaus Stroech

Paul-Ernst Frohberger

Hans Scheinpflug

Gerd Hanssler

Wilhelm Stendel

Manfred Plempel

Monika Frie

Plant growth-regulating and fungicidal compounds of the formula ##STR1## in which Ar represents optionally substituted aryl or optionally substituted heteroaryl,

Substituted azolylmethyl-cyclopropyl-carbional derivatives

Substituted azolylmethyl-cyclopropyl-carbinol derivatives

Hydroxyalkinyl-azolyl derivatives of the formula ##STR1## in which A is a nitrogen atom or the CH group,

Fungicidal novel hydroxyalkynyl-azolyl derivatives

Fungicidal and plant growth regulating hydroxyethylazolyl derivatives of the formula ##STR1## in which R represents hydrogen, alkyl or acyl,

Fungicidal and plant growth-regulating hydroxyethyl-azolyl derivatives

A method of combating mycoses which comprises administering to a patient in need thereof an antimycotic effective amount of an azolylcyclopropyl-azolylmethyl-carbinol derivative of the formula ##STR1## in which Ar is optionally substituted aryl or optionally substituted heteroaryl,

Antimycotic agents

Fungicidal and plant growth-regulating azolyltetrahydropyran derivatives of the formula ##STR1## in which R represents hydrogen, alkyl or acyl,

Fungicidal and plant growth-regulating azolyl-tetrahydropyran derivatives

Substituted azolylcyclopropyl-azolylmethyl-carbinol derivatives of the formula ##STR1## in which Ar is optionally substituted aryl or optionally substituted heteroaryl,

Substituted azolylcyclopropyl-azolylmethyl-carbinol derivatives

Combating Pseudocercosporella herpotrichoides by use of an azolylmethyl-cyclopropyl-carbinol derivative of the formula ##STR1## in which R.sup.1 represents fluorine or chlorine and

Use of azolylmethyl-cyclopropylcarbinol derivatives for combating

1-(2,4-Difluorophenyl)-1-(1-fluorocylopropyl)-2-(1,2,4,-triazol-1-yl)-ethan - 1-ol of the formula ##STR1## is active against Pseudocercosporella herpotrichoides and is produced by the following reaction sequence: ##STR2##

1-(2,4-Difluorophen

Pesticidally active novel azolylvinyl ethers of the formula ##STR1## in which A represents a nitrogen atom or the CH group,

Azolylvinyl ethers and pesticidal use

Fungicidally active novel cyclic azolylvinyl ethers of the formula ##STR1## in which A is a nitrogen atom or the CH group,

Growing community of inventors

Cologne, Germany

Klaus Bockmann