Cl Pharma Aktiengesellschaft

Chemie Linz Aktiengesellschaft

Hafslund Nycomed Pharma Aktiengesellschaft

Gerald Saischek

Karl Schermanz

Kurt Martetschlager

Dietmar Kores

Josef Graf

Gerhard Haas

Robert Urmann

Karlheinz Wegleitner

Ferdinand Heu

Roman Wohlmuth

Hans Bodingbauer

Allylaminoethyltriazoles of the formula: ##STR1## in which R is a hydrogen atom or an alkyl group containing 1 to 5 carbon atoms; each of Ar and Ar' is an unsubstituted phenyl group, a phenyl group substituted by one or more substituents selected from C.sub.1 -C.sub.3 alkyl, C.sub.1 -C.sub.3 alkoxy, nitro and halogen, an unsubstituted thienyl group, or a thienyl group substituted by halogen or naphthyl; phytophysiologically or pharmacologically tolerated acid addition salts thereof; and fungicidal and antimycotic agents containing such compounds.

Allylaminoethyltnazoles as fungicides and antimycotic agents

New allylaminoethylimidazoles of the formula: ##STR1## in which R is a hydrogen atom or an alkyl group containing 1 to 5 carbon atoms; each of Ar and Ar' is an unsubstituted phenyl group, a phenyl group substituted by one or more substituents selected from C.sub.1 -C.sub.3 alkyl, C.sub.1 -C.sub.3 alkoxy, nitro and halogen, an unsubstituted thienyl group, or a thienyl group substituted by halogen or naphthyl; phytophysiologically or pharmacologically tolerated acid addition thereof; and fungicidal and antimycotic agents containing such compounds.

Allylaminoethylazoles

New imidazole derivatives of the formula ##STR1## in which Ar denotes phenyl, biphenylyl, naphthyl or thienyl, each of which is optionally substituted by halogen, lower alkyl or lower alkoxy, R.sub.1 denotes hydrogen or lower alkyl, Alk denotes straight-chain or branched alkylene having 1 to 10 carbon atoms, Y denotes oxygen, sulfur, sulfinyl or sulfonyl, n denotes one of the numbers 0, 1 or 2, Z denotes sulfur or sulfinyl, m denotes the number 0 or 1, m being the number 0 when Y denotes sulfur, sulfinyl or sulfonyl, and m being the number 1 when Y denotes oxygen, and R.sub.2 denotes cyclohexyl, phenyl or naphthyl, each of which is optionally substituted by hydroxyl, halogen, trifluoromethyl, lower alkyl or lower alkoxy, or denotes biphenylyl or pyridyl, and processes for their preparation. The imidazole derivatives have excellent antimycotic properties for use in human and veterinary medicine.

Imidazole derivatives and antimycotics containing them

Imidazole and triazole derivatives of the general formula ##STR1## in which Ar denotes thienyl or denotes phenyl, biphenylyl or naphthyl, each of which is substituted by halogen, lower alkyl or lower alkoxy, R.sub.1 denotes hydrogen or lower alkyl, Alk denotes straight-chain or branched alkyl having 1 to 10 carbon atoms, Y denotes oxygen, sulfur, sulfinyl or sulfonyl, n denotes zero, 1 or 2, Z denotes oxygen, sulfur or sulfinyl, m denotes zero or 1, R.sub.3 denotes hydrogen, straight-chain or branched alkyl, cyclohexyl, or denotes phenyl which is optionally substituted by hydroxyl, halogen, trifluoromethyl, lower alkyl or lower alkoxy, or denotes biphenlyl, pyridyl or denotes naphthyl which is optionally substituted by halogen, X denotes CH or N, and R.sub.2 denotes hydrogen or lower alkyl, and their pharmaceutically acceptable acid addition salts for use as antimycotic agents in human and veterinary medicine.

Triazole derivatives for use as antimycotic agents

Novel 1,3,2-dioxaborinanes of the general formula ##STR1## wherein R.sub.1 is a straight-chain or branched alkyl group having 1 to 20 carbon atoms, a phenyl group or bromine, Y is a 1-oxy-2-thioethyl group, a 1-oxy-4-thiophenyl group or oxygen, each group Z independently of the others is a straight-chain or branched alkyl group having 1 to 20 carbon atoms, a cycloalkyl, bicycloalkyl or cycloalkylalkyl group, a phenyl group or a phenylalkyl radical, and n is the number 1 or 2. The compounds possess outstanding biocidal properties.

1,3,2-dioxaborinanes

Novel spirocyclic boron compounds of the formula ##STR1## in which R.sub.1 and R.sub.2 are various halogen containing organic :radicals and Z.sup.+ is a hydrogen ion, an equivalent of an alkaline-earth metal ion, a guanidinium ion or alkylammonium ion as flame retarding agents in various plastics, such as polyurethanes, epoxide resins and polyesters.

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Lannach, Austria

Gerald Saischek