Bayer Aktiengesellschaft

Trin Therapeutics Gmbh

Bayer Akatiengesellschaft

Heinz Forster

Robert R Schmidt

Ludwig Eue

Hans-Joachim Santel

Klaus Lurssen

Erich Klauke

Volker Mues

Hans-Joachim Diehr

Hans-Jochem Riebel

Markus Dollinger

Harry Strang

Uwe Priesnitz

Wolfgang Hofer

Fritz Maurer

Gerd Hanssler

Theodor Pfister

Klaus Wagner

Paul Reinecke

Reinhard Lantzsch

Roland Andree

Bernd Baasner

Gunther Beck

Ernst Kysela

Thomas Schmidt

Jochen Kalbe

Karl Steinbeck

Rudolf Reiter

Albrecht Marhold

Peter Dahmen

Ingeborg Hammann

Wilhelm Stendel

Wolfgang Kramer

Kurt Findeisen

Klaus-Helmut Muller

Jorg Stetter

Hermann Hagemann

Bernd Gallenkamp

Rainer A Fuchs

Wilfried Draber

Karl-Heinz Linker

Wilhelm Haas

Helmut Timmler

Johannes-Rudolf Jansen

Stefan Bohm

Karl-Rudolf Gassen

Robert H Strang

Achim Bertsch

Rolf Deege

Hans Klusacek

Arthur Wenz

Wolfgang J Hofer, Deceased

The present invention relates to novel triazene compounds, to a process for their preparation, to pharmaceutical compositions comprising them, and to the use thereof in the treatment of cancer diseases in humans. The novel triazene compounds are distinguished, as compared with the known triazene compounds, by improved activity while at the same time having reduced toxicity, that is to say by fewer side-effects.

Triazene compounds for the treatment of cancer

Herbicidal fluorothiadiazolyl oxyacetamides

Novel herbicidal active compound combinations consisting of (a) a heteroaryloxy- acetamide of the formula (I) ##STR1## in which Het represents thiadiazolyl which is substituted by halogen or by C.sub.1 -C.sub.4 -alkyl or phenyl, each of which is optionally substituted by halogen, and

Selective herbicides based on heteroaryloxy-acetamides E.G., fluthiamide

The invention relates to the use of the compound N-(4-fluoro-phenyl)-N-isopropyl-chloroacetamide of the formula (I) ##STR1## which is known, as active compound in selective herbicidal compositions, for example for combating weeds in maize cultures, and to a new process for the preparation of this active compound. The compound (I) is obtained in very high yields by reacting N-isopropyl-4-fluoro-aniline with approximately equimolar amounts of chloroacetyl chloride at temperatures between 20.degree. and 150.degree. C. in the presence of an inert diluent, such as, for example, toluene, without addition of an acid binder.

Herbicidal compositions based on

Alkyl sulphinyl and alkyl sulphonyl-1,2,4-thiadiazolyloxy acetamides and

Selective herbicides based on carbamoyltriazolinones and

Heterocyclyl-1,3,4-thiadiazolyloxyacetamides and their use as herbicides

The invention relates to the use of the compound N-(4-fluoro-phenyl)-N-isopropylchloroacetamide of the formula (I) ##STR1## which is known, as active compound in selective herbicidal compositions, for example for combating weeds in maize cultures, and to a new process for the preparation of this active compound. The compound (I) is obtained in very high yields by reacting N-isopropyl-4-fluoro-aniline with approximately equimolar amounts of chloroacetyl chloride at temperatures between 20.degree. and 150.degree. C. in the presence of an inert diluent, such as, for example, toluene, without addition of an acid binder.

Novel herbicidal fluorobenzothiazolyloxyacetamides of the formula ##STR1## in which R.sup.1 represents hydrogen or an optionally substituted radical from the group consisting of alkyl, alkenyl, alkinyl and aralkyl,

Herbicidal fluorobenzothiazolyloxyacetamides

The invention relates to novel heterocyclyltriazolinones of the general formula (I) ##STR1## in which R.sup.1 represents hydrogen, hydroxyl, cyano or alkyl, alkenyl, alkinyl, cycloalkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, arylsulphonyl, amino or heterocyclyl, each of which is optionally substituted,

Heterocyclyltriazolinones

New herbicidal fluorobenzothiazolyloxyacetamides

Herbicidal new 2-(2-benzoxazolyloxy)-acetamides of the formula ##STR1## in which R represents hydrogen, halogen, alkyl or halogenoalkyl and

Herbicidal 2-(2-benzoxazolyl-oxy)-acetamides

Herbicidal 7-chloro-benzothiazolyloxyacetamides of the formula ##STR1## in which R.sup.1 represents hydrogen or an optionally substituted radical from the series comprising alkyl, alkenyl, alkinyl or aralkyl,

Herbicidal 7-chloro-benzothiazolyloxyacetamides

Herbicidal cycloalkyl-substituted thiadiazolyloxyacetamides of the formula ##STR1## in which R.sup.1 represents hydrogen, or represents an optionally substituted radical selected from the group consisting of alkyl, alkenyl, alkynyl and aralkyl,

Herbicidal cycloalkyl-substituted thiadiazolyloxyacetamides

Growing community of inventors

Wuppertal, Germany

Heinz Forster