Bayer Aktiengesellschaft

Dieter Berg

Stefan Dutzmann

Wilhelm Brandes

Wolfgang Kramer

Gerd Hanssler

Joachim Weissmuller

Paul Reinecke

Alexander Klausener

Heinz-Wilhelm Dehne

Ulrike Wachendorff-Neumann

Wolf Reiser

Thomas Seitz

Graham Holmwood

Christoph Erdelen

Winfried Lunkenheimer

Gerd Kleefeld

Klaus Lurssen

Hans-Ludwig Elbe

Manfred Jautelat

Manfred Plempel

Wilfried Paulus

Monika Frie

Peter C Knuppel

Wolfgang Kr/a/ Mer

Astrid Mauler

Robert R Schmidt

Herbert Gayer

Delf Schmidt

Ulrich Heinemann

Hans Scheinpflug

Udo Kraatz

Hermann Uhr

Arno Widdig

Detlef Wollweber

Stefan Bohm

Werner Frommer

Georg-Wilhelm Ludwig

Dietmar Schafer

Wolfgang Kr Amer

Gerd Hanbler

Joachim Weissm Uller

Fungicidally active compounds of the formula ##STR1## in which X represents oxygen or sulphur,

Intermediate for pesticidal aminomethylheterocyclic compounds

Fungicidal new 2-methoximinocarboxylic esters of the general formula (I) ##STR1## in which Ar represents one of the radicals ##STR2## and A represents one of the radicals --CH.sub.2 --; ##STR3## where Y represents one of the radicals ##STR4## --O--CH.sub.2 --; --CH.sub.2 --O--; --S--CH.sub.2 --; ##STR5## --SO.sub.2 --CH.sub.2 --; --O--; --CH.dbd.CH-- or --CH.sub.2 --CH.sub.2 --,

Fungicidal 2-methoximinocarboxylic esters

Substituted acetic acid esters of the formula ##STR1## in which R.sup.1 Represents alkyl, or represents optionally substituted aralkyl,

Substituted acetic acid esters useful as pesticides per se and as

Pesticidal aminomethylheterocyclic compounds

Fungicidal new 2-methoximinocarboxylic esters of the general formula (I) ##STR1## in which Ar represents one of the radicals ##STR2## A represents one of the radicals ##STR3## where Y represents one of the radicals ##STR4## n represents the number 0 or 1, R represents alkyl, halogenoalkyl, alkenyl, halogenoalkenyl, or represents optionally substituted cycloalkyl, or represents optionally substituted aryl or represents optionally substituted heteroaryl, and, moreover, in the event that n is 0, also represents halogen, and

New oxime ether amides of the formula (I) ##STR1## in which R has the meaning given in the description, and a plurality of processes for their preparation were described. The new oxime ether amides are used as pesticides.

Substituted oxime ether amides

Fungicidal new 2-methoximinocarboxylic esters of the general formula (I) ##STR1## in which Ar represents one of the radicals ##STR2## A represents one of the radicals --CH.sub.2 --; ##STR3## where Y represents one of the radicals ##STR4## --SO.sub.2 --CH.sub.2 --; --O--; --CH.dbd.CH-- or --CH.sub.2 --CH.sub.2 --,

Fungicidal pyridyl-substituted acrylic esters of the formula ##STR1## in which R.sup.1 represents alkyl or represents optionally substituted aralkyl,

Pesticidal pyridyl-substituted acrylic esters

Fungicidal and insecticidal substituted-heteroycylacrylic esters of the formula ##STR1## in which R.sup.1 represents alkyl, or represents unsubstituted- or substituted aralkyl,

Fungicidal and insecticidal substituted-heterocyclyl-acrylic esters

There are described new triazinyl-substituted acrylic esters of the formula (I) ##STR1## in which R.sup.1, R.sup.2, R.sup.3, R.sup.4, X and Y have the meaning given in the description, and a process for their preparation. The new acrylic esters of the formula (I) are used for the preparation of pesticides.

Triazinyl-substituted acrylic esters

Substituted oxazolidinones, some of which are known, of the formula (I) ##STR1## in which R.sup.1 to R.sup.4 have the meanings given in the description, are used for combating pests. The new compounds and those which are known can be prepared by analogous processes by reacting suitable substituted isocyanates with suitable oxiranes or by oxidising suitable oxazolidinones.

Pesticides based on substituted oxazolidinones, new substituted

Insecticidal and fungicidal substituted 2-[6-(pyrimidinyl)-indol-1-yl]-acrylic esters of the formula ##STR1## in which R.sup.1 represents alkyl, or represents optionally substituted aralkyl,

Pesticidal substituted 2-[6-(pyrimidinyl)-indol-1-yl]-acrylic esters

Fungicidal pyridinylpyrimidines of the formula ##STR1## in which R.sup.1 represents hydrogen, halogen, alkoxy, alkylthio, halogenoalkyl, amino or dialkylamino, where, in the case of dialkylamino, the two radicals may, together with the nitrogen to which they are bonded, form a 5- to 7-membered, saturated or unsaturated ring which optionally contains a further hetero atom and which is optionally substituted by 1 or 2 alkyl groups; or

Fungicidal pyridinylpyrimidines

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Wuppertal, Germany

Dieter Berg