Basf Aktiengesellschaft

Basfaktiengesellschaft

Basf Akdtiengesellschaft

Barbara A Schwalge

Eberhard Ammermann

Gisela Lorenz

Hubert Sauter

Bruno Wuerzer

Siegfried Strathmann

Karl Eicken

Herbert Bayer

Peter Plath

Ruth Muller

Norbert Meyer

Lothar Rueb

Karl-Otto Westphalen

Ernst-Heinrich Pommer

Ulrich Schirmer

Stefan Karbach

Wolfgang Steglich

Timm Anke

Klaus Schelberger

Reinhold Saur

Costin Rentzea

Hans J Pander

Fungicidal mixtures

Fungicidal mixtures of an oxime ether carboxylic acid amide with

Fungicidal mixtures of an oxime ether carboxylic acid amide with a

Fungicidal mixtures of an oxime ether carboxylic acid amide with an

Fungicidal mixtures of an oxime ether carboxylic acit amide with a

Fungicidal mixtures of an oximether carboxylic acid amide with

N-aryltetrahydrophthalimide compounds of the general formula I ##STR1## where is --S--C(R).sub.2 --, and a method for controlling undesirble plant growth.

N-aryltetrahydrophthalimide compounds

N-aryltetrahydrophthalimide compounds of the general formula I ##STR1## where n, R.sup.1, Y, R.sup.2 and R.sup.3 have the meanings stated in the claims and description, and a method for controlling undesirable plant growth.

N-phenyltetrahydrophthalimides of the formula I ##STR1## where R.sup.1 is hydrogen or halogen, R.sup.2 is halogen and A is a substituent of the formula ##STR2## where X is oxygen or sulfur, n is zero or one, R.sup.3 is hydrogen or C.sub.1 -C.sub.6 -alkoxycarbonyl or C.sub.1 -14 C.sub.3 -alkyl which is unsubstituted or substituted by halogen, cyano, hydroxyl, mercapto, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -alkylthio, C.sub.3 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -alkenylthio, C.sub.3 -C.sub.6 -alkynyloxy, C.sub.3 -C.sub.6 -alkynylthio or C.sub.1 -C.sub.4 -acyloxy, or is hydroxyl or carboxyl or is C.sub.1 -C.sub.4 -alkylthio-C.sub.1 - or C.sub.2 -alkyl or C.sub.1 -C.sub.4 -alkoxy-C.sub.1 - or -C.sub.2 -alkyl which is substituted in the alkyl ether or thioehter moiety by C.sub.1 -C.sub.6 -alkoxycarbonyl, R.sup.4 is hydrogen or C.sub.1 -C.sub.3 -alkyl, Z is methyleneoxymethylene, methylenethiomethylene or ethenylene (--CH.dbd.CH--) and R.sup.5 and R.sup.6 are each hydrogen or C.sub.1 -C.sub.3 -alkyl, which are useful as herbicides, are prepared.

N-phenyltetrahydrophthalimide compounds

Novel N-aryltetrahydrophthalimide compounds

3-phenylpropionic acid derivatives of the general formula I ##STR1## where R.sup.1 is hydrogen or halogen, R.sup.2 is halogen, R.sup.3 is unsubstituted or halogen-, C.sub.1 -C.sub.4 -alkoxy- or C.sub.1 -C.sub.4 -alkylthio-substituted C.sub.2 -C.sub.6 -alkyl, C.sub.5 -C.sub.7 -cycloalkyl-substituted C.sub.1 -C.sub.6 -alkyl, further C.sub.5 -C.sub.7 -cycloalkyl, C.sub.3 -C.sub.6 -alkenyl or C.sub.3 -C.sub.6 -alkynyl or, together with R.sup.4, a C.sub.2 -C.sub.4 -alkylene chain, R.sup.4 is hydrogen or unsubstituted or halogen-, C.sub.1 -C.sub.4 -alkoxy-, C.sub.1 -C.sub.4 -alkylthio- or C.sub.5 -C.sub.7 -cycloalkyl-substituted C.sub.1 -C.sub.6 -alkyl; C.sub.3 -C.sub.7 -cycloalkyl; unsubstituted or halogen-substituted C.sub.3 -C.sub.6 -alkenyl or C.sub.3 -C.sub.6 -alkynyl or halogen or R.sup.4, together with R.sup.5 and the carbon atom of this substituent, is C.sub.3 -C.sub.6 -cycloalkyl which may be interrupted by an oxygen or a sulfur atom, R.sup.5 is unsubstituted C.sub.1 -C.sub.6 -alkyl or halogen-, C.sub.1 -C.sub.4 -alkoxy- or C.sub. 1 -C.sub.4 -alkylthio-substituted C.sub.2 -C.sub.6 -alkyl; cyano or acyl (COR.sup.6) or alkoxycarbonyl (CO.sub.2 R.sup.7), R.sup.6 denoting C.sub.1 -C.sub.6 -alkyl or, together with R.sup.4, a C.sub.3 -C.sub.5 -alkylene chain and R.sup.7 denoting unsubstituted or halogen-, C.sub.1 -C.sub.4 -alkoxy- or C.sub.1 -C.sub.4 -alkylthio-substituted C.sub.2 -C.sub.6 -alkyl or unsubstituted or C.sub.5 -C.sub.7 -cycloalkyl-substituted C.sub.1 -C.sub.6 -alkyl, further C.sub.5 -C.sub.7 -cycloalkyl, C.sub.3 -C.sub.6 -alkenyl or C.sub.3 -C.sub.6 -alkynyl, with the proviso that R.sup.1 and R.sup.4 do not simultaneously denote hydrogen when R.sup.5 is cyano or CO.sub.2 R.sup.7, processes for their manufacture, and their use as herbicides.

3-phenylpropionic acid derivatives

5-(N-3,4,5,6-Tetrahydrophthalimido)-cinnamic acid derivatives of the formula Ib ##STR1## where the substituents have the following meanings: Y is chlorine, bromine or C.sub.1 -C.sub.4 -alkyl;

5-(N-3,4,5,6-tetrahydrophthalimido)cinnamic acid derivatives

N-aryltetrahydrophthalimide compounds of the general formula I ##STR1## where R.sup.1 is hydrogen or halogen, R.sup.2 is halogen, A is substituted or unsubstituted C.sub.2 -C.sub.4 -alkylene or C.sub.2 -C.sub.4 -alkenylene, B is oxygen, sulfur or a group NR.sup.3, where R.sup.3 is hydrogen or substituted or unsubstituted C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.7 -cycloalkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.2 -C.sub.6 alkenyl or C.sub.3 -C.sub.6 -alkynyl, and methods of controlling unwanted plant growth and of influencing plant growth.

N-substituted 3,4,5,6-tetrahydrophthalimide derivatives

Growing community of inventors

Lohmar, Germany

Barbara A Schwalge