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Lothar Rueb

Karl Eicken

Bruno Wuerzer

Karl-Otto Westphalen

Peter Plath

Norbert Meyer

Barbara A Schwalge

Rainer Seele

Peter Schaefer

Bernd Schaefer

Eberhard Ammermann

Gisela Lorenz

Helmut Walter

Matthias Gerber

Wolfgang Rohr

Wilhelm Rademacher

Johann Jung

Reiner Kober

Bernd Zeeh

Stefan Karbach

Gernot Reissenweber

Bernhard Zipperer

Klaus Fischer

Hans J Pander

Abstract of the Disclosure: Styrene derivatives I ##STR1## where R.sup.1 is H or halogen, R.sup.2 is halogen, R.sup.3 is H, halogen or C.sub.1 -C.sub.4 -alkyl, R.sup.4 is CN or C.sub.1 -C.sub.6 -alkylcarbonyl and A is a heterocyclic radical A.sub.1 to A.sub.5 : ##STR2## where R.sup.5 and R.sup.6 are H, CH.sub.3 or C.sub.2 H.sub.5, n is 0 or 1 and X is oxygen or sulfur, with the proviso that R.sup.4 is alkylcarbonyl when R.sup.1 is H and at the same time A is A.sub.2 where n is 0, and agriculturally useful salts thereof, processes for the preparation of the styrene derivatives I and herbicides containing them.

Styrene derivatives useful as herbicides and defoliants

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

Process for making 3,4,5,6-tetrahydrophthalimide derivatives

Cinnamic esters of the formula I ##STR1## where the dotted bond is a single or double bond, R.sup.1 is hydrogen or fluorine, R.sup.2 is halogen, R.sup.3 is hydrogen, halogen or C.sub.1 -C.sub.4 -alkyl, R.sup.4 is hydrogen, substituted or unsubstituted C.sub.1 -C.sub.6 -alkyl, or is C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl or benzyl, and X is oxygen or sulfur, processes for their manufacture, and agents containing them.

Cinnamic esters

3-(N-3,4,5,6-Tetrahydrophthalimido)-cinnamic esters of the general formula I ##STR1## where n is 1 or 2 and the substituents have the following meanings:

Herbicidal 3-(3,4,5,6-tetrahydrophthalimido)-cinnamic esters

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-(Phenyl)-tetrahydroindazole derivatives of the general formula Ia and Ib ##STR1## where R.sup.1 is halogen;

Tetrahydroindazoles with a phenyl ether structures, herbicidal

N-aryltetrahydrophthalimides and herbicidal compositions thereof

Vinylazoles of the general formula I ##STR1## where R.sup.1 and R.sup.2 are alkyl, cycloalkyl, tetrahydropyranyl, pyridyl, naphthyl, biphenyl or phenyl, these radicals being substituted or unsubstituted, X is CH or N, and plant-tolerated acid addition salts and metal complexes thereof, and crop protection agents containing these compounds.

Vinylazoles and the use thereof for crop protection

N-(Phenyl)-tetrahydroindazole derivatives of the general formula 1a and 1b ##STR1## where R.sup.1 is halogen;

Tetrahydroindazoles with a phenyl ether structure, compositions and use

Thiadiazabicyclononane derivatives of the formula I ##STR1## (R.sup.1 =H, F; R.sup.2 =halogen; R.sup.3 =H, C.sub.1 -C.sub.4 -alkyl; R.sup.4 =H, C.sub.1 -C.sub.8 -alkoxycarbonyl, C.sub.3 -C.sub.6 -alkenyloxycarbonyl or C.sub.3 -C.sub.5 -alkynyloxycarbonyl, and these 3 groups may additionally bear C.sub.1 -C.sub.4 -alkoxy; X, Y, Z=O,= S; a=C.sub.2 -C.sub.3 -alkylene chain which in addition to R.sup.4 may bear up to 3 identical or different radicals R.sup.5 : OH, COOH, C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.6 -alkoxycarbonyl, and the last two radicals may in turn bear up to 5 halogen atoms or one of the following substituents; OH, CN, SH, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.6 -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, C.sub.1 -C.sub.6 -alkylcarbonyloxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkoxycarbonyl-C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.6 -alkoxycarbonyl-C.sub.1 -C.sub.4 -alkylthio). These thiadiazabicyclononane derivatives are suitable for use as herbicides.

Herbicidal thiadiazabicyclononane derivatives

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

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;

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Speyer, Germany

Lothar Rueb