Bayer Cropscience Ag

Aventis Cropscience Gmbh

Bayer Intellectual Property Gmbh

Bayer Cropscience Gmbh

Bayer Aktiengesellschaft

Andreas Van Almsick

Christopher Hugh Rosinger

Lothar Willms

Thomas Auler

Hermann Bieringer

Elmar Gatzweiler

Hartmut Ahrens

Dieter Feucht

Erwin Hacker

Monika H Schmitt

Ines Heinemann

Hubert Menne

Thomas Seitz

Stefan Lehr

Heinz Kehne

Martin Jeffrey Hills

Jan Dittgen

Ralf Braun

Isolde Häuser-Hahn

Frank Ziemer

Hans Philipp Huff

Arnim Köhn

Simon Dörner-Rieping

Hansjörg Dietrich

Chieko Ueno

Hansjoerg Dietrich

Guido Bojack

Yoshitaka Sato

Koichi Araki

Teruyuki Ichihara

Shinichi Narabu

Klaus Bernhard Haaf

Elisabeth Asmus

Kei Domon

Shinichi Shirakura

Jean-Claude Millet

Seiji Ukawa

Keiji Endo

Simon Dorner-Rieping

Arnim Kohn

Mark Wilhelm Drewes

Christian Waldraff

Britta Olenik

Anu Bheemaiah Machettira

Arnim Koehn

Fabien Poree

Isolde Haeuser-Hahn

Bernd Laber

Martin Adamczewski

Klaus Trabold

Stephen David Lindell

Simon Doerner-Rieping

Joerg Tiebes

Frank Sixl

Jörg Tiebes

Smita Patel

Hans-Joachim Zeiss

Gerhard Thielking

Rudiger Hain

Rüdiger Hain

Armin Koehn

Isolde Häeuser-Hanh

Marin-Holger Hinz

Sylvia Dworacek

Arnim K&ouml;hn

Katherine Rose Law

Christopher Rosinger

Isolde Hauser-Hahn

Herbicidally active 3-phenylisoxazoline-5-carboxamides of cyclopentenylcarboxylic acid derivatives The invention relates to 3-phenylisoxazoline-5-carboxamides of cyclopentenylcarboxylic acid derivatives of the general formula (I) and their agrochemically acceptable salts and to their use in the crop protection sector.

Herbicidally active 3-phenylisoxazoline-5-carboxamides of cyclopentenylcarboxylic acid derivatives

Compounds having herbicidal activity effective against economically important harmful plants are disclosed. The disclosed compounds exhibit herbicidal activity even at relatively low application rates, while at the same time may exhibit compatibility with crop plants. The disclosed compounds may further be effective and efficient against a large number of weeds and against a broad spectrum of weed grasses. As disclosed herein, 3-phenylisoxazoline-5-carboxamides of S-containing cyclopentenylcarboxylic esters of formula (I) and their salts exhibit herbicidal activity against a broad spectrum of economically important mono- and dicotyledonous annual harmful plants.

Herbicidally active 3-phenylisoxazoline-5-carboxamides of s-containing cyclopentenylcarboxylic esters

Acylated N-(1,2,5-oxadiazol-3-yl)-, N-(1,3,4-oxadiazol-2-yl)-, N-(tetrazol-5-yl)- and N-(triazol-5-yl)arylcarboxamides of the formula (I) and the use thereof as herbicides are described.  In this formula (I), R, V, X, Y and Z are radicals such as hydrogen, organic radicals such as alkyl, and other radicals such as halogen. Q is an oxadiazole, triazole or tetrazole radical. W is CY or N.

Acylated N-(1 ,2,5-oxadiazol-3-yl)-, N-(1,3,4-oxadiazol-2-yl)-, N-(tetrazol-5-yl)- and N-(triazol-5-yl)-aryl carboxamides, and use thereof as herbicides

Herbicide-safener compositions are described, comprising active herbicidal ingredients from the group of the N-(tetrazol-5-yl)- and N-(triazol-5-yl)arylcarboxamides and safeners. These herbicide-safener compositions are particularly suitable for use against harmful plants in crops of useful plants.

Herbicide/safener compositions containing N-(tetrazol-5-yl) aryl carboxylic acid amides and N-(triazol-5-yl) aryl carboxylic acid amides

Herbicide-safener compositions are described, comprising active ingredients from the group of the N-(1,2,5-oxadiazol-3-yl)benzamides and safeners. These herbicidal compositions are particularly suitable for use against harmful plants in crops of useful plants.

Herbicide safener compositions

5-phenyl-substituted N-(tetrazol-5-yl)- and N-(triazol-5-yl)arylcarboxamides of the general formula (I) are described as herbicides.  In this formula (I), W, X, Y, Z and R are radicals such as hydrogen, organic radicals such as alkyl, and other radicals such as halogen. A and B are N and CY.

5-phenyl-substituted N-(tetrazol-5-yl) aryl carboxylic acid amides and N-(triazol-5-yl) aryl carboxylic acid amides, and use thereof as herbicides

A description is given of N-(1,2,5-oxadiazol-3-yl)pyridinecarboxamides of the general formula (I) as herbicides. R in this formula (I) stands for radicals such as hydrogen, organic radicals, and other radicals such as halogen. W stands for a substituted pyridyl radical. 

N-(1,2,5-oxadiazol-3-yl)pyridinecarboxamides and use thereof as herbicides

What is described are oxime ether-substituted benzoylamides of the general formula (I) as herbicides.  In this formula (I), R, Y and Y are radicals such as hydrogen, organic radicals such as alkyl, and other radicals such as halogen. Q is a tetrazolyl, triazolyl or oxadiazolyl radical.

Herbicidally active oxime-ether-substituted benzoylamides

Triazolylpyridine ketones expressed by the following formula (1) and use thereof as herbicides. 

Herbicide triazolylpyridine ketones

N-(Tetrazol-5-yl)- and N-(triazol-5-yl)arylcarboxamides and use thereof as herbicides N-(Tetrazol-5-yl)- and N-(triazol-5-yl)arylcarboxamides of the general formula (I) are described as herbicides.  In this formula (I), X, Y, Z and R represent radicals such as hydrogen, organic radicals such as alkyl, and other radicals such as halogen. A and B represent N and CY.

N-(tetrazol-5-yl)- and N-(triazol-5-yl)arylcarboxamides and use thereof as herbicides

What is described is a thermodynamically stable crystal modification of the herbidically active compound 2-({2-chloro-4-(methylsulfonyl)-3-[(2,2,2-trifluoroethoxy)methyl]phenyl}carbonyl)cyclohexan-1,3-dione (tembotrione). This thermodynamically stable crystal modification has particular advantages in the stability of suspension formulations.

Thermodynamically stable crystal modification of 2-({2-chloro-4-(methylsulfonyl)-3-[(2,2,2-trifluoroethoxy)methyl]phenyl} carbonyl)cyclohexane-1,3-dione

Triazolylpyridine ketones expressed by the following formula (I) and use thereof as herbicides.

A description is given of (4-trifluoromethyl-3-thiobenzoyl)cyclohexanediones of the formula (I) and of their use as herbicides.  In this formula (I), X, R, R, R, and Rare radicals such as hydrogen and organic radicals such as alkyl. A and Z are oxygen or alkylene.

(4-trifluoromethyl-3-thiobenzoyl)cyclohexanediones and use thereof as herbicides

What is described are 3-aminocarbonyl-substituted benzoylcyclohexanediones of the formula (I) as herbicides. In this formula (I), Rto Rare radicals such as hydrogen, organic radicals such as alkyl, and other radicals such as halogen. X is alkylene.

3-aminocarbonyl-substituted benzoylcyclohexanediones and their use as herbicides

What is described are 4-(3-aminobenzoyl)-1,3-dimethylpyrazoles of the general formula (I) and their use as herbicides. In this general formula (I), Rand Rare radicals such as hydrogen and organic radicals, such as alkyl, alkenyl and alkynyl. Y is hydrogen or a protective group, such as tosyl.

4-(3-aminobenzoyl)-1,3-dimethylpyrazoles and their use as herbicides

Growing community of inventors

Karben, Germany

Andreas Van Almsick