Basf Aktiengesellschaft

Basf Se Corporation

Abbott Gmbh & Co Kg

Other

Joachim Rheinheimer

Ernst Baumann

Thomas Grote

Karl-Otto Westphalen

Siegfried Strathmann

Wassilios Grammenos

Helmut Walter

Markus Gewehr

Eberhard Ammermann

Uwe Josef Vogelbacher

Frank Schieweck

Gisela Lorenz

Reinhard Stierl

Jordi Tormo I Blasco

Peter Schäfer

Andreas Gypser

Bernd Müller

Michael Rack

Wolfgang Von Deyn

Matthias Witschel

Karl Eicken

Ingo Rose

Ulf Misslitz

Regina Luise Hill

Anja Schwögler

Martina Otten

Guido Mayer

Stefan Engel

Uwe Kardorff

Oliver Wagner

Carsten Blettner

Matthias Gerber

Hubert Sauter

Liliane Unger

Joachim Gebhardt

Wolfgang Wernet

Manfred Raschack

Hartmut Riechers

Dagmar Klinge

Ulrich Schöfl

Andreas Kling

Wilhelm Amberg

Norbert Götz

Maria Scherer

Stefan Muller

Bruno Wuerzer

Peter Sch&auml;fer

Michael Keil

Bernd W M&uuml;ller

Norbert Meyer

Helmut Hagen

Wilhelm Rademacher

Rene Lochtman

John-Bryan Speakman

Jan Klaas Lohmann

Matthias Bratz

Jochen Dietz

Frank Wetterich

Gerhard Hamprecht

Albrecht Harreus

Christian Harald Winter

Franz Roehl

Ana Escribano Cuesta

Thomas Saupe

Peter Plath

Hans Theobald

Egon Haden

Hartmann Konig

Jurith Montag

Heinz Isak

Oliver Cullmann

Gerhard Paul

Jens Renner

Norbert Goetz

Thomas Zierke

Thomas Kuekenhoehner

Volker Maywald

Michael Puhl

Norbert G&ouml;tz

Norbert Gotz

Klaus Grossmann

Tobias Mentzel

Ansgar Gereon Altenhoff

Christine Wiebe

Sebastian Peer Smidt

Joachim Schmidt-Leithoff

Wolfgang Rohr

Johann Jung

Bernd Mueller

Klaus Ditrich

Ian Robert Craig

Claus Bollschweiler

Peter Schaefer

Ronan Le Vezouet

Marcus Fehr

Barbara Nave

Harald Köhle

Juergen Frank

Siegfried Bialojan

Martin Sukopp

The present invention relates to the use of novel oxadiazoles of the formula I or an N-oxide and/or their agriculturally useful salts for controlling phytopathogenic fungi, or to a method for combating phytopathogenic harmful fungi, which process comprises treating the fungi or the materials, plants, the soil or seeds to be protected against fungal attack, with an effective amount of at least one compound of formula I or an N-oxide or an agriculturally acceptable salt thereof; and to agrochemical compositions comprising at least one such compound and to agrochemical compositions further comprising seeds. 

Use of substituted oxadiazoles for combating phytopathogenic fungi

The present invention relates to a process for preparation of intermediates (Z,2E)-5-hydroxy-2-methoxyimino-N-methyl-pent-3-enamides from 4-substituted 5-meth-oxyimino-2H-pyran-6-ones and their processing for example to (Z)-5-cyclyloxy-2-[(E)-methoxyimino]-3-methyl-pent-3-enic acid methyl amides. The invention also relates to a process for preparation of 4-substituted 5-imino-2H-pyran-6-ones and to novel intermediates for the preparation of fungicidal (Z)-5-cyclyloxy-2-[(E)-methoxyimino]-3-methyl-pent-3-enic acid methyl amides.

Stereoselective process to obtain (Z)-5-cyclyloxy-2-[(E)-methoxyimino]-3-methyl-pent-3-enic acid methyl amides using E,Z-isomer mixture of and intermediates thereof

The present invention relates to the use of strobilurine type compounds of formula I and the N-oxides and the salts thereof for combating phytopathogenic fungi containing a mutation in the mitochondrial cytochrome b gene conferring resistance to Qo inhibitors, and to methods for combating such fungi. The invention also relates to novel compounds, processes for preparing these compounds, to compositions comprising at least one such compound, to plant health applications, and to seeds coated with at least one such compound.

Use of strobilurin type compounds for combating phytopathogenic fungi resistant to Qo inhibitors

The present invention relates to fungicidal mixtures, comprising at least one fungicidally active strobilurin-type compound I and at least one fungicidally active compound or biopesticide II as defined in the description, and to compositions comprising these mixtures.

Fungicidal mixtures I comprising strobilurin-type fungicides

5,6-Dialkyl-7-aminotriazolopyrimidines of the formula I in which the substituents are as defined below:

5,6-Dialkyl-7-aminotriazolopyrimidines, their preparation and their use for controlling harmful fungi, and compositions comprising these compounds

Use of strobilurin type compounds for combating phytopathogenic fungi resistant to QO inhibitors

Benzoyl derivatives of the formula I where the variables have the following meanings:

3-heterocyclyl-substituted benzoyl derivatives

Process for the preparation of aromatic and heteroaromatic carboxylic acids, carboxylic acid esters and carboxamides by the reaction of aromatic or heteroaromatic halides R&#x2014;X, in which n=integer from 1 to 6, R=substituted or unsubstituted and aromatic or heteroaromatic radical and X=chlorine, bromine or iodine atom, with carbon monoxide and water, ammonia, alcohols or amines in the presence of bases and zero-valent or divalent palladium compounds and bidentate diphosphanes or complexes of zero-valent or divalent palladium with bidentate diphosphanes, in which use is made of bidentate diphosphanes(R&#x2014;)(R&#x2014;)P&#x2014;Y&#x2014;P(&#x2014;R)(&#x2014;R)in which Rto R=unsubstituted aryl radicals or aryl radicals substituted with at least one radical exhibiting a positive resonance effect or a positive inductive effect, or unsubstituted or substituted cycloalkyl radicals, and Y=hydrocarbon group with a total of 2 to 20 carbon atoms, in which at least one of the carbon atoms carries only one or no hydrogen atom as substituent; except for the reaction of 4-bromo-3-difluoromethyl-1-methylpyrazole with 2-(3,4,5-trifluorophenyl)aniline and carbon monoxide to give N-[2-(3,4,5-trifluorophenyl)phenyl]-3-difluoromethyl-1-methylpyrazole-4-carboxamide.

Method for producing aromatic and heteroaromatic carboxylic acids, carboxylic acid esters and carboxylic acid amides

Compounds of the formula I in which the substituents have the meaning given in the description, processes for preparing these compounds, compositions comprising them and their use for controlling harmful fungi.

Fungicidal compounds, method for the production thereof, and use thereof to combat damaging fungi, and agents comprising the same

Carboxylic acid derivatives where R&#x2014;R, X, Y and Z have the meanings stated in the description, and the preparation thereof, are described. The novel compounds are suitable for controlling diseases.

Carboxylic acid derivatives, their preparation and use

The present invention relates to novel pyridylmethyl-sulfonamide compounds of formula (I) where: n is 0 to 4; m is 0 to 4; Ris halogen, CN, NO, OH, SH, C-C-alkyl, C-C-haloalkyl, C-C-alkoxy, C-C-haloalkoxy, etc.; and/or two radicals Rtogether form a fused ring; Ris H, C-C-alkyl, C-C-haloalkyl, C-C-alkenyl, C-C-alkynyl, C-C-cycloalkyl, C-C-alkyl-C-C-cycloalkyl or benzyl; Ris halogen, CN, NO, C-C-alkyl, C-C-haloalkyl, C-C-alkoxy or C-C-haloalkoxy; Y is &#x2014;O&#x2014;, C-C-alkanediyl, &#x2014;O&#x2014;CH&#x2014;, &#x2014;CH&#x2014;O&#x2014;, &#x2014;C(NOR)&#x2014;, &#x2014;S&#x2014;, &#x2014;S(&#x2550;O)&#x2014;, &#x2014;S(&#x2550;O)&#x2014; or &#x2014;N(R)&#x2014;;and the N-oxides, and salts thereof and their use for combating phytopathogenic harmful fungi, and also to compositions and seed comprising at least one such compound.

Pyridylmethyl-sulfonamide compounds

The present invention relates to novel pyrimidylmethyl-sulfonamide compounds and to their N-oxides, their agriculturally acceptable salts and their veterinarily acceptable salts and also to agricultural compositions comprising at least one such compound as active component, and also to their use for controlling harmful fungi. The present invention also relates to a method for controlling arthropod pests.

Pyrimidylmethyl-sulfonamide compounds

The present invention relates to a process for preparing N-substituted (3-dihalomethylpyrazol-4-yl)carboxamides of the formula (I) in which Ris optionally substituted phenyl or C-C-cycloalkyl, Ris hydrogen or fluorine, or Rtogether with Ris optionally substituted C-C-alkanediyl or C-C-cycloalkanediyl, Ris C-C-alkyl, C-C-alkenyl, C-C-alkynyl or C-C-alkoxy-C-C-alkyl, X is F or Cl and n is 0, 1, 2 or 3; which comprisesA) providing a compound of the formula (II) in which X is F or Cl, Y is Cl or Br and Rhas one of the meanings given above andB) reacting a compound of the formula (II) with carbon monoxide and a compound of the formula (III) in which R, Rand n have one of the meanings given above; in the presence of a palladium catalyst;to intermediates used for the preparation according to the process according to the invention, and also to processes for their preparation.

Method for the production of N-substituted (3-dihalomethyl-1-methylpyrazol-4-yl) carboxamides

A process is described for preparing isoxazoles of the formula I where the substituents are as defined below: where R1, R3, R4 and R5 are as defined above, followed by halogenation, thiomethylation, oxidation and acylation to give compounds of the formula I. Also novel intermediates for preparing the compounds of the formula I and novel processes for preparing the intermediates are described.

Preparation of isoxazolin-3-ylacylbenzenes

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Ludwigshafen, Germany

Joachim Rheinheimer