Basf Aktiengesellschaft

Basf Se Corporation

Kanesho Soil Treatment Bvba

Ulrich Schöfl

Reinhard Stierl

Siegfried Strathmann

Thomas Grote

Markus Gewehr

Bernd Müller

Wassilios Grammenos

Joachim Rheinheimer

Maria Scherer

Jordi Tormo I Blasco

Frank Schieweck

Anja Schwögler

Carsten Blettner

Peter Schäfer

Eberhard Ammermann

Andreas Gypser

Oliver Wagner

Klaus Schelberger

Gisela Lorenz

Michael Henningsen

Udo Hünger

Randall Even Gold

Thomas Christen

Matthias Niedenbrück

Jan Rether

Michael Rack

Norbert Götz

John-Bryan Speakman

Harald Köhle

Martin Semar

Miguel Octavio Suarez-Cervieri

John Bedford

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

The invention relates to a fungicidal mixture comprising prothioconazole or a salt or adduct thereof with an inorganic acid an organic acid or a metal ion; and at least one further fungicidal compound, selected from the group consisting of thiram, fenoxanil, benthivalicarb, metalaxyl, fludioxonil and prochloraz, in a synergistically effective amount and to methods for controlling harmful fungi, comprising applying the fungicidal mixture.

Fungicidal mixtures

The invention relates to 2-substituted pyrimidines of the formula I in which the index n and the substituents L and Rto Rare as defined in the description andX is a group &#x2014;CH&#x2014;R, &#x2014;N&#x2014;R&#x2014;, &#x2014;O&#x2014; or &#x2014;S&#x2014;;

2-substituted pyrimidines and their use as pesticides

The invention relates to 2-(pyridin-2-yl)-pyrimidine compounds of general formula (I) and their use for controlling pathogenic fungi and as plant protection products that, as an active constituent, contain compounds of this type: In general formula (I), k represents 0, 1, 2, 3; m represents 0, 1, 2, 3, 4 or 5; n represents 1, 2, 3, 4 or 5; R, independent of one another, represents halogen, OH, CN, NO, C-Calkyl, C-Calkyl halide, C-Calkoxy, C-Calkoxy halide, C-Calkenyl, C-Calkynyl, C-Ccycloalkyl, C-Calkoxy-C-Calkyl, amino, phenoxy, which is optionally substituted by halogen or C-Calkyl, NHR, NR, C(R)&#x2550;N&#x2014;OR, S(&#x2550;O)Aor C(&#x2550;O)A, or two radicals Rbound to adjacent carbon atoms can, together, also represent a group &#x2014;O-Alk-O&#x2014;, wherein Alk represents a linear or branched C-Calkylene, and 1, 2, 3 or 4 hydrogen atoms can also be replaced by halogen; Rrepresents C-Calkyl halide, C-Calkoxy, C-Calkoxy halide, hydroxy, halogen, CN or NO; whereby Rcan also represent hydrogen or C-Calkyl when at least one of the three following conditions is fulfilled: n represents 3, 4 or 5; k represents 1, 2 or 3; if m is not equal to 0, at least one of the radicals Rrepresents a radical that differs from halogen, C-Calkyl, C-Calkoxy and C-Calkyl halide, and; Rrepresents C-Calkyl.

2-(pyridin-2-yl)-pyrimidines and their use for controlling harmful fungi

Substituted 6-(2-halogenphenyl)-triazolopyrimidines of formula I in which

Substituted 6-(2-halogennphenyl)-triazolopyrimidines

The invention relates to 2-substituted pyridines of the formula I in which the index n and the substituents Rto Rand L are as defined in the description and is five- or six-membered hetaryl comprising 1 to 3 heteroatoms selected from the group consisting of O, N and S or is phenyl,and to processes for their preparation, intermediates for their preparation, pesticidal compositions and methods for controlling harmful fungi and animal pests using the compounds according to the invention.

2-substituted pyridines, processes for their preparation and their use for controlling harmful fungi

The invention relates to a fungicidal mixture that comprises (1) 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazolo-3-thion (prothioconazole) or the salts or adducts thereof and at least one further fungicidal composition, selected from (2) boscalid or (3) carboxine or (4) metrafenone or (5) a compound of formula (V) or (6) a compound of formula (VI) or (7) quinoxyfen or (8) dithianon or (9) thiram or (10) mepiquat chlorides or (11) cyazofamid or (12) fenoxanil or (13) a compound of formula (XIII) or (14) thiophanate methyl or (15) carbendazim or (16) metalaxyl or (17) fludioxonil or (18) thiabendazole or (19) quintozene or (20) prochloraz or (21) anthraquinone in a synergistically effective amount. 

Fungicidal mixtures, comprising, as active components, 

The invention relates to 5-alkyl-7-aminotriazolopyrimidines of the formula (I) and to the salts thereof. In said formula substituents have the following meanings: Rand Reach is a hydrogen atom or a group of alkyl, alcenyl, haloalkyl, cycloalky, phenyl or naphtyle, saturated, unstaturated or aromatic heterocycle having from five to six members which contain from one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or Rand Rcan from together with a connecting them nitrogen atom a cycle of 5 to 6 members containing from one to four nitrogen atoms or from one to three nitrogen atoms and one sulfur or oxygen atom, Ris a cycloalkyl or bicycloalkyl group, R, Rand Rcan be substituted in conformity with a description, and X is an alkyl or alkyl halide group. The inventive methods and intermediary products necessary for producing said compounds, agents containing them and the use therefore for fighting against harmful mushroom are also disclosed. 

5-alkyl-7-aminotriazolopyrimidines, methods and intermediary product necessary for the production thereof, agents containing said compounds and the use thereof for fighting against harmful mushrooms

The invention relates to 5,6-dialkyl-7-amino-triazolopyrimidines of formula (I), in which the substituents are defined as follows: Rrepresents alkyl or alkoxyalkyl; Rrepresents alkyl, Rand/or Rbeing substituted according to the description. The invention also relates to a method for producing said compounds, to agents containing the latter and to their use for controlling plant-pathogenic fungi. 

Substituted [1,2,4]triazolo[1,5-a]pyrimidines and their use for controlling harmful fungi

The invention relates to novel biphenyl carboxamides of formula (I), wherein A, R, Z, X, Y, m and n have the meanings given in the description, to multiple methods for producing these substances, to their use for combating unwanted micro-organisms and to novel intermediate products and the production thereof.

Trifluoromethyl-thiophene carboxylic acid aniledes and use thereof as fungicides

2-Substituted pyrimidines of the formula I in which the index n and the substituents L, R, R, R, R, R, R, A', A&#x2033; and A&#x2032;&#x2033; are as defined in the description and:

2-substituted pyrimidines

Sulfonamides of the formula I where the substituents are as follows: Processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.

4-Piridinylmethylsulphonamide derivatives as fungicidal plant protein agents

The invention relates to 2-substituted pyrimidines of the formula I in which the index n and the substituents Rto Rand L are as defined in the description and 

Growing community of inventors

Brühl, Germany

Ulrich Schöfl