Publication number: 20090048319
Abstract: A method of using a micronutrient selected from the group consisting of salts and adducts of Mg, Ca, B, Mn, Fe, Co and Zn and Mo as a safener for a triazole, selected from the group consisting of azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimenol, triadimefon and triticonazole or salts or adducts thereof for controlling harmful fungi.
Type:
Application
Filed:
February 7, 2007
Publication date:
February 19, 2009
Inventors:
Harald Kohle, Martin P. Mascianica, Albert C. Everson, Thomas J. Holt, Ted R. Berdinelli, Charles W. Finch
Publication number: 20080262000
Abstract: 5-Alkoxyalkyl-6-alkyl-7-aminoazolopyrimidines of the formula I in which the substituents are defined as follows: R1 is alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, cyanoalkyl, and benzyloxyalkyl, where the groups in the aliphatic or aromatic moiety may be unsubstituted or may have substitution by from one to three groups Ra: Ra is halogen, cyano, nitro, hydroxy, cycloalkyl, alkoxy, alkylthio, and NRARB; RA, RB are hydrogen and alkyl; R2 is alkoxyalkyl, phenoxyalkyl, alkylthioalkyl, and phenylthioalkyl, which groups may have no substitution or may have substitution according to the description; R3 is hydrogen and alkyl; A is N and C—RA; processes for preparation of these compounds, compositions comprising them, and their use for controlling phytopathogenic harmful fungi.
Type:
Application
Filed:
February 14, 2006
Publication date:
October 23, 2008
Applicant:
BASF Aktiengesellschaft
Inventors:
Peter Schafer, Udo Hunger, Maria Scherer, Harald Kohle, Helmut Schiffer, Thomas Grote, Jochen Dietz, Wassilios Grammenos, Jan Klaas Lohmann, Bernd Muller, Joachim Rheinheimer, Frank Schieweck, Anja Schwogler
Publication number: 20080039320
Abstract: The use of menadione or one of its plant-compatible acid addition salts for enhancing the activity of agrochemicals against phytopathogenic fungi, mixtures of menadione and at least one active compound selected from the following groups: A) azoles, such as cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, hexaconazole, imazalil, metconazole, myclobutanil, penconazole, prochloraz, prothioconazole, tebuconazole, triadimefon, triadimenol, triflumizole; B) strobilurins, such as azoxystrobin, dimoxystrobin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin or trifloxystrobin; C) acylalanines, such as benalaxyl, metalaxyl, mefenoxam, ofurace, oxadixyl; D) amine derivatives, such as spiroxamine; E) anilinopyrimidines, such as pyrimethanil, mepanipyrim or cyprodinil; F) dicarboximides, such as iprodione, procymidone, vinclozolin; G) cinnamides and analogs, such as dimethomorph, flumetover or flumorph; H) dithiocarbamates, such as ferbam, nabam, mane
Type:
Application
Filed:
November 24, 2005
Publication date:
February 14, 2008
Inventors:
Harald Kohle, Reinhard Stierl, Randall Gold, Felix Gorth, John-Bryan Speakman, Peter Dombo, Martin Semar, Dieter Strobel, Matthias Niedenbruck, Hans Bestman
Publication number: 20080027085
Abstract: 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, whereby: k represents 0, 1, 2, 3; m represents 0, 1, 2, 3, 4 or 5; n represents 1, 2, 3, 4 or 5; R1, independent of one another, represents halogen, OH, CN, NO2, C1-C4 alkyl, C1-C4 alkyl halide, C1-C4 alkoxy, C1-C4 alkoxy halide, C2-C4 alkenyl, C2-C4 alkynyl, C3-C8 cycloalkyl, C1-C4 alkoxy-C1-C4 alkyl, amino, phenoxy, which is optionally substituted by halogen or C1-C4 alkyl, NHR, NR2, C(Ra)?N—ORb, S(?O)pA1 or C(?O)A2, or two radicals R1 bound to adjacent carbon atoms can, together, also represent a group —O-Alk-O—, wherein Alk represents a linear or branched C1-C4 alkylene, and 1, 2, 3 or 4 hydrogen atoms can also be replaced by halogen; R2 represents C1-C4 alkyl halide, C1-C4 alkoxy, C1-C4 alkoxy halide, hydroxy, halogen, CN or NO2; whereby R2 can also represent hydrogen or C1-C4 a
Type:
Application
Filed:
July 22, 2005
Publication date:
January 31, 2008
Applicant:
BASF AKTIENGESELLSCHAFT
Inventors:
Wassilios Grammenos, Thomas Grote, Carsten Blettner, Markus Gewehr, Udo Hunger, Bernd Muller, Joachim Rheinheimer, Peter Schafer, Frank Schieweck, Anja Schwogler, Ulrich Schofl, Harald Kohle, Siegfried Strathmann, Maria Scherer, Reinhard Stierl, Jan Rether
Publication number: 20060172887
Abstract: A method of inducing virus tolerance of plants which comprises treating the plants, the soil or seeds with an effective amount of a compound of the formula I in which X is halogen, alkyl or trifluoromethyl; m is 0 or 1; Q is C(?CH—CH3)—COOCH3, C(?CH—OCH3)—COOCH3, C(?N—OCH3)—CONHCH3, C(?N—OCH3)—COOCH3, N(—OCH3)—COOCH3, or a group Q1 wherein # denotes the bond to the phenyl ring; A is —0—B, —CH2O—B, —OCH2—B, —CH2S—B, —CH?CH—B, —C?C—B, —CH2O—N?C(R1)—B, —CH2S—N?C(R1)—B, —CH2O—N?C(R1)—CH?CH—B, or —CH2O—N?C(R1)—C(R2)?N—R3, where B is phenyl, naphthyl, 5- or 6-membered hetaryl or 5- or 6-membered hetero-cyclyl, containing one to three N atoms and/or one O or S atom or one or two O and/or S atoms, the ring systems being unsubstituted or substituted as defined in the description; R1 is hydrogen, cyano, alkyl, haloalkyl, cycloalkyl, alkoxy, or alkylthio; R2 is phenyl, phenylcarbonyl, phenylsulfonyl, 5- or 6-membered hetaryl, 5- or 6-membered hetarylcarbonyl or 5- or 6-membered hetarylsulfonyl, the ring syste
Type:
Application
Filed:
September 21, 2005
Publication date:
August 3, 2006
Inventors:
Harald Kohle, Uwe Conrath, Kai Sechaus, Matthias Niedenbrock, Marco-Antonio Tavares-Rodrigues, Waldemar Sanchez, Edson Begliomini, Claudio Oliveira