| |
 |
|
|
Inventor: Muller; Bernd
Address: Frankenthal, DE
No. of patents: 119
Patents:
| Patent Number |
Title Of Patent |
Date Issued |
| 7601673 |
Fungicidal mixtures |
October 13, 2009 |
| Fungicidal mixtures, comprising, as active components, 1) a sulfamoyl compound of the formula I, ##STR00001## in which the substituents are as defined below: R.sup.1 is hydrogen, halogen, cyano, alkyl, haloalkyl, alkoxy, alkylthio, alkoxycarbonyl, phenyl, benzyl, formyl or CH.dbd.NOA; |
| 7550471 |
5-alkyl-7-aminotriazolopyrimidines, methods and intermediary product necessary for the productio |
June 23, 2009 |
| 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: R.sup.1 and R.sup.2 each is a hydrogen atom or a group of alkyl, alcenyl, haloalkyl, cycloalky, phenyl or naphtyle, satur |
| 7501530 |
Trifluoromethyl-thiophene carboxylic acid aniledes and use thereof as fungicides |
March 10, 2009 |
| 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 a |
| 7501383 |
Substituted [1,2,4]triazolo[1,5-a]pyrimidines and their use for controlling harmful fungi |
March 10, 2009 |
| The invention relates to 5,6-dialkyl-7-amino-triazolopyrimidines of formula (I), in which the substituents are defined as follows: R.sup.1 represents alkyl or alkoxyalkyl; R.sup.2 represents alkyl, R.sup.1 and/or R.sup.2 being substituted according to the description. The invention a |
| 7488732 |
2-substituted pyrimidines |
February 10, 2009 |
| 2-Substituted pyrimidines of the formula I ##STR00001## in which the index n and the substituents L, R.sup.a, R.sup.b, R.sup.c, R.sup.z, R.sup.u, R.sup.v, A', A'' and A''' are as defined in the description and: R.sup.1 is C.sub.3-C.sub.10-alkyl, C.sub.3-C.sub.10-alkenyl, C.sub.3-C.s |
| 7465735 |
5-Phenypyrimidines their preparation compositions comprising them and their use |
December 16, 2008 |
| 5-Phenylpyrimidines, their preparation, compositions comprising them and their use 5-Phenylpyrimidines of the formula I ##STR00001## in which the substituents and the index are as defined below: R.sup.1,R.sup.2 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, hal |
| 7449471 |
5-phenylpyrimidines, their preparation, compositions comprising them and their use |
November 11, 2008 |
| 5-Phenylpyrimidines of the formula I ##STR00001## in which the substituents and the index are as defined below: R.sup.1,R.sup.2 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, alkynyl or haloalkynyl, and R.sup.1 and R.sup.2 together with the nitroge |
| 7388018 |
4-Piridinylmethylsulphonamide derivatives as fungicidal plant protein agents |
June 17, 2008 |
| Sulfonamides of the formula I ##STR00001## where the substituents are as follows: R.sup.1 is hydrogen, alkyl, alkoxy, alkenyl or alkynyl; and R.sup.2, R.sup.3, R.sup.4, R.sup.5 are hydrogen, halogen, alkyl, alkoxy or halomethyl; R.sup.2 and R.sup.3 together may also form a phenyl, c |
| 7375108 |
2-substituted pyrimidines |
May 20, 2008 |
| The invention relates to 2-substituted pyrimidines of the formula I ##STR00001## in which the index n and the substituents R.sup.1 to R.sup.3 and L are as defined in the description and R.sup.4 corresponds to one of the formulae ##STR00002## in which R.sup.a, X and R.sup.b are as |
| 7368414 |
Fungicidal mixtures |
May 6, 2008 |
| Fungicidal mixtures, comprising A) carbamates of the formula I, ##STR00001## in which X is CH or N, n is 0, 1 or 2 and R is halogen, C.sub.1-C.sub.4-alkyl or C.sub.1-C.sub.4-haloalkyl, where the radicals R can be different if n is 2, one of its salts or adducts and, B) imidazole |
| 7320975 |
2-(2-pyridyl)-5-phenyl-6-aminopyrimidine, method and intermediate products for the production an |
January 22, 2008 |
| The invention relates to 2-(2-pyridyl)-5-phenyl-6-aminopyrimidines of formula I, wherein the substitutes and the index have the following meaning: R.sup.1 represents halogen, hydroxy, hyano, hxo, nitro, amino, mercapto, alkyl, halogenalkyl, alkenyl, alkinyl, cycloalkyl, alkoxy, halog |
| 7317015 |
2-Substituted pyrimidines |
January 8, 2008 |
| The invention relates to 2-substituted pyrimidines of the formula I ##STR00001## in which the index n and these substituents R.sup.1, R.sup.2 and R.sup.3 are as defined in the description and R.sup.4 is as defined below: R.sup.4 corresponds to one of the formulae ##STR00002## whe |
| 7307172 |
7-amino triazolopyrimidines for controlling harmful fungi |
December 11, 2007 |
| The invention relates to 7-amino triazolopyrimidines of formula (I), in which the substituents have the following meanings: R.sup.1, R.sup.2 represent hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, phenyl, naphthyl; or 5-membered or 6-membered heterocyclyl containing one to four nitr |
| 7300908 |
Fungicidal triazolopyrimidines, method for the production thereof and use thereof in controlling |
November 27, 2007 |
| Triazolopyrimidines of formula (I), wherein the index and substituents have the following meaning: n=0 or a whole number of 1-5; R=halogen, cyano, hydroxy, cyanate, alkyl, alkenyl, alkinyl, halogenalkyl, halogenalkenyl, alkoxy, alkenyloxy, alkinyloxy, halogenalkoxy, cycloalkyl, cyclo |
| 7186861 |
Z-substituted acrylamides, methods for production thereof and agents comprising the same |
March 6, 2007 |
| Z-substituted acrylamides of formula (I), where the substituents have the following meanings: X.dbd.H, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, with X in the 3- or 4-position, n=1 or 2, where X can be different if n=2, R.sup.1=alkyl, haloalkyl, cycloalkyl, alkoxy, haloalkoxy, a |
| 7186672 |
Fungicidal mixtures |
March 6, 2007 |
| Fungicidal mixtures comprising a) a benzophenone of the formula I, b) a carbamate of the formula II, and c) an azole derivative of the formula III in a synergistically effective amount, and a method for controlling harmful fungi using mixtures of the compounds I, II and III are descr |
| 7153860 |
5-Phenylpyrimidines, methods and intermediate products for the production thereof and use of the |
December 26, 2006 |
| The invention relates to 5-phenylpyrimidine of formula (I) wherein the substituents have the following designations: R.sup.1 represents a five to ten-membered saturated, partially unsaturated or aromatic monocyclic or bicyclic heterocycle which contains between one and four heteroatoms |
| 7148227 |
Fungicidal triazolopyrimidines, methods for producing the same, use thereof for combating harmfu |
December 12, 2006 |
| The invention relates to triazolopyrimidines of formula (I), in which the substituents are defined as follows: L.sup.1 represents cyano, S(.dbd.O).sub.nA.sup.1 or C(.dbd.O)A.sup.2, wherein A.sup.1 stands for hydrogen, hydroxy, alkyl, alkylamino or dialkylamino; A.sup.2 stands for C.s |
| 7094894 |
Fungicidal triazolopyrimidines, method for the production thereof, use thereof for controlling h |
August 22, 2006 |
| Disclosed are a method for producing fungicidal triazolopyrimidine compounds, agents containing said compounds, and the use thereof for controlling harmful fungi. Also disclosed are triazolopyrimidines of formula (I), in which the substituents have the following meaning: L.sup.1 repr |
| 7071334 |
6-(2-chloro-6-fluoro-phenyl)-triazolopyrimidines |
July 4, 2006 |
| 6-(2-Chloro-6-fluoro-phenyl)-triazolopyrimidines of formula (I), in which R.sup.1 and R.sup.2 independently denote hydrogen or alkyl, alkenyl, alkynyl, alkadienyl, or haloalkyl, cycloalkyl, bicycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four nitro |
| 7056941 |
2-[pyrazolyl and triazolyl-3'-oxymethylene]-phenyl-isoxazolones, triazolones and tetrazolones as |
June 6, 2006 |
| 2-[Pyrazolyl- and triazolyl-3'-oxymethylene]phenylisoxazolones, -triazolones and -tetrazolones of formula I ##STR00001## where: X is a group A, B or C, ##STR00002## where # denotes the bond with the phenyl ring, R.sup.a is hydrogen, halogen, alkyl or alkoxy, R.sup.b is alkyl; |
| 7038047 |
Substituted 6-(2-methoxyphenyl) triazolopyrimides as fungicides |
May 2, 2006 |
| Substituted 6-(2-methoxy-phenyl)-triazolopyrimidines of formula I ##STR00001## in which R.sup.1 and R.sup.2 independently denote hydrogen or alkyl, alkenyl, alkynyl, or alkadienyl, haloalkyl, haloalkenyl, cycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing o |
| 6855718 |
7-(r)-aminotriazolopyrimidines, the production thereof and use of the same for combatting phytop |
February 15, 2005 |
| A 7-(R)-Aminotriazolopyrimidines of formula I ##STR1##where the substituents and index are as defined below: R.sup.1 is hydrogen or methyl; R.sup.2 is methyl; R.sup.3 is C.sub.2 -C.sub.10 -alkyl, C.sub.1 -C.sub.4 -alkoxymethyl, C.sub.3 -C.sub.10 -cycloalkyl; Y is halogen, cyano, |
| 6767923 |
Benzhydryl derivatives |
July 27, 2004 |
| Benzhydryl derivatives of the formula I, ##STR1##where the index and the variables are as defined below: X is oxygen or sulfur; R.sup.1, R.sup.3 are halogen, cyano, nitro, hydroxyl, mercapto, amino, alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, alkylcarbonyloxy, formylox |
| 6730680 |
6-phenyl-pyrazolopyrimidines |
May 4, 2004 |
| 6-Phenyl-Pyrazolopyrimidines of formula I ##STR1##wherein R.sup.1 is alkyl, alkenyl, alkynyl, alkadienyl or haloalkyl, cycloalkyl, bicycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur |
| 6696607 |
Use of phenethyl acrylamides, novel phenethyl acrylamides, method for the production thereof and |
February 24, 2004 |
| Use of phenethylacrylamides of the formula I: ##STR1##in which the substituents have the following meanings: X is halogen, alkyl, haloalkyl, alkoxy, haloalkoxy and --O--C(R.sup.a,R.sup.b)--C.ident.C--R.sup.6 ; R.sup.a,R.sup.b and R.sup.c have the meanings given in the description; m |
| 6693124 |
Bisimino-substituted phenyl compounds and their use as pesticides |
February 17, 2004 |
| Bisimino-substituted phenyl compounds of the formula I ##STR1##where the substituents have the following meanings: X is a group A or B ##STR2## where # denotes the bond with the phenyl ring and R.sup.a is halogen, alkyl or alkoxy; Y is halogen, alkyl, haloalkyl or alkoxy; |
| 6593315 |
Salicylic acid derivatives, processes for their preparation, compositions comprising them, and t |
July 15, 2003 |
| Salicylic acid derivatives of the formula I, ##STR1##where the index and the substituents have the following meanings: X is halogen, NO.sub.2, cyano, alkyl or alkoxy; m is 0, 1, 2 or 3, it being possible for the substituents X to be different from each other if n is greater than 1; |
| 6583090 |
Hetaryl-substituted benzyl phenyl ethers, method for the production thereof, and their use for c |
June 24, 2003 |
| The invention relates to hetaryl-substituted benzyl phenyl ethers of formula (I) in which the substituents have the following meanings: (Q): ##STR1##C(.dbd.CHOCH.sub.3)--COOCH.sub.3, C(.dbd.CHCH.sub.3)--COOCH.sub.3, C(.dbd.NOCH.sub.3)--COOCH.sub.3, C(.dbd.NOCH.sub.3)--CONHCH.sub.3, N |
| 6576595 |
Xanthone derivatives, processes for their preparation and their use for controlling harmful fung |
June 10, 2003 |
| Xanthone derivatives of the formula I ##STR1##where the index and the variables are as defined below: n is 0, 1 or 2; R.sup.1 is alkyl or haloalkyl; R.sup.2,R.sup.3 are alkoxy, alkenyloxy or alkynyloxy, or R.sup.2 and R.sup.3 together form an unsubstituted or substituted oxyalkylene |
| 6562833 |
Use of 2-(n-phenylamino)pyrimidines as fungicides, and novel 2-(n-phenylamino) pyrimidines |
May 13, 2003 |
| 2-(N-phenylamino)pyrimidines of the formula I, ##STR1##where: R.sup.1, R.sup.3 independently of one another are cyano, C.sub.1 -C.sub.8 -alkyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkynyl, where the radicals alkyl, alkenyl and alkynyl may be substituted by cyano, halogen, |
| 6559151 |
6-(2-trifluoromethyl-phenyl)-triazolopyrimidines |
May 6, 2003 |
| 6-(2-Trifluoromethyl-phenyl)-triazolopyrimidines of formula I ##STR1##in which R.sup.1 and R.sup.2 independently denote hydrogen or alkyl, alkenyl, alkynyl, alkadienyl, or haloalkyl, cycloalkyl, bicycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four |
| 6552026 |
6-phenyl-pyrazolopyrimidines |
April 22, 2003 |
| 6-Phenyl-Pyrazolopyrimidines of formula I ##STR1##wherein R.sup.1 is alkyl, alkenyl, alkynyl, alkadienyl or haloalkyl, cycloalkyl, bicycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur |
| 6537989 |
Azadioxacycloalkene derivatives, methods for the production thereof and their use as fungicides |
March 25, 2003 |
| The present invention relates to azadioxacycloalkenes of the formula I ##STR1##in which the substituents R.sup.1 to R.sup.5 and X, the index n and the bridge member W have the following meanings: R.sup.1 is C.sub.1 -C.sub.4 -alkyl, halogen, C.sub.1 -C.sub.4 -haloalkyl, C.sub.3 -C.sub. |
| 6528536 |
Fungicidal mixtures |
March 4, 2003 |
| A fungicidal mixture comprises a.sub.1) a phenyl benzyl ether derivative of the formula I.a, I.b or I.c ##STR1## and/or a.sub.2) a carbamate of the formula Id ##STR2## where X is CH or N, n is 0, 1 or 2 and R is halogen, C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -haloalkyl |
| 6514998 |
2-[1', 2', 4'-triazol-3'-yloxymethlene]anilides, their preparation and their use |
February 4, 2003 |
| 2-[1',2',4'-Triazol-3'-yloxymethylene]anilides of the formula I ##STR1##where the index and the substituents have the following meanings: n is 0, 1, 2, 3 or 4; X is a direct bond, O or NR.sup.a ; R.sup.a is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl; R.sup.1 is nit |
| 6509379 |
Phenylacetic acid derivatives, process and intermediate products for their preparation, and thei |
January 21, 2003 |
| Phenylacetic acid derivatives of the formula I ##STR1##where the variables are as disclosed herein, their salts, processes and intermediates for their preparation, and their use for controlling harmful fungi and animal pests. |
| 6503936 |
Fungicidal mixtures |
January 7, 2003 |
| A fungicidal mixture comprising a.1) a carbamate of the formula I.a, ##STR1## in which X is CH or N, n is 0, 1 or 2 and R is halogen, C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -haloalkyl, where the radicals R can be different if n is 2, and b) a copper-containing fungicidal a |
| 6489360 |
Fungicidal mixtures |
December 3, 2002 |
| A fungicidal mixture comprises a.sub.1) a phenyl benzyl ether derivative of the formula I.a, I.b or I.c ##STR1## and/or a.sub.2) a carbamate of the formula Id ##STR2## where X is CH or N, n is 0, 1 or 2 and R is halogen, C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -haloalky |
| 6482984 |
Iminooxy-substituted benzyl phenyl ethers, processes and intermediates for their preparation, co |
November 19, 2002 |
| Iminooxy-substituted benzyl phenyl ethers of the formula I ##STR1##in which the substituents and the index are as defined below: Y is H, CH.sub.3, F or Cl; Q is C(.dbd.CHOCH.sub.3)--COOCH.sub.3, C(.dbd.CHCH.sub.3)--COOCH.sub.3, C(.dbd.NOCH.sub.3)--COOCH.sub.3, C(.dbd.NOCH.sub.3)--CONHC |
| 6469195 |
2-phenoxyphenylacetic acid derivatives, method and intermediate products for the production ther |
October 22, 2002 |
| 2-Phenoxyphenylacetic acid derivatives of the formula I ##STR1##where the substituents and the index have the following meanings: A is ##STR2## where R.sub.1 is halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, CF.sub.3, C.sub.1 -C.sub.4 -haloalkoxy, formyl, C(.dbd.O)NR.s |
| 6455515 |
Salicylohydrazide derivatives, processes and intermediates for their preparation, compositions c |
September 24, 2002 |
| Salicylohydrazide derivatives of the formula I ##STR1##in which the index and the substituents have the following meanings: X is halogen, NO.sub.2, cyano, alkyl or alkoxy; m is 0, 1, 2 or 3, it being possible for the substituents X to differ from each other if n is greater than 1; R |
| 6451790 |
Azadioxacycloalkenes and their use for combating harmful fungi and animal pests |
September 17, 2002 |
| Compounds of formula I ##STR1##wherein W is optionally substituted alkylene; Y is N or CR.sup.a ; R.sup.a is hydrogen, halogen or alkyl; R.sup.1.sub.n represents hydrogen or 1 to 4 substituents; R.sup.2 is hydrogen, nitro, cyano, halogen, alkyl, haloalkyl, alkoxy, alkylthio or |
| 6444692 |
Fungicidal mixtures |
September 3, 2002 |
| A fungicidal mixture, comprising at least one compound selected from a) carbamates of the formula I, ##STR1## where T is CH or N, n is 0, 1 or 2 and R is halogen, C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -haloalkyl, it being possible for the radicals R to be different if n is 2 |
| 6423733 |
Fungicidal mixtures |
July 23, 2002 |
| A fungicidal mixture comprises a) a phenyl benzyl ether derivative of the formula I.a, I.b or I.c, ##STR1## and/or a carbamate of the formula Id ##STR2## where X is CH or N, n is 0, 1 or 2 and R is halogen, C.sub.l -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -haloalkyl, it being possib |
| 6414031 |
Bisoximether derivatives, methods and intermediate products for the production thereof, and thei |
July 2, 2002 |
| There are disclosed bisoxime ether derivatives of the formula I ##STR1##in which the variables have the following meanings:R.sup.1 is halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy or C.sub.1 -C.sub.4 -haloalkoxy;n is 1 to 5, it being possible for the |
| 6380231 |
Azolyloxybenzylalkoxyacrylic esters, their preparation and their use |
April 30, 2002 |
| Compounds of formula I ##STR1##whereinn is 0, 1, 2, 3, or 4;R is nitro, cyano, halogen, unsubstituted or substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy or two adjacent radicals R form an optionally substituted three or four membered bridge;R.sup.1, R.sup.2 are C.sub. |
| 6372766 |
Substituted 2-(2'-pyridyloxy)phenylacetamides, as fungicides and pesticides |
April 16, 2002 |
| Substituted 2-(2'-pyridyloxy)phenylacetamides I, ##STR1##whereR.sup.1 is fluorine, chlorine, CH.sub.3 or halomethyl;R.sup.2 is fluorine, bromine, alkyl or halomethyl;R.sup.3 is hydrogen or one of the radicals mentioned under R.sup.2 ; andR.sup.2 is 6-chloro if R.sup.3 is hydrogen,R.sup.3 is 5-ch |
| 6369090 |
Fungicidal mixture |
April 9, 2002 |
| Fungicidal mixtures comprisea.1) a carbamate of the formula I.a, ##STR1## in which X is CH or N, n is 0, 1 or 2 and R is halogen, alkyl or haloalkyl, ora.2) the oxime ether carboxamide of the formula I.b ##STR2## andb.1) 4-[2-methyl-3-(4-tert-butylphenyl)propyl]-2,6-dimethyl morpholine |
| 6365614 |
Fungicides mixtures |
April 2, 2002 |
| A fungicidal mixture, comprising at least one active compound selected froma.sub.1) carbamates of the formula Ia, ##STR1## where T is CH or N, n is 0, 1 or 2 and R is halogen, C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -haloalkyl, it being possible for the radicals R to be different if |
|
|
|
