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Browse by: INVENTOR PATENT HOLDER PATENT NUMBER DATE
 
 
Inventor:
Vogelbacher; Uwe Josef
Address:
Ludwigshafen, DE
No. of patents:
19
Patents:




Patent Number Title Of Patent Date Issued
7601730 Carboxylic acid derivatives, their preparation and use October 13, 2009
Carboxylic acid derivatives ##STR00001## where R--R.sup.6, 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.
7582647 Carboxylic acid derivatives, their preparation and use September 1, 2009
Carboxylic acid derivatives ##STR00001## where R--R.sup.6, 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.
7253323 Method for the production of benzophenones August 7, 2007
A process for preparing benzophenones of the formula I, ##STR00001## where X may be chlorine, hydroxyl, methoxy or C.sub.1-C.sub.6-alkylcarbonyloxy, and Y may be chlorine or bromine, by reacting an acid chloride of the formula II ##STR00002## where X and Y are as defined above with
7119097 Carboxylic acid derivatives, their preparation and their use October 10, 2006
A compound of the formula ##STR00001## pharmaceutically acceptable salts and enantiomers thereof and pharmaceutical compositions containing this compound, its pharmaceutically acceptable salts and enantiomers are claimed.
7109205 Carboxylic acid derivatives, their preparation and use September 19, 2006
Carboxylic acid derivatives ##STR00001## where R R.sup.6, 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.
6600043 Carboxylic acid derivatives, their preparation and use July 29, 2003
Carboxylic acid derivatives ##STR1##where R-R.sup.6, 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.
6559336 Process for the preparation of 5- and/or 6-substituted-2-hydroxybenzoic acid esters May 6, 2003
There is provided a single-step process for the preparation of a compound of formula I. ##STR1##Compounds of formula I are useful as starting materials in the synthesis of natural products and in the manufacture of benzophenone fungicidal agents.
6255489 Method for producing (hetero)aromatic hydroxylamines July 3, 2001
The invention relates to a method for producing N-acylated (hetero)aromatic hydroxylamine derivatives of formula (I), wherein the substituents, the ring atom and the index have the meanings give in the Description, by hydrogenating a (hetero)aromatic nitro-compound of general formula (II
6133451 Method for producing 2-(3-pyrazolyl-oxymethylene) nitrobenzenes October 17, 2000
2-(3-Pyrazolyloxymethylene)nitrobenzene [sic] derivatives of the formula I ##STR1## where the substituents and indices have the meanings given in the description,are prepared by bromination of an o-nitrotoluene of the formula II ##STR2## and subsequent reaction with a 3-hydroxypy
6040458 Method for producing N-substituted 3-hydroxypyrazoles March 21, 2000
A process is described for preparing N-substituted 3-hydroxypyrazoles of the formula I ##STR1## where R.sup.1 is unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl, aryl or heteroaryl andR.sup.2, R.sup.3 are hydrogen, cyano, halogen and unsubstituted or substituted
5969134 Carboxylic acid derivatives, their preparation and use October 19, 1999
Carboxylic acid derivatives ##STR1## where R-R.sup.6, 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.
5932730 Carboxylic acid derivatives, their preparation and use August 3, 1999
Carboxylic acid derivatives ##STR1## where R-R.sup.6, 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.
5840722 Use of carboxylic acid derivatives as drugs November 24, 1998
A method of inhibiting endothelin receptors by administering to a patient a compound of the formula I ##STR1##
5783521 Substituted pyridylsalicylaldehyde or -salicylic acid derivatives, their preparation and their u July 21, 1998
Substituted pyridylsalicylaldehyde and --salicylic acid derivatives of the formula I ##STR1## where R is a formyl group, a CO.sub.2 H group or a radical which can be hydrolyzed to CO.sub.2 H and the other substituents have the following meanings:R.sup.2 is halogen, alkyl, haloalk
5777118 Process of making 2-salicyl(thio0r oxo) pyrimidine July 7, 1998
Cyclic acetals of the formula I ##STR1## where the substituents have the following meanings: R.sup.1 and R.sup.2 are hydrogen, unsubstituted or substituted alkyl or phenyl; additionally R.sup.1 and R.sup.2 together are an unsubstituted or substituted C.sub.2 -C.sub.6 -alkylene ch
5753594 3-halo-3-hetarylcarboxylic acid derivatives, and processes and intermediates for their preparati May 19, 1998
3-Halo-3-hetarylcarboxylic acid derivatives having the formula I ##STR1## in which R is a formyl group, a group CO.sub.2 H or a radical which can be hydrolyzed to COOH, and the remaining substituents have the following meanings:R.sup.2 and R.sup.3 are halogen, C.sub.1 -C.sub.4 -alkyl
5750469 Subtituted lactic acid derivatives having an N-organic radical in the .beta . May 12, 1998
Substituted lactic acid derivatives having an N-organic radical in the .beta.-position, of the formula I ##STR1## where substituents R to R.sup.5, X and Y have the meanings mentioned in the description and N is one of the radicals:a) --N.sub.3, --NC, --NCS or --NCOb) ##STR2##
5703017 3-(Het) arylcarboxylic acid derivatives, their preparation and intermediates for their preparati December 30, 1997
3-(Het)arylcarboxylic acid derivatives of the formula I ##STR1## where R is formyl, CO.sub.2 H or a radical hydrolyzable to COOH and the other substituents have the following meanings:R.sup.2 and R.sup.3 are each halogen, alkyl, haloalkyl, alkoxy, haloalkoxy or alkylthio;X is nitroge
5661106 3-(Het)aryloxy(thio)carboxylic acid derivatives, their preparation and intermediates for their p August 26, 1997
3-(Het)aryloxy(thio)carboxylic acid derivatives of the formula I ##STR1## where R.sup.1 is hydrogen, COOH or a radical which can be hydrolyzed to give COOH;R.sup.2 and R.sup.3 are each halogen, alkyl, haloalkyl, alkoxy, haloalkoxy or alkylthio;X is nitrogen or CR.sup.14, where R.sup.


 
 
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