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5994560 |
Resolution of racemic mixtures using polymers containing chiral units
Described herein is a novel process to resolve a racemic compound into its optically active isomers without need for chemical transformation such as salt formation. The process advantageously...
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5892112 |
Process for preparing synthetic matrix metalloprotease inhibitors
Synthetic mammalian matrix metalloprotease inhibitors are disclosed that are useful for treating or preventing diseases wherein said diseases are caused by unwanted mammalian matrix metalloprotease...
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5329014 |
Method for recovering optically active tryptophan
Optically active tryptophan of high purity can be obtained in high yields from a tryptophan fermentation broth, using crystallization of optically active tryptophan hydrochloride in combination...
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4978759 |
Process for the stereospecific synthesis of optically pure 4-amino-3-hydroxycarboxylic acid derivatives
The process described makes it possible to obtain optically pure 4-amino-3-hydroxycarboxylic acids by means of a series of stereoselective steps. The starting material is an alpha-amino acid in the...
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4918196 |
Process for recimization of an optically active alpha-amino acid amides and process for producing optically active alpha-amino acids
A process for optically isomerizing an optically active alpha-amino acid amide comprising heating a D-alpha-amino acid amide or an L-alpha-amino acid amide in the presence of a strongly basic...
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4904654 |
7-chloro-5,6-dihydro-3-(5-(2-hydroxy-isoprop yl)-1,2,4-oxadiazol-3-yl)-5-methyl-6-oxo-4H-imidazo[1,5a][1,4]benzodiazep ine
A metabolite of the known anxiolytic agent, 7-chloro-5,6-dihydro-3-(5-isopropyl-1,2,4-oxadiazol-3-yl)-5-
methyl-6-oxo-4 H- imidazo[1,5a][1,4]benzodiazepine is a 2-hydroxy derivative of the...
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4772599 |
Benzodiazepine derivatives and their preparation and use
New benzodiazepine derivatives of the general formula ##STR1## wherein X 1 and X 2 independently are ##STR2## wherein R 1 is C 1 -3 -alkyl, C 3 -5 -cycloalkyl, C 1 -3 -alkoxymethyl, C 1 -3...
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4718994 |
Method for preparing hydroxy compounds of aromatic and heteroaromatic series
A method for perparing hydroxy compounds of the aromatic and heteroaromatic series of the general formula: ##STR1## wherein when R 1 --COOH, --CH 2 CH(NH 2 )COOH then R 2 --OH, --H,...
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4713470 |
Racemization of amino acids
There is disclosed a process for the racemization of amino acids and derivatives thereof. The racemization process of the present invention uses an aromatic aldehyde-containing polymer made from...
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4610827 |
Amino acid complex and a method for optical resolution of a DL-amino acid
A method for optical resolution of a DL-amino acid comprising reacting the DL-amino acid with an optically active N-acyl aspartic acid in a solvent or mixture of solvents, and separating the...
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4602096 |
Process for the racemization of N-acetyl-D,L-α-aminocarboxylic acids
N-acetyl-D(L)-α-aminocarboxylic acids are thermally racemized by melting, adding a small amount of acetic anhydride to the melt and heating to a temperature between the melting temperature and...
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4588818 |
Method for recovery of optically active tryptophane
A method for recovery of optically active tryptophane, which comprises filtering a solution of optically active tryptophane containing impurities through a semi-permeable membrane; adding a lower...
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4540792 |
Process for the preparation of a free L α-amino acid
This invention relates to a process for the preparation of free L α-amino acids by the complete conversion of their D antipodes taken individually or possibly in racemic mixtures. The process...
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4519955 |
Method for optical resolution of DL-α-amino acid or (±)-α-phenylethanesulfonic acid
α-(S)-amino acid.α-phenylethanesulfonate compounds and methods of optical resolution of α-amino acids and α-phenylethanesulfonic acids are described.
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4481362 |
Process for preparing optically active tryptophanes
Biochemical optical resolution of DL-tryptophanes in which DL-tryptophane amides are interacted with the culture products, or their treated products, of a microorganism capable of producing amidase...
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4440936 |
Rhodium-phosphine chiral hydrogenation catalysis of acetophenone, atropic acid, and alpha-acylamidoacrylic acids and esters thereof
The chiral phosphine ligand (R)-1,2-bis(diphenylphosphino)-1-cyclohexylethane, when complexed to Rh(I), functions as a superior chiral hydrogenation catalyst. The chiral phosphine ligand is more...
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4379941 |
Resolution of racemic amino acids
Racemic amino acids can be readily resolved by conversion to their diastereomeric esters of an optically active 2-isopropyl-5-methylcyclohexanol and separating the diastereomers by chromatography....
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4275217 |
Process for the preparation of optically active α-amino acids and their derivatives
A chiral α-amino acid having a hydrogen substituent in a position alpha to the carboxylic function thereof is prepared by subjecting a corresponding optical antipode with a chiral amino acid to a...
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4124533 |
Metal coordination complexes containing optically active phosphine or arsine ligands
Process for the homogeneous catalytic hydrogenation of β-substituted-α-acylamido-acrylic acids which yields, after hydrogenation, an optically active mixture. The process comprises the...
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4072698 |
Resolution of aminonitriles
The present invention is a chemical method for obtaining an optically pure 2-aminonitrile or a 2-aminoamide from (1) an optically impure mixture, (2) a racemic mixture, or (3) the optically pure...
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4072691 |
Process for the resolution of DL-6-chlorotryptophan
Seed crystals of one optically active enantiomer of 6-chlorotryptophan methanesulfonate or 6-chlorotryptophan benzenesulfonate are added to a supersaturated solution of DL-6-chlorotryptophan...
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3991077 |
Method of racemizing optically active N-acylamino acids
Optically active amino acids N-acylated with carboxylic acids are readily racemized without decomposition at elevated temperature in inert organic solvents in which they are homogeneously soluble...
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3976680 |
Production of an ester of one enantiomer of an α-amino acid in the form of a salt with an optically active acid
A process for the production of an ester of one enantiomer of an α-amino acid in the form of a salt with an optically active acid, which comprises reacting an ester of the opposite enantiomer of...
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3904646 |
Resolution of tryptophan using benzenesulfonic acid and p-phenolsulfonic acid
Seed crystals of one optically active enantiomer of tryptophan benzenesulfonate or tryptophan p-phenolsulfonate are added to a supersaturated solution of DL-tryptophan benzenesulfonate or...
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3901915 |
Optical resolution of organic carboxylic acids
Racemic organic carboxylic acids are efficiently resolved into their enantiomers with antipodes of α-methyl-p-nitrobenzylamine.
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3869472 |
3-Indolyl aliphatic acid derivatives
N-acylated 3-indolyl acetic acid derivatives having anti-inflammatory, analgesic, antipyretic and anti-cholesterolemic activities and being useful as an intermediate for anti-inflammatory drugs...
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3532684 |
MOLECULAR COMPOUNDS OF INOSINE AND TRYPTOPHAN
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3527671 |
PROCEDURE FOR THE SEPARATION OF ISOTOPECONTAINING AMINO ACID RACEMATES INTO THEIR OPTICAL D- AND L-ANTIPODES
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3480645 |
PROCESS FOR OPTICAL RESOLUTION OF RACEMIC PANTOLACTONE
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3381031 |
Resolution of racemic amino acids
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3213106 |
Process of racemizing optically active alpha acids
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3168527 |
1-aryl-5-(p-fluorophenyl)-pyrrole-2-propionic acid compounds
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3167566 |
Resolution of dl-tryptophane and dl-alpha-phenylethylamine
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3149122 |
Resolution of ammonium nu-acyl-dltryptophanates
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3094537 |
Resolution of acetyl-di-tryptophan
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3056799 |
Processes and intermediate products
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3028430 |
Process for the production of optically active isomers of amphetamine
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3028395 |
Process for the resolution of optically active acids
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2957917 |
Resolution of organic compounds and apparatus therefor
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2957886 |
Resolution procedures and apparatus therefor
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2865928 |
Resolution of n-acyl-dl-tryptophans
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2813876 |
Resolution of tryptophane derivatives
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2797226 |
Process of resolving dl-acyl tryptophan compounds and products obtained thereby
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3825559 |
Title is not available
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