http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-248028-A3

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_07c273645af222a938f4da0b5465ef9e
filingDate 1984-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a21ae77a0cf53d390235033b591ea5e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3010077ab4b3270e1ae100245167c06d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da05bed206205ed783c052a0cb87c5a7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e8191c050256b7708926e28f1da8a3a
publicationDate 1987-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-248028-A3
titleOfInvention PROCESS FOR THE PREPARATION OF (S) -PHENYLALANINE DERIVATIVES
abstract The invention relates to the improvement of a process for the preparation of (S) -N-acyl-phenylalanines, in particular of the aromatic radical in 3,4-position 0-functionalized derivatives by catalytically asymmetric hydrogenation prochiral unge unsettled precursors in the presence of chiral metal complex catalysts. The hydrogenation products are easy to convert into (S) -phenylalanine or its derivatives. According to the invention, alcohol solvates of a (Z) -2-N-acylamino-3-arylacrylic acid are used as prochiral unsaturated substrates, resulting in optical yields up to when using the particularly suitable cationic rhodium (I) complex catalysts with carbohydrate bis (phosphinic acid esters) as chiral chelate ligands 95% of (S) -N-acyl-3-arylalanine can be achieved even when using high molar ratios of substrate catalyst in excess of one thousand, which was prevented in the case of the previously attempted use of solvate-free substrates by reaction inactivation. As a further advantage, an increase in the reaction rate is achieved in two to ten times.
priorityDate 1984-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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