http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1856028-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d202e9e866984fe229f6facc38f1d740
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-32
filingDate 2006-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_741efa7f9c1368ac25812a82842fc4cf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7e145627f87776ea3fc0e84d6ebcd584
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publicationDate 2007-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1856028-A1
titleOfInvention Process to chiral beta amino acid derivatives by asymmetric hydrogenation
abstract The present invention relates to a process for the efficient preparation of enantiomerically enriched beta amino acid derivatives which are useful in the asymmetric synthesis of biologically active molecules. The process comprises an enantioselective hydrogenation of a prochiral beta amino acrylic acid derivative substrate in the presence of an ammonium salt and a transition metal precursor complexed with a chiral ferrocenyl diphosphine ligand.
priorityDate 2005-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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