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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C33-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C29-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C49-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C29-136
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C29-154
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-136
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-153
filingDate 2014-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2016-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101644016-B1
titleOfInvention A method for preparing optically active 3-amino-1-phenylpropanol derivatives as an intermediate and a method for preparing optically active pharmaceutical products using the same
abstract The present invention relates to a process for the preparation of an optically active ( R ) or ( S ) enantiomeric excess ( ee ) having an enantiomeric excess ( ee ) of at least 80%, comprising asymmetric reduction reaction in the presence of a spiroborate ester catalyst and a hydrogen donor. Amino-1-phenylpropanol derivative having the formula (I); And ( R ) - or ( S ) -3-amino-1-phenylpropanol derivatives which are intermediates using the catalyst.
priorityDate 2014-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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