http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H06340674-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B53-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B43-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F5-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-27
filingDate 1993-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d13a5591e9db3723950380fefc0c5835
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4eaf2f347eddf7d79d77821767276926
publicationDate 1994-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H06340674-A
titleOfInvention Optically active oxazaborolidine
abstract (57) [Summary] [Structure] General formula [I] (Chemical formula 1) (In the formula, R 1 represents an alkyl group, an allyl group, an aryl group, an aralkyl group or a halogen atom, and R 2 and R 3 are the same or different and each represents an alkyl group, an aryl group or an aralkyl group, and * represents an asymmetric carbon. ) Optically active oxazaborolidine represented by By using the asymmetric reducing agent obtained from the optically active oxazaborolidine derivative [I] of the present invention and a borohydride compound, it is possible to efficiently produce optically active amines with high optical purity. Is possible.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6020495-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5750713-A
priorityDate 1993-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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