http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2003246770-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_129e393582e6bdf4029baf2206522f45
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B53-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-44
filingDate 2002-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7a9c9c565b3a616faa83711f35200b63
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa4975fa8c3c2668188ed6fba7189df5
publicationDate 2003-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2003246770-A
titleOfInvention Production method of optically active substance
abstract [PROBLEMS] To obtain a useful optically active compound having a plurality of asymmetric centers by mildly and highly selectively opening an achiral cyclic compound having a symmetric structure in a stereoselective manner. . An optically active compound is obtained by reacting an amine nucleophilic reagent in the presence of a bidentate active species having a tartaric acid derivative as a ligand to stereoselectively open a cyclic substrate having a symmetric structure. A method for producing an optically active substance, characterized by obtaining: As the amine nucleophile, aniline, benzylamine, phenylethylamine and the like are preferable, and as the tartaric acid derivative serving as a ligand, L-tartaric acid dibenzylamide and the like are preferably used.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11767337-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11697666-B2
priorityDate 2002-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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