http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101446017-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J23-464
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D291-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D291-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-46
filingDate 2012-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2014-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101446017-B1
titleOfInvention Method for the stereoselective preparation of 4-alkyl-5-aryl 5-membered ring sulfamidates
abstract The present invention relates to a novel process for the simple and efficient synthesis of 4-alkyl-5-aryl 5-membered ring sulfamidates having a high optical purity, Alkyl-5-aryl 5-membered ring sulfimidate stereoisomer compound having high optical activity by carrying out asymmetric reduction using a cyclic imine compound with a chiral organotitanium catalyst and a hydrogen donor do.
priorityDate 2012-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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