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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3970ff2929243c84b2f197df598b9c59
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-06
filingDate 2011-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dfadffd7f681647e8352b8e9e928a794
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3ab79de72453abdfd3ca39a92fd8951
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c6418739e3709a1d261c138eed2e077
publicationDate 2015-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102180886-B
titleOfInvention Asymmetric catalytic synthesis method for Galanthamine
abstract The invention discloses an enantioselectivitiy synthesis method for Galanthamine. The method comprises the following steps of: performing enantioselectivitiy Michael addition reaction on Vanillin serving as a starting raw material to obtain a key intermediate; and performing twelve-step reaction to obtain optical pure (-)-Glanthamine.
priorityDate 2011-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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