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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_01f1be48d9b96a3bcc32fa862d9fad31
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-273
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-273
filingDate 2011-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81d8534d314e253038bc239c51040088
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_98fa5c4545716b0e742196801f2abbcb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d2475e4e7cea57c2a369d73a97e490ae
publicationDate 2014-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8912345-B2
titleOfInvention Method for preparing optically pure (−)-clausenamide compound
abstract Disclosed in the present invention is a method for preparing a (−)-clausenamide compound of formula (I), comprising: firstly, catalyzing the asymmetrical epoxidation of trans-cinnamate using a chiral ketone derived from fructose or a hydrate thereof as a catalyst, and then subjecting the product to amidation, oxidation, cyclization and reduction successively to finally obtain the optically pure (−)-clausenamide compound of formula (I).
priorityDate 2011-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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