http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101935302-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_38f6403d850a1fe9e34ef7fd5a010318
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B53-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D221-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
filingDate 2010-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ebf63a2072a3f19b71e249e8fda87e51
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af680eb7943c06bf12d68e229a95f17b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7a42d84dc7e372920d33b8ff4e30b39
publicationDate 2011-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101935302-A
titleOfInvention Asymmetric synthetic method of (-)-huperzine key intermediate
abstract The invention belongs to the field of asymmetric catalysis of organic chemistry, and in particular relates to an asymmetric synthetic method of a (-)-huperzine key intermediate, comprising the following step of: synthesizing a huperzine key intermediate by using an asymmetric Michael/Adol cascade reaction of organic micromolecule catalysis. The asymmetric Michael/Adol cascade reaction is characterized in that the key intermediate (-)-(5S, 9R)-9,10-dihydro-2-methoxyl-7-methyl-11-oxo-5,9-methylene cyclooctane [b] pyridine-5(6H)-methyl carbonate is prepared by using high yield, high optical purity in a gram level.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105017269-A
priorityDate 2010-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2009247754-A1
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID466165366
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID466268057
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID466214160
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID466231714

Total number of triples: 20.