http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103664976-B

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F5-025
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P41-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P17-181
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-0285
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
filingDate 2013-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2015-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103664976-B
titleOfInvention The preparation method of a kind of cis hexahydro furyl also [2,3-b] furan-3-ol
abstract The present invention relates to a kind of novel chirality non-metallic catalyst and catalyze and synthesize cis hexahydro furyl also [2,3-b] method of furan-3-ol, the method is with 2,3-dihydrofuran and glycollic aldehyde dimer are raw material, under the catalysis of chirality non-metallic catalyst oxazaborolidine positive ion, obtain cis hexahydro furyl also [2,3-b] furan-3-ol; The highly selective acylation of this furan alcohol under enzyme catalysis, can be separated further and obtain (3R, 3AS, 6AR)-hexahydro furyl also [2,3-b] furan-3-ol.The inventive method is compared with existing method, more convenient, green, economical.
priorityDate 2013-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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