http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108558882-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D473-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D473-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D473-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D473-34
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-00
filingDate 2018-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2020-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108558882-B
titleOfInvention Method for synthesizing chiral five-membered carbocyclic purine nucleoside through [3+2] cycloaddition based on allenoic acid ester
abstract The invention discloses a method for synthesizing chiral five-membered carbocyclic purine nucleoside by [3+2] cycloaddition based on allenoic acid ester, belonging to the field of asymmetric synthesis in organic chemistry. α -purine-substituted acrylate 1 and allenoic acid ester 2 are used as raw materials, chiral STICP is used as a catalyst, chiral five-membered carbocyclic nucleoside 3 is obtained after reaction, the reaction enantioselectivity is good, the yield is medium to excellent, the chiral five-membered carbocyclic nucleoside 3 is reduced under the condition of sodium borohydride to obtain monoalcohol five-membered carbocyclic purine nucleoside 4, and then DIBA L-H is adopted for reduction to obtain diol five-membered carbocyclic purine nucleoside 5.
priorityDate 2018-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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