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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4e697fd7e4e38671846d9735bde3ed02
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H13-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H13-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-04
filingDate 2007-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9ccab4d7ee59fd94fde3d0fba5ceca0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1be9f1483de166d9e350743196f1e603
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7101a4498083bcf722b9a945ab0dcf4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4b25fa98afd2dd4069b8eb860f585b74
publicationDate 2009-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101595117-A
titleOfInvention The manufacture method of furanose derivative
abstract The purpose of this invention is to provide highly selective, with high yield, make the β-anomeric method of ribofuranose derivatives with the method that is suitable for industry.According to the present invention; the manufacture method of ribofuranose derivatives can be provided; it is characterized in that; 2; 3,5-three-O-acyl group-1-O-alkyl-ribofuranose and 2 is in the acetolysis reaction of 3-two-O-acyl group-1-O-alkyl-5-desoxyribofu-; by the consumption and/or the use poor solvent of conditioned reaction reagent, thereby in the furanose derivative that is generated, β-anomer is separated out.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112300226-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111484535-A
priorityDate 2006-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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