http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H09124612-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6c8d4dc7bd1a30d8fda907fceaeb4e69
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
filingDate 1995-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e945efb151db48a3c9f067a9cf69ca95
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ec0473597dfc51237a35c5cda846894
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af0cdc454fd13ddb8f8d62493794cf56
publicationDate 1997-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H09124612-A
titleOfInvention Method for producing acyclonucleoside
abstract (57) Abstract: Formula (1) ## STR1 ## W-CH 2 -O- (CH 2 ) 2 -O-COCH 3 ... (1) ( wherein, W is substituted The present invention provides a new method for producing an acyclonucleoside represented by 1-pyrimidinyl group or optionally 9-purinyl group). SOLUTION: The base represented by the general formula (2): WH (2) (wherein W is the same as in the formula (1)) is silylated and then in the presence of iodotrimethylsilane or chloro. In the presence of trimethylsilane and a metal iodide compound, 2- React with acetoxyethyl acetoxymethyl ether. Instead of the silylation in advance, the reaction may be carried out in the presence of a silylating agent.
priorityDate 1995-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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