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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2b3c1be84d2fa419cfc5ad68846dd174
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-06
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H3-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H9-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-06
filingDate 1998-01-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e92f9d56c935ca0bee7d57ca79e547e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a3f3b8bc40fd1ec59505508b28c4323
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_edd2dba4a473d445ce73fdb74c9db125
publicationDate 2000-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100247505-B1
titleOfInvention Method for preparing 2'-fluoro-5-methyl-β-L-arabinofuranosyluridine
abstract The present invention is directed to 2'-fluoro-5 represented by the following Chemical Formula 1, which exhibits strong antiviral activity against antiviral activity, in particular hepatitis B-virus and Epstein-Bar virus. A novel and improved process for preparing -methyl-β-L-arabinofuranosyluridine is provided.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100976778-B1
priorityDate 1997-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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