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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-06
filingDate 1969-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fae2310d1607190b581f7d0b4f09af86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2cb5782386c17584d8cd834c7b55d99f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f253bc97dbbef66b21eb785f81d7a1f
publicationDate 1970-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1189973-A
titleOfInvention Cytostatically-Active 2',3'-Didesoxy-3'-Fluoropyrimidine-Nucleosides
abstract 1,189,973. Pyrimidine nucleosides. DEUTSCHE AKADEMIE DER WISSENSCHAFTEN ZU BERLIN. 14 Feb., 1969, No. 8107/69. Heading C2C. Novel, cytoatatically active compounds I wherein X is oxygen, sulphur or imino and R is hydrogen, halogen, hydroxy, mercapto or unsubstituted or substituted alkyl, are obtained by reacting a corresponding pyrimidine nucleoside, appropriately substituted on the oxygen of the 3<SP>1</SP>-hydroxy group, with a fluoronation agent. 2<SP>1</SP>,3<SP>1</SP>-Didehydro-3<SP>1</SP>-desoxy-thymidine is prepared by treating 1-(2<SP>1</SP>,3<SP>1</SP>-didesoxy-3<SP>1</SP>-fluoro- #-D-pentofuranosyl)-thymine (a compound of the invention) with aqueous alcoholic sodium hydroxide solution.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0305117-A3
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5070078-A
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priorityDate 1969-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 28.