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filingDate 1984-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd2bcb0f874817c292fe7745c5420288
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publicationDate 1985-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S60193997-A
titleOfInvention New cyanoimidazole ribonucleoside derivative and its preparation
abstract NEW MATERIAL:A compound of formula I (R 1 , R 2 , R 3 are H, protecting groups for hydroxyls) and its salt. n EXAMPLE: 4-Cyano-1-β-D-ribofuranosylimodazolium-5-oleate. n USE: A carcinostatic agent. n PREPARATION: The deprotection of a compound of formula II (R is protecting group for hydroxyl) such as 4-carbamoyl-1-(2,3,5-tri-O-acetyl)-β-D-ribofuranosyl)- imidazolium-5-oleate is carried out using phosphorus oxychloride, preferably by about 2mol amount to the compound for 2W3hr to give the compound of completely or partially deprotection. n COPYRIGHT: (C)1985,JPO&Japio
priorityDate 1984-03-14-04:00^^<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: 24.