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filingDate 1992-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b298c6d40c5e10c50bb9418da65b7ce9
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publicationDate 1995-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5416204-A
titleOfInvention Method for preparing 2'-3'-dideoxy-β-nucleosides using 2,2-dideoxy-di(organothio)-pentofuranose intermediates
abstract 2,3-Dideoxy-2,2-di(organothio)-B-D-pentofuranosyl-pyrimidines are disclosed as intermediates in the synthesis of 2', 3'-dideoxynucleosides and have the structure shown below. ##STR1## wherein R 4 is a hydroxyl protecting group; n X is oxygen or nitrogen, said nitrogen being bonded to a hydrogen atom, an alkyl or acyl group; n Y is hydrogen, halogen, alkyl, haloalkyl or haloalkenyl; and n R 5 is alkyl, aralkyl, or aryl wherein aralkkyl or aryl is substituted with hydrogen, halogen, nitro or alkoxy. n 2', 3'-Dideoxynucleosides, products of the above intermediates, are useful as antiviral agents.
priorityDate 1991-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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