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filingDate 1990-02-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1993-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b15a2e90e2cfccc8bee9d5454d4c56cf
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publicationDate 1993-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-1809831-C
titleOfInvention Method of dideoxynucleosides synthesis
abstract Use: as an anti-AIDS drug. The inventive product () -4- (6-amino-9H-purin-9-yl) - tetrahydro-2-furan-methanol, BP CioHi3Ns02, so pl. 183-185 ° C, 50% yield; | (3R-cis) -2-amino-1 .E-dihydro-E-Ptetrahydro | 5- {oxymethyl) -3-furanyl 6 N-purin-6-OH, BP CloHiaNsOs, yield 40%, mp. 229-230 ° C. Reagent 1: (2P-trans) -tetrahydro-4 (4-methylphenyl) sulfonyl) oxy-2-furanmethanol. Reagent 2: adenine or guanine. Reaction conditions: in dimethylformamide medium in the presence of 18-crown-b and potassium carbonate. (L C
priorityDate 1989-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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