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filingDate 1992-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_456a3e90cd66633c5e90880ee25ec03c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf32bd9f066aa64a5f11aa2219dc058b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f76a14766fcf739e1b9b70e4ebb6fb71
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_792e6efc50af1de97025fc24790182d5
publicationDate 1999-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2140925-C1
titleOfInvention Method of diastereoselective synthesis of nucleosides, intermediate compounds, and method of preparing intermediate compounds
abstract FIELD: chemical industry. SUBSTANCE: described is diastereoselective method of preparing optionally active cis-nucleoside and its analogues or derivatives of formula (I): wherein W,R 1 ,R 2 •X are as defined in claim 1. Purine or pyrimidine base or its analogue or derivative is subjected to glycolization with intermediate compound of formula IIa: or IIb: wherein R 3 L are as defined in claim 1 using Lewis acid in formula III: wherein R 5 -R 8 are as defined in claim 1 followed by reducing R 3 glycolized purine or pyrimidine base or its analogue or derivative. EFFECT: simplified process. 32 cl, 3 ex
priorityDate 1991-05-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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