Nucleosides and Nucleotides vol. 18, no. 4-5, pp. 571 - 572
Indexed
SCOPUS
Document Type
Conference Paper
Abstract
L-2'-Deoxy-2'-up-fluoro-4'-thionucleosides were efficiently synthesized from D-xylose via L-4-thioarabitol derivative as a key intermediate and evaluated for antiviral activities against HIV-1, HSV-1,2 and HBV.