170114-35-9Relevant articles and documents
Synthesis and anti-HIV activity of C4-modified pyrimidine nucleosides
Wallis, Mark P.,Mahmood, Naheed,Fraser, William
, p. 83 - 89 (1999)
One-pot syntheses provided a series of triazole- and pentafluorophenyloxy-substituted pyrimidine nucleosides. Most of the compounds in the series displayed anti-HIV activities but none as potent as AZT 2. 1-(β-D-Erythro-pentofuranosyl)-4-pentafluorophenyloxy-2(1H)-pyrimidinone 14 was the most potent and the most selective compound in the series with EC50 = 1.6 μM.