Synthesis and anti-HIV activity of l-2′-fluoro-2′,3′-unsaturated purine nucleosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. PHASE I STUDIES OF 2',3'-DIDEOXYCYTIDINE IN SEVERE HUMAN IMMUNODEFICIENCY VIRUS INFECTION AS A SINGLE AGENT AND ALTERNATING WITH ZIDOVUDINE (AZT)
2. In Vivo Activity Against HIV and Favorable Toxicity Profile of 2′,3′-Dideoxyinosine
3. Potent and selective in vitro activity of 3' -deoxythymidin-2'-ene (3'-deoxy-2',3'-didehydrothymidine) against human immunodeficiency virus
4. The separated enantiomers of 2'-deoxy-3'-thiacytidine (BCH 189) both inhibit human immunodeficiency virus replication in vitro
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1. L-Nucleosides;Chemical Synthesis of Nucleoside Analogues;2013-02-15
2. ChemInform Abstract: Synthesis and Anti-HIV Activity of L-2′-Fluoro-2′,3′-Unsaturated Purine Nucleosides.;ChemInform;2010-06-19
3. Recent advances in the synthesis of fluorinated nucleosides;Tetrahedron;2010-01
4. Scope and limitations of the Julia–Kocienski reaction with fluorinated sulfonylesters;Tetrahedron;2009-05
5. Fluorinated nucleosides: Synthesis and biological implication;Journal of Fluorine Chemistry;2008-09
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