A novel reagent for regioselective cleavage of 2,3-epoxyalcohols by fluoride - a synthesis of 3-fluoro-293-dideoxy-d-erythro-pentose.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Enhanced In Vitro Inhibition of HIV-1 Replication by 3′-Fluoro-3′-deoxythymidine Compared to Several Other Nucleoside Analogs
2. Structure-activity relationships of fluorinated nucleoside analogs and their synergistic effect in combination with phosphonoformate against human immunodeficiency virus type 1
3. Anti-retrovirus activity of 3′-fluoro- and 3′-azido-substituted pyrimidine 2′,3′-dideoxynucleoside analogues
4. 3'-Substituted 2',3'-dideoxynucleoside analogs as potential anti-HIV (HTLV-III/LAV) agents
5. Fluorinated sugar analogs of potential anti-HIV-1 nucleosides
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1. ChemInform Abstract: A Novel Reagent for Regioselective Cleavage of 2,3-Epoxy Alcohols by Fluoride. A Synthesis of 3-Fluoro-2,3-dideoxy-D-erythro-pentose.;ChemInform;2010-08-20
2. Recent Progress in Synthesis and Applications of Fluorinated Carbohydrates;Current Organic Chemistry;2010-05-01
3. Selective introduction of a fluorine atom into carbohydrates and a nucleoside by ring-opening fluorination reaction of epoxides;Journal of Fluorine Chemistry;2006-07
4. Cleavage of the Epimines of 1,6-Anhydrohexoses with Fluoride Anion;Collection of Czechoslovak Chemical Communications;2005
5. Hybrid Reagent of Ammonium Hydrogen Fluoride and Scandium Triflate: Highly Efficient Catalyst for Ring-opening Fluorination of 2,3-Epoxyalcohols;Chemistry Letters;2004-06
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