A novel reagent for regioselective cleavage of 2,3-epoxyalcohols by fluoride - a synthesis of 3-fluoro-293-dideoxy-d-erythro-pentose.
- 17 November 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (47) , 7087-7088
- https://doi.org/10.1016/s0040-4039(00)60842-0
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Fluorinated sugar analogs of potential anti-HIV-1 nucleosidesJournal of Medicinal Chemistry, 1991
- Compounds of (i-PrO)3 TiX as novel reagents for regioselective oxirane ring openingTetrahedron: Asymmetry, 1991
- Structure-activity relationships of fluorinated nucleoside analogs and their synergistic effect in combination with phosphonoformate against human immunodeficiency virus type 1Antimicrobial Agents and Chemotherapy, 1989
- Asymmetric synthesis and structural analysis of 5-O-benzoyl-2,3-dideoxy-3-fluoro-.alpha.,.beta.-D-ribofuranose and -xylofuranose from homochiral 1-fluoro-3-sulfinylacetoneThe Journal of Organic Chemistry, 1989
- Anti-retrovirus activity of 3′-fluoro- and 3′-azido-substituted pyrimidine 2′,3′-dideoxynucleoside analoguesBiochemical Pharmacology, 1988
- Enhanced In Vitro Inhibition of HIV-1 Replication by 3′-Fluoro-3′-deoxythymidine Compared to Several Other Nucleoside AnalogsAIDS Research and Human Retroviruses, 1988
- 3'-Substituted 2',3'-dideoxynucleoside analogs as potential anti-HIV (HTLV-III/LAV) agentsJournal of Medicinal Chemistry, 1987
- Tetrahedron report number 221Tetrahedron, 1987
- Methyl 5-O--butyldiphenylsilyl-2-deoxy-D-threo-pentofuranoside; an approach to the syntesis of 3′-substituted-2′,3′-dideoxynucleosides including 3′-azido-3′-deoxythymidine and of 3′-substituted-2′,3′-dideoxy-C-nucleosidesTetrahedron Letters, 1987
- Nucleoside von Fluorzuckern; Aufspaltung des Epoxidringes von 1‐(5‐O‐Benzoyl‐2,3‐epoxy‐β‐D‐lyxofuranosyl)‐uracil mit FluorwasserstoffsäureZeitschrift für Chemie, 1975