Simple and Stereoselective Syntheses of Nucleoside Analogues with a Benzo[c]furan Glycone Moiety
- 1 April 1999
- journal article
- research article
- Published by Taylor & Francis in Nucleosides and Nucleotides
- Vol. 18 (4-5) , 559-563
- https://doi.org/10.1080/15257779908041494
Abstract
A series of d4T analogues have been synthesised in which the 2′,3′-didehydro-2′,3′-dideoxyribose moiety is replaced by a benzo[c]furan core. A simple strategy has been developed to access a range of compounds for biological screening. In addition, a stereoselective approach has been achieved with view to permit more detailed studies.Keywords
This publication has 8 references indexed in Scilit:
- Catalytic Asymmetric DihydroxylationChemical Reviews, 1994
- Toward an Understanding of the High Enantioselectivity in the Osmium-Catalyzed Asymmetric Dihydroxylation (AD). 1. KineticsJournal of the American Chemical Society, 1994
- Synthesis and Anticancer and Antiviral Activity of Certain Pyrimidine Nucleoside AnaloguesPublished by Springer Nature ,1993
- Nucleosides and Nucleotides as Antitumor and Antiviral AgentsPublished by Springer Nature ,1993
- AIDS-driven nucleoside chemistry.Chemical Reviews, 1992
- 1-Methoxyisobenzofuran from base-induced and acid-catalyzed reactions of 1,3-dihydro-1,3-dimethoxyisobenzofuranThe Journal of Organic Chemistry, 1987
- 4-(1,2,4-Triazol-1-yl)- and 4-(3-nitro-1,2,4-triazol-1-yl)-1-(β-D-2,3,5-tri-O-acetylarabinofuranosyl)pyrimidin-2(1H)-ones. Valuable intermediates in the synthesis of derivatives of 1-(β-D-arabinofuranosyl)cytosine (ara-C)Journal of the Chemical Society, Perkin Transactions 1, 1982
- Interproton spin-spin coupling across a dual path in 2,5-dihydrofurans and phthalansJournal of the American Chemical Society, 1975