Synthesis and antiviral evaluation of the β-L-enantiomers of some thymine 3′-deoxypentofuranonucleoside derivatives

Article abstract of DOI:10.1080/15257770008045443

3′-Deoxy-β-L-erythro- (3), 3′-deoxy-β-L-threo- (6), 2′-fluoro- (7) and 2′-azido-2′,3′-dideoxy-β-L-erythro- (10) pentofuranonucleoside derivatives of thymine have been synthesized and their antiviral properties examined. All these derivatives were stereosp

Full text of DOI:10.1080/15257770008045443

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Synthesis and Antiviral Evaluation of the
β-L-Enantiomers of Some Thymine 3′-
Deoxypentofuranonucleoside Derivatives
Christophe Mathé a & Gilles Gosselin b
a Laboratoire de Chimie Organique Biomoléculaire de Synthèse,
U.M.R. 5625 CNRS-UM-II and Laboratoire Coopératif NOVIRIO-CNRS-
UM II
b Université Montpellier II, Sciences et Techniques du Languedoc,
34095, Montpellier Cedex 5, France
Version of record first published: 17 Apr 2008.
To cite this article: Christophe Mathé & Gilles Gosselin (2000): Synthesis and Antiviral Evaluation
of the β-L-Enantiomers of Some Thymine 3′-Deoxypentofuranonucleoside Derivatives, Nucleosides,
Nucleotides and Nucleic Acids, 19:10-12, 1517-1530
To link to this article: http://dx.doi.org/10.1080/15257770008045443
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