Synthesis and antiviral evaluation of unnatural β-L-enantiomers of 3'- fluoro- and 3'-azido-2',3'-dideoxyguanosine derivatives

Article abstract of DOI:10.1080/15257770008033004

3'-Fluoro-2',3'-dideoxy- (3) and 3'-azido-2',3'-dideoxy- (4) β-L- ribofuranonucleoside derivatives of guanine have been synthesized and their antiviral properties examined. All these derivatives were regioselectively and stereospecifically prepared by gly

Full text of DOI:10.1080/15257770008033004

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Synthesis and Antiviral Evaluation of
Unnatural β-L-Enantiomers of 3′-Fluoro-
and 3′-Azido-2,3′-dideoxyguanosine
Derivatives
Arnaud Marchand a , Christophe Mathé a , Jean-Louis Imbach a
Gilles Gosselin a
&
a Laboratoire de Chimie Organique Biomoléculaire de Synthèse,
U.M.R. CNRS 5625, Université de Montpellier II, Sciences et
Techniques du Languedoc , 34095, Montpellier Cedex 5, France
Published online: 24 Sep 2006.
To cite this article: Arnaud Marchand , Christophe Mathé , Jean-Louis Imbach & Gilles Gosselin (2000)
Synthesis and Antiviral Evaluation of Unnatural β-L-Enantiomers of 3′-Fluoro- and 3′-Azido-2,3′-
dideoxyguanosine Derivatives, Nucleosides, Nucleotides and Nucleic Acids, 19:1-2, 205-217, DOI:
10.1080/15257770008033004
To link to this article: http://dx.doi.org/10.1080/15257770008033004
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