Synthesis and antiviral evaluation of 2'-deoxy-4'-thio-L-nucleosides and their phosphotriester derivatives bearing S-acyl-2-thioethyl bioreversible phosphate-protecting groups

Article abstract of DOI:10.1080/07328319808004318

A new route to 2-deoxy-4-thio-L-ribofuranose and the synthesis of some 4'-thio-L-nucleosides are reported. Also, the bis(SATE) phosphotriester derivatives of 2'-deoxy-4'-thio-L-cytidine and -adenosine were synthesized and their biological activities are discussed.

Full text of DOI:10.1080/07328319808004318

Nucleosides and Nucleotides
ISSN: 0732-8311 (Print) (Online) Journal homepage: http://www.tandfonline.com/loi/lncn19
Synthesis and Antiviral Evaluation of 2′-Deoxy-4′-
thio-L-nucleosides and Their Phosphotriester
Derivatives Bearing S-Acyl-2-thioethyl
Bioreversible Phosphate-Protecting Groups
F. De Valette , J.-L. Barascut & J.-L. Imbach
To cite this article: F. De Valette , J.-L. Barascut & J.-L. Imbach (1998) Synthesis and Antiviral
Evaluation of 2′-Deoxy-4′-thio-L-nucleosides and Their Phosphotriester Derivatives Bearing
S-Acyl-2-thioethyl Bioreversible Phosphate-Protecting Groups, Nucleosides and Nucleotides,
17:12, 2289-2310, DOI: 10.1080/07328319808004318
To link to this article: http://dx.doi.org/10.1080/07328319808004318
Published online: 16 Aug 2006.
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Date: 30 October 2015, At: 23:31