4.5 Article

Straightforward synthesis of triazoloacyclonucleotide phosphonates as potential HCV inhibitors

Journal

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume 20, Issue 24, Pages 7365-7368

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2010.10.046

Keywords

Antiviral; Click chemistry; Nucleotides analogues; HCV

Funding

  1. Comite Mixte Inter-universitaire Franco-Marocain Programme [MA/06/143]

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Preparation of several triazoloacyclic nucleoside phosphonates is described. The key step of the synthesis involves a copper(I)-catalysed azide-alkyne 1,3-dipolar cycloaddition between azidoalkylphosphonates and propargylated nucleobases. The antiviral properties of these new analogues have been evaluated and revealed interesting potencies. (C) 2010 Elsevier Ltd. All rights reserved.

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