Synthesis of ribavirin 2'-Me-C-nucleoside analogues
Fanny Cosson1, Aline Faroux1, Jean-Pierre Baltaze2
1Laboratoire de Chimie Biologique, University of Cergy-Pontoise, 5 mail Gay-Lussac, Cergy-Pontoise, France.
Beilstein Journal of Organic Chemistry
|May 16, 2017
Abstract:
An efficient synthetic pathway leading to two carbonated analogues of ribavirin is described. The key-steps in the synthesis of these ribosyltriazoles bearing a quaternary carbon atom in the 2'-position are an indium-mediated alkynylation and a 1,3-dipolar cyclization.
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