Synthesis of (R)- and (S)-ßhydroxyphosphonate acyclonucleosides: structural analogues of Adefovir (PMEA) - Archive ouverte HAL
Article Dans Une Revue Tetrahedron: Asymmetry Année : 2011

Synthesis of (R)- and (S)-ßhydroxyphosphonate acyclonucleosides: structural analogues of Adefovir (PMEA)

Résumé

A synthetic pathway to new acyclonucleoside phosphonates, as analogues of Adefovir, is described. The reduction of an acyclonucleoside ß-ketophosphonate, readly available from the nucleobase and benzyl-acrylate, afforded a mixture of (R)- and (S)-ß-hydroxyphosphonate derivatives which was resolved. The assignment of the absolute configuration was proposed on the basis of NMR studies and was supported by molecular modelling studies.

Domaines

Chimie organique

Dates et versions

hal-00637860 , version 1 (03-11-2011)

Identifiants

Citer

Mahesh Kasthuri, Laurent Chaloin, Christian Perigaud, Suzanne Peyrottes. Synthesis of (R)- and (S)-ßhydroxyphosphonate acyclonucleosides: structural analogues of Adefovir (PMEA). Tetrahedron: Asymmetry, 2011, 22, pp.1505-1511. ⟨10.1016/j.tetasy.2011.08.010⟩. ⟨hal-00637860⟩
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