Revisited 3′-Deoxy-3′-C-Methyl-β-D-Ribonucleoside Series

Mohamed Aljarah; Sarah Couturier; Gilles Gosselin; Christophe Mathé; Christian Périgaud

doi:10.1080/15257770701521730

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Revisited 3′-Deoxy-3′-C-Methyl-β-D-Ribonucleoside Series

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Revisited 3′-Deoxy-3′-C-Methyl-β-D-Ribonucleoside Series

Mohamed Aljarah, Sarah Couturier, Gilles Gosselin, Christophe Mathé et Christian Périgaud

Nucleosides, nucleotides & nucleic acids, Vol.26(8-9), pp.1125-1128

01/01/2007

DOI: https://doi.org/10.1080/15257770701521730

PMID: 18058550

Résumé

glycosylation

Nucleoside

stereoselective synthesis

The synthesis of some 3′-deoxy-3′-C-methylnucleoside analogues bearing naturally occuring nucleic acid bases was achieved from the preparation of a suitable peracylated 3-deoxy-3-C-methyl sugar using a stereoselective pathway. In addition, examples of chemical modifications at the 2′ position are presented.

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Détails

Titre: Revisited 3′-Deoxy-3′-C-Methyl-β-D-Ribonucleoside Series
Créateurs - sans rôle: Mohamed Aljarah - UMR 5625 CNRS-UM II, Université Montpellier II
Sarah Couturier - UMR 5625 CNRS-UM II, Université Montpellier II
Gilles Gosselin - UMR 5625 CNRS-UM II, Université Montpellier II
Christophe Mathé - UMR 5625 CNRS-UM II, Université Montpellier II
Christian Périgaud - UMR 5625 CNRS-UM II, Université Montpellier II
Détails de publication: Nucleosides, nucleotides & nucleic acids, Vol.26(8-9), pp.1125-1128
Éditeur: Taylor & Francis Group
Nombre de pages: 4
Identifiants: 99138908009311
Unité académique: Institut des Biomolécules Max Mousseron - IBMM
Langue: English
Type de ressource: Journal article