A series of 1,3-oxathiolane-based nucleoside analogues 5-methyl substituted was synthesized and tested as potential antiviral agents. Structural characterization and C2-C4 / C2-C5 relative stereochemistry assignments were performed by NMR experiments. All tested isomers were found to be inactive and cytotoxic.

Synthesis of 5-Methyl-1,3-oxathiolane-based Nucleoside Analogues as Potential Antiviral Agents / Franchini, Silvia; Tait, Annalisa; Sorbi, Claudia; Brasili, Livio. - In: MEDICINAL CHEMISTRY. - ISSN 1573-4064. - STAMPA. - 8:(2012), pp. 769-778. [10.2174/157340612802084162]

Synthesis of 5-Methyl-1,3-oxathiolane-based Nucleoside Analogues as Potential Antiviral Agents

FRANCHINI, Silvia;TAIT, Annalisa;SORBI, Claudia;BRASILI, Livio
2012

Abstract

A series of 1,3-oxathiolane-based nucleoside analogues 5-methyl substituted was synthesized and tested as potential antiviral agents. Structural characterization and C2-C4 / C2-C5 relative stereochemistry assignments were performed by NMR experiments. All tested isomers were found to be inactive and cytotoxic.
2012
8
769
778
Synthesis of 5-Methyl-1,3-oxathiolane-based Nucleoside Analogues as Potential Antiviral Agents / Franchini, Silvia; Tait, Annalisa; Sorbi, Claudia; Brasili, Livio. - In: MEDICINAL CHEMISTRY. - ISSN 1573-4064. - STAMPA. - 8:(2012), pp. 769-778. [10.2174/157340612802084162]
Franchini, Silvia; Tait, Annalisa; Sorbi, Claudia; Brasili, Livio
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/744581
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