Revaluation of biomass-derived furfuryl alcohol derivatives for the synthesis of carbocyclic nucleoside phosphonate analogues - Université de Montpellier
Article Dans Une Revue Beilstein Journal of Organic Chemistry Année : 2017

Revaluation of biomass-derived furfuryl alcohol derivatives for the synthesis of carbocyclic nucleoside phosphonate analogues

Résumé

The racemic synthesis of new carbocyclic nucleoside methylphosphonate analogues bearing purine bases (adenine and guanine) was accomplished using bio-sourced furfuryl alcohol derivatives. All compounds were prepared using a Mitsunobu coupling between the heterocyclic base and an appropriate carbocyclic precursor. After deprotection, the compounds were evaluated for their activity against a large number of viruses. However, none of them showed significant antiviral activity or cytotoxicity.

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Chimie
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hal-03557540 , version 1 (04-02-2022)

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Bemba Sidi Mohamed, Christian Périgaud, Christophe Mathé. Revaluation of biomass-derived furfuryl alcohol derivatives for the synthesis of carbocyclic nucleoside phosphonate analogues. Beilstein Journal of Organic Chemistry, 2017, 13, pp.251-256. ⟨10.3762/bjoc.13.28⟩. ⟨hal-03557540⟩
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