Trifluoromethyl derivatives of canonical nucleosides: synthesis and bioactivity studies

Abstract

The use of the system CF₃SO₂Na/tert-butyl-hydroperoxide (tert-ButOOH), recently reported for the efficient trifluoromethylation of a variety of heterocyclic aromatic compounds, has been here profitably exploited for the synthesis of 5-CF₃-2′-deoxycytidine, 8-CF₃-2′-deoxyadenosine, 8-CF₃-2′-deoxyguanosine and 8-CF₃-inosine, regioselectively obtained in good to acceptable yields following a very simple protocol. The bioactivity of these modified nucleosides, and particularly of the novel 8-CF₃-2′-deoxyguanosine and 8-CF₃-inosine, has been evaluated on a panel of tumour and non-tumour cell lines in preliminary in vitro cytotoxicity assays.