This review offers an overview of the synthesis of phosphonated isoxazolidinyl nucleo-sides, a new class of interesting and potentially antiviral/antitumor agents. The synthetic methodology relies on a 1,3-dipolar cycloaddition reaction as a key step. The cycloaddi-tion process involves substituted nitrones, phosphonated nitrones, or nitrones containing functional groups easily convertible into a phosphonated group. Biological assays are pre-sented, which show that phosphonated isoxazolidinyl nucleosides represent a new prom-ising template of nucleoside analogues.

PHOSPHONATED ISOXAZOLIDINYL NUCLEOSIDES, A NEW CLASS OF MODIFIED NUCLEOSIDES

GIOFRE', Salvatore Vincenzo;ROMEO, Roberto;
2014-01-01

Abstract

This review offers an overview of the synthesis of phosphonated isoxazolidinyl nucleo-sides, a new class of interesting and potentially antiviral/antitumor agents. The synthetic methodology relies on a 1,3-dipolar cycloaddition reaction as a key step. The cycloaddi-tion process involves substituted nitrones, phosphonated nitrones, or nitrones containing functional groups easily convertible into a phosphonated group. Biological assays are pre-sented, which show that phosphonated isoxazolidinyl nucleosides represent a new prom-ising template of nucleoside analogues.
2014
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/2982568
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