A new class of potential antiviral drugs is represented by isoxazolidine nucleosides. The paper reports on the synthesis of protected adenines useful as dipolarophiles in the preparation of analogues of dideoxyadenosine by Id-dipolar cycloaddition processes.

A new class of potential antiviral drugs is represented by isoxazolidine nucleosides. The paper reports on the synthesis of protected adenines useful as dipolarophiles in the preparation of analogues of dideoxyadenosine by Id-dipolar cycloaddition processes.

Synthesis of two 6-N-protected 9-N-vinyladenines as dipolarophiles in the synthesis of modified nucleosides

LEGGIO, Antonella;Giglio G;LIGUORI, Angelo;Napoli A;SICILIANO, Carlo;SINDONA, Giovanni
1996-01-01

Abstract

A new class of potential antiviral drugs is represented by isoxazolidine nucleosides. The paper reports on the synthesis of protected adenines useful as dipolarophiles in the preparation of analogues of dideoxyadenosine by Id-dipolar cycloaddition processes.
1996
A new class of potential antiviral drugs is represented by isoxazolidine nucleosides. The paper reports on the synthesis of protected adenines useful as dipolarophiles in the preparation of analogues of dideoxyadenosine by Id-dipolar cycloaddition processes.
vinyladenine; nuclosides; 1,3-dipolar cycloadditions
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/140820
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