The title compounds have been obtained by 1,3-dipolar cycloadditions of methylene nitromes, prepared in situ from suitably protected hydroxylamines, to 1-N-vinyl-thymine. The 4'-aza-2',3'-dideoxyerythrofuranoside(4), an analogue of 2',3'-dideoxythymidine, might exhibit antiviral activity.

The title compounds have been obtained by 1,3-dipolar cycloadditions of methylene nitromes, prepared in situ from suitably protected hydroxylamines, to 1-N-vinyl-thymine. The 4'-aza-2',3'-dideoxyerythrofuranoside(4), an analogue of 2',3'-dideoxythymidine, might exhibit antiviral activity.

Synthesis of 4'-aza analogues of 2',3'-dideoxythymidine by 1,3-dipolar cycloadditions of nitrones to 1-N-vinyl-thymine

LEGGIO, Antonella;SICILIANO, Carlo;
1996-01-01

Abstract

The title compounds have been obtained by 1,3-dipolar cycloadditions of methylene nitromes, prepared in situ from suitably protected hydroxylamines, to 1-N-vinyl-thymine. The 4'-aza-2',3'-dideoxyerythrofuranoside(4), an analogue of 2',3'-dideoxythymidine, might exhibit antiviral activity.
1996
The title compounds have been obtained by 1,3-dipolar cycloadditions of methylene nitromes, prepared in situ from suitably protected hydroxylamines, to 1-N-vinyl-thymine. The 4'-aza-2',3'-dideoxyerythrofuranoside(4), an analogue of 2',3'-dideoxythymidine, might exhibit antiviral activity.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/126018
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