The title compounds have been obtained by 1,3-dipolar cycloadditions of methylene nitrones, 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
Procopio A.;Sindona G.
1996-01-01
Abstract
The title compounds have been obtained by 1,3-dipolar cycloadditions of methylene nitrones, 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.File in questo prodotto:
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