Intramolecular cycloadditions of alpha- allyloxycarbonylnitrones: Stereoselective synthesis of 3-amino- 2(5H)furanones
Articolo
Data di Pubblicazione:
2002
Abstract:
Treatment of furoisoxazolidines with NaH leads
to functionalized 3-amino-2(5H)-furanones through a new
rearrangement pattern of the isoxazolidine nucleus. This
process has been usefully exploited for the synthesis of
enantiomerically pure (5R)-3-alkylamino-5-methyl-2(5H)-
furanones.
Tipologia CRIS:
14.a.1 Articolo su rivista
Keywords:
a-Allyloxycarbonylnitrones; 3-Amino-2(5H)furanones
Elenco autori:
Chiacchio, U; Corsaro, A; Iannazzo, Daniela; Piperno, Anna; Procopio, A; Rescifina, A; Romeo, Giovanni; Romeo, Roberto
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