5-Hydroxy-isoxazolidine: A New Synthetic Approach to a Privileged Heterocycle for Organic Synthesis
Articolo
Data di Pubblicazione:
2020
Abstract:
A modified pathway towards 5-hydroxy-isoxazolidines has
been preliminarily investigated by taking advantage of the
anti-Markovnikov route in ene reactions of sterically encumbered
nitrosocarbonyl intermediates in the presence of
allylsilylethers. Fluoride-mediated deprotection/cyclization of
the ene adducts afforded the desired heterocycles in quantitative
yields and the methodology is adaptable to a one-pot
procedure.
been preliminarily investigated by taking advantage of the
anti-Markovnikov route in ene reactions of sterically encumbered
nitrosocarbonyl intermediates in the presence of
allylsilylethers. Fluoride-mediated deprotection/cyclization of
the ene adducts afforded the desired heterocycles in quantitative
yields and the methodology is adaptable to a one-pot
procedure.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Hydroxy-isoxazolidine, nucleosides, heterocyclic, nitrosocarbonyls, silanes
Elenco autori:
Presenti, Piero; Moiola, Mattia; Quadrelli, Paolo
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