Lithiated 2-(1-chloroethyl)-4,4-dimethyl-2-oxazoline 7 adds to electron-poor alkenyl heterocycles to afford substituted cyclopropanes in excellent yields. A route to chiral nonracemic heterosubstituted cyclopropanes, starting from optically active 2-chloromethyl-2-oxazolines, is highlighted as well.

Michael Addition of Chloroalkyloxazolines to Electron poor Alkenes: Synthesis of Heterosubstituted Cyclopropanes

CAPRIATI, Vito;LUISI, Renzo
2003-01-01

Abstract

Lithiated 2-(1-chloroethyl)-4,4-dimethyl-2-oxazoline 7 adds to electron-poor alkenyl heterocycles to afford substituted cyclopropanes in excellent yields. A route to chiral nonracemic heterosubstituted cyclopropanes, starting from optically active 2-chloromethyl-2-oxazolines, is highlighted as well.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11586/133203
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