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ZnCl2-mediated stereoselective addition of terminal alkynes to D-(+)-mannofuranosyl nitrones
Authors:Topi? Dana  Aschwanden Patrick  Fässler Roger  Carreira Erick M
Institution:Laboratorium für Organische Chemie, ETH H?nggerberg, CH-8093 Zürich, Switzerland.
Abstract:reaction: see text] An optimized process for the addition of terminal alkynes to chiral nitrones using ZnCl2 and NEt3 in toluene is reported. The new reaction protocol is facile to perform and cost-effective. The resulting optically active propargyl N-hydroxylamines are isolated in good to excellent yield and high diastereoselectivity.
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