The Effective Preparation of Secondary Amines Bearing a Vinylsilane Functionality via the reaction of Primary Amines with α-chlorine-substituted Allylsilanes Catalysed by CuCl
作者:Makoto Kozuka、Michiharu Mitani
DOI:10.3184/030823407x237795
日期:2007.8
The reaction of α-chlorine-substituted allylsilanes with primary amines was promoted by CuCl to result in the selective formation of secondary amines bearing the vinylsilane functionality by a probable SN2′-allylation keeping the silyl group intact.
α-氯取代的烯丙基硅烷与伯胺的反应由 CuCl 促进,导致选择性形成带有乙烯基硅烷官能团的仲胺,通过可能的 SN2'-烯丙基化保持甲硅烷基完整。