TMSOTf mediated ‘5/6-<i>endo-dig</i>’ reductive hydroamination for the stereoselective synthesis of pyrrolidine and piperidine derivatives

Abstract

A TMSOTf mediated 5/6-endo-dig reductive hydroamination cascade on internal alkynylamines gave expedient, stereoselective access to pyrrolidine and piperidine derivatives. We also demonstrate that a protecting group on nitrogen has a profound effect on the reactivity as well as diastereoselectivity of the reductive hydroamination cascade.