A Convenient Synthesis of γ–Amino-Ynamides via Additions of Lithiated Ynamides to Aryl Imines. Observation of an Aza-Meyer-Schuster Rearrangement.

摘要

Efforts in developing an expeditious and convenient method for synthesizing γ–amino-ynamides via nucleophilic addition of lithiated ynamides to aryl imines are described. This work also features an aza-variant of a Meyer-Schuster rearrangement of γ–amino-ynamides and the synthetic utility of γ–amino-ynamides in an intramolecular ketenimine-[2 + 2] cycloaddition.