Palladium-Catalyzed Intermolecular Aminoacetoxylation of Alkenes and the Influence of PhI(OAc)<sub>2</sub> on Aminopalladation Stereoselectivity
作者:Claudio Martínez、Yichen Wu、Adam B. Weinstein、Shannon S. Stahl、Guosheng Liu、Kilian Muñiz
DOI:10.1021/jo400671q
日期:2013.6.21
A modified protocol has been identified for Pd-catalyzed intermolecular aininoacetoxylation of terminal and internal alkenes that enables the alkene to be used as the limiting reagent. The results prompt a reassessment of the stereochemical course of these reactions. X-ray crystallographic Characterization of two of the products, together with isotopic labeling studies, show that the amidopalladation step switches from a cis-selective process under aerobic conditions to a trans-selective process in the presence of diacetoxyiodobenzene.