Litcius/Paper detail

Gold-Catalyzed Alkynylative Meyer–Schuster Rearrangement

Somsuvra Banerjee, Shivhar B. Ambegave, Ravindra D. Mule, Beeran Senthilkumar, Nitin T. Patil

2020Organic Letters40 citationsDOI

Abstract

By applying the "interplay" mode, which consolidates two key reactivity modes of gold catalysis, namely π-activation mode and cross-coupling mode, the first alkynylative Meyer-Schuster rearrangement is designed and successfully implemented. The current protocol gives straightforward access to enynones, a highly valuable building block, from easily available propargyl alcohol feedstocks. Control experiments suggest an Au(III) catalyst triggers the Meyer-Schuster rearrangement, whereas monitoring the reaction with ESI-HRMS provided strong evidence in favor of a key alkynylgold(III) intermediate which supports the proposed "interplay" scenario.

Topics & Concepts

ChemistryCatalysisRearrangement reactionStereochemistryMedicinal chemistryCombinatorial chemistryOrganic chemistryCatalytic Alkyne ReactionsCatalytic C–H Functionalization MethodsCyclopropane Reaction Mechanisms