Palladium-Catalyzed Intramolecular Hydroarylation of 2-Bromobenzyl Propargyl Ethers: A New Access to Exocyclic Isochromans

Abstract

An efficient, stereo-and regioselective palladium-catalyzed 6-exo-dig intramolecular hydroarylation of propargyl ethers which provides a concise access to functionalized isochromans in high yields has been developed. A wide range of substrates possessing aromatic, aliphatic and heteroaromatic alkynes can be efficiently transformed into the targeted isochromans. Irrespective of the nature of the substrates, the cyclization follows highly selective stereo-and regiochemistry.