J. Am. Chem. Soc., 127 (1), 72 -73, 2005. 10.1021/ja043898r S0002-7863(04)03898-3
Web Release Date: December 15, 2004

Copyright © 2004 American Chemical Society

Palladium-Catalyzed Intramolecular Coupling between Aryl Iodides and Allyl Moieties via Thermal and Microwave-Assisted Conditions

Mark Lautens,* Eiji Tayama, and Christelle Herse

Davenport Research Laboratories, Department of Chemistry, University of Toronto, Toronto, Ontario, Canada M5S 3H6

mlautens@chem.utoronto.ca

Received October 6, 2004

Abstract:

Palladium-catalyzed intramolecular cross-coupling reactions between aryl iodides and allyl moieties were successfully demonstrated in the presence of palladium catalyst, tri-o-tolylphosphine, a tertiary amine, and water. Several kinds of trans-2,4-disubstituted 1,2,3,4-tetrahydroquinolines were synthesized in 73-88% yields with excellent diastereoselectivities. This method was further applied to a large variety of substrates to form five-, six-, and seven-membered carbo- and heterocycles in good yields, regardless of the ring-containing atom, via microwave-assisted conditions.


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