Copper-mediated cross-coupling reactions of N-unsubstituted sulfoximines and aryl halides.

Org Lett

Institute of Organic Chemistry, RWTH Aachen University, Professor-Pirlet-Str. 1, D-52056 Aachen, Germany.

Published: September 2004

[reaction: see text] Copper-mediated cross-coupling reactions of sulfoximines with aryl iodides and aryl bromides provide N-arylated sulfoximines in high yields. The method is complementary to the known palladium-catalyzed N-arylation and allows the preparation of N-arylated sulfoximines, which have previously been inaccessible.

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http://dx.doi.org/10.1021/ol048806hDOI Listing

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