articleJournal of the American Chemical SocietyJun 27, 2006Closed access

Intermolecular Amidation of Unactivated sp 2 and sp 3 C−H Bonds via Palladium-Catalyzed Cascade C−H Activation/Nitrene Insertion

State Key Laboratory of Synthetic Chemistry · University of Hong Kong

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Abstract

This communication describes the Pd(OAc)2-catalyzed intermolecular amidation reactions of unactivated sp2 and sp3 C-H bonds using primary amides and potassium persulfate. The substrates containing a pendent oxime or pyridine group were amidated with excellent chemo- and regioselectivities. It is noteworthy that reactive C-X bonds were well-tolerated and a variety of primary amides can be effective nucleophiles for the Pd-catalyzed C-H amidation reactions. For the reaction of unactivated sp3 C-H bonds, beta-amidation of 1 degrees sp3 C-H bonds versus 2 degrees C-H bonds is preferred. The catalytic reaction is initiated by chelation-assisted cyclopalladation involving C-H bond activation. Preliminary mechanistic…

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