Abstract
Not one but two: The title reaction proceeds through the dual C-H bond cleavage of both aniline and acetonitrile (see scheme). The reaction affords a variety of cyano-bearing indolinones in excellent yield. Mechanistic studies demonstrate that this reaction involves a fast arylation of the olefin and a rate-determining C-H activation of the acetonitrile. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Wu, T., Mu, X., & Liu, G. (2011). Palladium-catalyzed oxidative arylalkylation of activated alkenes: Dual C-H bond cleavage of an arene and acetonitrile. Angewandte Chemie - International Edition, 50(52), 12578–12581. https://doi.org/10.1002/anie.201104575
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