4.7 Article

Visible-Light-Promoted Oxidative Alkylarylation of N-Aryl/Benzoyl Acrylamides Through Direct C-H Bond Functionalization

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 361, Issue 18, Pages 4237-4242

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201900712

Keywords

Photocatalysis; visible light; alkylarylation; nitrogenous heterocycles; C-H functionalization

Funding

  1. National Natural Science Foundation of China [21502086, 41575118]
  2. Natural Science Foundation of Fujian Province [2019J01744]
  3. Outstanding Youth Science Foundation of Fujian Province [2015J06009]
  4. Program for Excellent Talents of Fujian Province

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Radical cascade oxidative alkylarylations of N-aryl/benzoyl acrylamides have been established through visible-light-enabled photocatalysis, furnishing a wide variety of functionalized oxindoles and isoquinolinediones in good-to-excellent yields under the synergistic interactions of an organic fluorophores-type photocatalyst 4CzIPN, trifluoroacetoxyiodobenzene (PIFA), and 1,3,5-trimethoxybenzene with visible light irradiation. The prominent features of this method are the broad substrate scope, excellent functional group tolerance, and mild reaction conditions.

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