4.7 Article

One-Pot Synthesis of N-Imidoyl-(1H)-indoles via Palladium-Catalyzed Oxidative Insertion Domino Reaction with Isocyanide and Arylboronic Acid

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JOURNAL OF ORGANIC CHEMISTRY
卷 84, 期 12, 页码 8121-8130

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AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.9b00990

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  1. PAPD
  2. (Priority Academic Program Development of Jiangsu Higher Education Institutions)

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Efficient one-pot synthesis of N-imidoyl-(1H)-indoles has been described, which is achieved by the palladium-catalyzed oxidative insertion of 2-(phenylethynyl)-aniline, arylboronic acid, and isonitrile. This method provides a new way to synthesize N-imidoyl-(1H)-indoles, which has a wide substrate scope, good functional group tolerance, and mild reaction condition.

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