4.8 Article

Pd(II)-Catalyzed Amination of C-H Bonds Using Single-Electron or Two-electron Oxidants

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 131, Issue 31, Pages 10806-+

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja904709b

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Funding

  1. Scripps Research Institute
  2. U.S. National Science Foundation (NSF) [CHE-0615716]
  3. Pfizer
  4. Camille and Henry Dreyfus Foundation
  5. A. P. Sloan Foundation

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Pd(II)-catalyzed intramolecular amination of arenes is developed using either a one- or two-electron oxidant. The reaction protocol tolerates a wide range of deactivating groups including acetyl, cyano, and nitro groups. This catalytic reaction allows expedient syntheses of broadly useful substituted indolines or indoles.

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