4.8 Article

Synthesis of Indolines via Pd(II)-Catalyzed Amination of C-H Bonds Using Phl(OAc)2 as the Bystanding Oxidant

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ORGANIC LETTERS
卷 15, 期 12, 页码 3058-3061

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AMER CHEMICAL SOC
DOI: 10.1021/ol401246u

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  1. Scripps Research Institute
  2. U.S. National Science Foundation [NSF CHE-1011898]
  3. Camille and Henry Dreyfus Foundation for a New Faculty Award
  4. A. P. Sloan Foundation
  5. China Scholarship Council for Oustanding Self-Financed Students Abroad Award
  6. Direct For Mathematical & Physical Scien
  7. Division Of Chemistry [1011898] Funding Source: National Science Foundation

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The Pd(II)-catalyzed intramolecular C-H amination of 2-pyridinesulfonyl-protected phenethylamine derivatives has been achieved using Phl(OAc)(2) as a bystanding oxidant, providing access to a variety of substituted indoline derivatives in good yields. The use of the 2-pyridlnesulfonyl protecting group allows for facile deprotection following C-H functionalization.

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