4.7 Article

Anilide Formation from Thioacids and Perfluoroaryl Azides

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 80, 期 9, 页码 4392-4397

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.5b00240

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资金

  1. Royal Institute of Technology
  2. National Institutes of Health [R01GM080295]
  3. National Science Foundation [CHE-1112436]
  4. China Scholarship Council
  5. Direct For Mathematical & Physical Scien
  6. Division Of Chemistry [1112436] Funding Source: National Science Foundation

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A metal-free method for fast and clean anilide formation from perfluoroaryl azide and thioacid is presented. The reaction proved highly efficient, displaying fast kinetics, high yield, and good chemoselectivity. The transformation was compatible with various solvents and tolerant to a wide variety of functional groups, and it showed high performance in polar protic/aprotic media, including aqueous buffer systems.

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