4.6 Article

Transition metal-free N-arylation of secondary amides through iodonium salts as aryne precursors

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 14, Issue 43, Pages 10185-10188

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ob01649a

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Funding

  1. National Science Foundation of China [21502054]
  2. East China Normal University (ECNU)

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By using a diaryliodonium salt as a benzyne precursor, a transition metal-free approach for N-arylation of secondary amides is developed. This novel benzyne precursor, which can be prepared easily by a one step process from an aryl iodide, shows different reactivities with previous benzyne precursors in the N-arylation reaction. Mechanistic studies confirm the involvement of benzyne species (generated in situ from the diaryliodonium salts) as key intermediates.

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