4.8 Article

Silver-Mediated Trifluoromethylation-Iodination of Arynes

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 135, Issue 8, Pages 2955-2958

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja312711c

Keywords

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Funding

  1. National Basic Research Program of China [2012CB215500, 2012CB821600]
  2. National Natural Science Foundation of China [20825209, 21102163]
  3. Chinese Academy of Sciences

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An unprecedented silver-mediated vicinal trifluoromethylation-iodination of arynes that quickly introduces CF3 and I groups onto aromatic rings in a single step to give o-trifluoromethyl iodoarenes has been developed. A new reactivity of AgCF3 has been revealed, and 2,2,6,6-tetramethylpiperidine plays an important role in this difunctionalization reaction.

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