4.8 Article

Pd(II)-Catalyzed Ortho Trifluoromethylation of Arenes and Insights into the Coordination Mode of Acidic Amide Directing Groups

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 134, Issue 29, Pages 11948-11951

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja305259n

Keywords

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Funding

  1. The Scripps Research Institute
  2. U.S. NSF [CHE-1011898]
  3. Novartis
  4. China Scholarship Council
  5. National Natural Science Foundation of China [21002070]
  6. Direct For Mathematical & Physical Scien
  7. Division Of Chemistry [1011898] Funding Source: National Science Foundation

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A Pd(II)-catalyzed trifluoromethylation of ortho C-H bonds with an array of N-arylbenzamides derived from benzoic acids is reported. N-Methylformamide has been identified as a crucial promoter of C-CF3 bond formation from the Pd center. X-ray characterization of the C-H insertion intermediate has revealed a rare coordination mode of acidic amides as directing groups and the origin of their capacity in directing C-H activation.

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