4.8 Article

Catalytic C-H Imidation of Aromatic Cores of Functional Molecules: Ligand-Accelerated Cu Catalysis and Application to Materials- and Biology-Oriented Aromatics

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 137, 期 7, 页码 2460-2463

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AMER CHEMICAL SOC
DOI: 10.1021/ja5130012

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  1. ERATO program from JST
  2. JSPS [26888007]
  3. World Premier International Research Center (WPI) Initiative, Japan
  4. Grants-in-Aid for Scientific Research [26888007] Funding Source: KAKEN

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Versatile imidation of aromatic C-H bonds was accomplished. In the presence of copper bromide and 6,6'-dimethyl-2,2'-bipyridyl, a range of aromatics, such as polycyclic aromatic hydrocarbons, aromatic bowls, porphyrins, heteroaromatics, and natural products, can be imidated by N-fluorobenzenesulfonimide. A dramatic ligand-accelerated copper catalysis and an interesting kinetic profile were uncovered.

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