4.7 Article

Palladium Catalyzed C-I and Vicinal C-H Dual Activation of Diaryliodonium Salts for Diarylations: Synthesis of Triphenylenes

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 83, Issue 1, Pages 49-56

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.7b01905

Keywords

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Funding

  1. National Nature Science Foundation of China [NSFC 21472213, 21272069]
  2. National Key Program [2016YFA0200302]
  3. Fundamental Research Funds for the Central Universities
  4. Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences

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Using the synthetic strategy of palladium catalyzed dual activation of both C-I and vicinal C-H bonds of diaryliodonium salts, we report an approach for direct diarylations of 2-bromobiphenyls or bromobenzenes. As a result, a wide range of triphenylenes with various substituents have been synthesized in good yields. These triphenylenes are expected to be employed in the bottom -up synthesis of functional aromatic molecules in material science.

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