C-H Bond Functionalization of (Hetero)aryl Bromide Enabled Synthesis of Brominated Biaryl Compounds

  • Kai Hui Liu
  • , Guang Qi Hu
  • , Cai Xia Wang
  • , Fei Fei Sheng
  • , Jing Wen Bai
  • , Jian Guo Gu
  • , Hong Hai Zhang

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Aryl bromide is one of the most important compounds in organic chemistry, because it is widely used as synthetic building blocks enabling quick access to a wide array of bioactive molecules, organic materials, and polymers via the versatile cutting-edge transformations of C-Br bond. Direct C-H bond functionalization of aryl bromide is considered to be an efficient way to prepare functionalized aryl bromides; however, it is rarely explored possibly due to the relatively low reactivity of aryl bromide toward C-H bond activation. We herein report a palladium-catalyzed coupling reaction between aryl iodide and aryl bromide for preparing brominated biaryl compounds via a silver-mediated C-H bond activation pathway.

Original languageEnglish
Pages (from-to)5626-5630
Number of pages5
JournalOrganic Letters
Volume23
Issue number15
DOIs
StatePublished - Aug 6 2021
Externally publishedYes

Funding

We thank the National Natural Science Foundation of China (Grant Numbers 21704041, 22075135), Six Talent Peaks Project in Jiangsu Province (Grant Numbers XCL-027), and Nanjing Scientific Research Foundation for Returned Scholars for support.

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