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

8 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.

FundersFunder number
Nanjing Scientific Research Foundation for Returned Scholars
National Natural Science Foundation of China21704041, 22075135
Six Talent Peaks Project in Jiangsu ProvinceXCL-027

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