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 language | English |
---|---|
Pages (from-to) | 5626-5630 |
Number of pages | 5 |
Journal | Organic Letters |
Volume | 23 |
Issue number | 15 |
DOIs | |
State | Published - Aug 6 2021 |
Externally published | Yes |
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.
Funders | Funder number |
---|---|
Nanjing Scientific Research Foundation for Returned Scholars | |
National Natural Science Foundation of China | 21704041, 22075135 |
Six Talent Peaks Project in Jiangsu Province | XCL-027 |