Theoretical Study on Copper-Catalyzed S-Arylation of Thiophenols with Aryl Halides: Evidence Supporting the LCu(I)-SPh Active Catalyst and Halogen Atom Transfer Mechanism

2013 ◽  
Vol 32 (17) ◽  
pp. 4944-4951 ◽  
Author(s):  
Song-Lin Zhang ◽  
Hui-Jun Fan
2012 ◽  
Vol 41 (45) ◽  
pp. 13832 ◽  
Author(s):  
Songlin Zhang ◽  
Zhenzhong Zhu ◽  
Yuqiang Ding

Science ◽  
2020 ◽  
Vol 367 (6481) ◽  
pp. 1021-1026 ◽  
Author(s):  
Timothée Constantin ◽  
Margherita Zanini ◽  
Alessio Regni ◽  
Nadeem S. Sheikh ◽  
Fabio Juliá ◽  
...  

Organic halides are important building blocks in synthesis, but their use in (photo)redox chemistry is limited by their low reduction potentials. Halogen-atom transfer remains the most reliable approach to exploit these substrates in radical processes despite its requirement for hazardous reagents and initiators such as tributyltin hydride. In this study, we demonstrate that α-aminoalkyl radicals, easily accessible from simple amines, promote the homolytic activation of carbon-halogen bonds with a reactivity profile mirroring that of classical tin radicals. This strategy conveniently engages alkyl and aryl halides in a wide range of redox transformations to construct sp3-sp3, sp3-sp2, and sp2-sp2 carbon-carbon bonds under mild conditions with high chemoselectivity.


2014 ◽  
Vol 43 (21) ◽  
pp. 7771 ◽  
Author(s):  
Chun Ran Liu ◽  
Ying Ying Qian ◽  
Kin Shing Chan

2016 ◽  
Vol 145 (24) ◽  
pp. 244705 ◽  
Author(s):  
Shuang-Bao Li ◽  
Yun Geng ◽  
Yu-Ai Duan ◽  
Guang-Yan Sun ◽  
Min Zhang ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document