102590-48-7Relevant academic research and scientific papers
Pd-catalyzed divergent trifluoroethylation and arylation of arylboronic acids by aryl(2,2,2-trifluoroethyl)iodonium triflates
Yang, Jing,Han, Qiu-Yan,Zhao, Cheng-Long,Dong, Tao,Hou, Zhi-Yuan,Qin, Hua-Li,Zhang, Cheng-Pan
, p. 7654 - 7658 (2016)
Highly electrophilic aryl(2,2,2-trifluoroethyl)iodonium triflates have been used for the first time as trifluoroethyl and aryl transfer reagents in Pd-catalyzed functionalization of arylboronic acids. Electron-rich arylboronic acids reacted with aryl(2,2,
Oxidative cross-coupling of arenes induced by single-electron transfer leading to biaryls by use of organoiodine(III)oxidants
Dohi, Toshifumi,Ito, Motoki,Morimoto, Koji,Iwata, Minako,Kita, Yasuyuki
, p. 1301 - 1304 (2008/12/22)
(Chemical Equation Presented) Cross-coupling goes green: The direct oxidative cross-coupling reaction of naphthalenes and other electron-rich arenes with mesitylenes has been achieved in high yields using hypervalent iodine(III) reagents. The key for reac
