1314581-33-3Relevant academic research and scientific papers
Palladium-Catalyzed Allylation of Polyfluoroarenes with Allylic Pivalates
Jiang, Xinpeng,Liu, Yong,Zhang, Lei,Chen, Jinkang,Cheng, Kang,Yu, Chuanming
, p. 251 - 255 (2017/09/27)
An efficient 1,5-cyclooctadiene-PdCl 2 /dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (XPhos) catalytic system was developed for C-H allylation of polyfluoroarenes with allylic pivalates. The reactions showed excellent functional-group tolerance, good yields, and high regioselectivities. Mechanistic investigations supported a (π-allyl)palladium complex pathway through a directed oxidative addition of the allylic pivalate to palladium, followed by sequential nucleophilic attack by the polyfluorobenzene and reductive elimination. In a gram-scale reaction, a palladium loading of 0.5 mol% was enough to afford the required product in good yield.
Direct palladium-catalyzed intermolecular allylation of highly electron-deficient polyfluoroarenes
Fan, Shilu,Chen, Fei,Zhang, Xingang
supporting information; experimental part, p. 5918 - 5923 (2011/08/02)
A simple operation: The use of readily available PPh3, high reaction efficiency, and good stereo- and regioselectivity provided useful and operationally simple access to polyfluoroarylated derivatives through the title transformation (see schem
