posted on 2021-12-21, 18:05authored byFei Cheng, Tao Chen, Yin-Qiu Huang, Jia-Wei Li, Chen Zhou, Xiao Xiao, Fen-Er Chen
We
have developed a high-efficiency and practical Cu-catalyzed
cross-coupling to directly construct versatile α-aryl-esters
by utilizing readily available aryl bromides (or chlorides) and malonates.
These gram-scale approaches occur with turnovers of up to 1560 and
are smoothly conducted by the usage of a low catalyst loading, a new
available ligand, and a green solvent. A variety of functional groups
are tolerated, and the application occurs with α-aryl-esters
to access nonsteroidal anti-inflammatory drugs (NSAIDs) on the gram
scale.