三氟甲基化
化学
催化作用
有机化学
氧化磷酸化
组合化学
三氟甲基
生物化学
烷基
作者
Sheng Wang,Huanfeng Jiang,Chaorong Qi
标识
DOI:10.1002/ajoc.202300638
摘要
Abstract A copper‐catalyzed oxidative trifluoromethylation of aromatic alkenes has been developed successfully, providing access to a variety of valuable α‐trifluoromethyl‐substituted ketones using Togni's reagent as the trifluoromethyl source. The use of affordable copper catalyst and readily available alkenes as the feedstock, broad substrate scope, mild conditions, and operational simplicity are the attractive features of the method. Preliminary mechanistic studies revealed that both dimethyl sulfoxide (DMSO) and air might function as the oxidant for the transformation.
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