化学
对映选择合成
卤素
催化作用
组合化学
镍
烷基
光催化
光催化
光化学
有机化学
作者
Shanya Lu,Zihao Hu,Dong Wang,Tao Xu
标识
DOI:10.1002/anie.202406064
摘要
With halogen-atom transfer as an effective tool, a novel catalytic enantioselective protocol to generate chiral trifluoromethylated alkynes has been established by a cooperative photoredox and nickel catalysis system, providing a straightforward and modular route to access this type of product in good yields and enantioselectivities. The halogen-atom transfer process is essential for the reaction and this novel strategy offers another promising way to utilize alkyl halides with highly negative reduction potentials. It firstly expands nickel-catalyzed asymmetric reductive cross-couplings of organohalides from the traditional single-electron transfer to halogen-atom transfer.
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