Catalytic enantioselective synthesis of fluoromethylated stereocenters by asymmetric hydrogenation.
Catalytic enantioselective synthesis of fluoromethylated stereocenters by asymmetric hydrogenation.
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DOI:
10.1039/d2sc02685f
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发表时间:
2022-07-29
期刊:
影响因子:
8.4
通讯作者:
Andersson, Pher G.
中科院分区:
文献类型:
--
作者:
Yang, Jianping;Ponra, Sudipta;Li, Xingzhen;Peters, Bram B. C.;Massaro, Luca;Zhou, Taigang;Andersson, Pher G.
Fluoromethyl groups possess specific steric and electronic properties and serve as a bioisostere of alcohol, thiol, nitro, and other functional groups, which are important in an assortment of molecular recognition processes. Herein we report a catalytic method for the asymmetric synthesis of a variety of enantioenriched products bearing fluoromethylated stereocenters with excellent yields and enantioselectivities. Various N,P-ligands were designed and applied in the hydrogenation of fluoromethylated olefins and vinyl fluorides. Herein, a catalytic asymmetric hydrogenation to synthesize various products bearing fluoromethylated stereocenters has been developed.
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