Enantioselective Organocatalytic C-H Bond Functionalization via Tandem 1,5-Hydride Transfer/Ring Closure: Asymmetric Synthesis of Tetrahydroquinolines
Enantioselective Organocatalytic C-H Bond Functionalization via Tandem 1,5-Hydride Transfer/Ring Closure: Asymmetric Synthesis of Tetrahydroquinolines
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DOI:
10.1021/ja103786c
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发表时间:
2010-09-01
影响因子:
15
通讯作者:
Kim, Dae Young
中科院分区:
文献类型:
--
作者:
Kang, Young Ku;Kim, Sun Mi;Kim, Dae Young
The first organocatalytic enantioselective intramolecular 1,5-hydride transfer/ring closure reaction is described. This redox neutral reaction cascade allows for the efficient formation of ring-fused tetrahydroquinolines in high enantioselectivities.