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Thiourea-catalyzed 1,5-hydride transfer and ring closure sequences of o-dialkylamino-substituted nitrostyrenes: Synthesis of ring-fused tetrahydroquinoline derivatives

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posted on 2017-08-21, 18:57 authored by Tae Ho Youn, Dae Young Kim

Thiourea-catalytic synthesis of tetrahydroquinolines has been achieved through a 1,5-hydride transfer/ring closure sequence. The feature of this research is a direct transformation of o-dialkylamino-substituted nitrostyrene derivatives into tetrahydroquinolines using a nitroalkene moiety as hydride acceptor in internal redox reactions.

Funding

This research was supported by Soonchunhyang University Research Fund and Basic Science Research Program through the National Research Foundation of Korea (NRF- 2016R1D1A1B03933723).

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