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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초록

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.

키워드

1,5-Hydride transfer; C-H activation; nitroalkenes; redox reaction; tetrahydroquinolines; ASYMMETRIC MICHAEL ADDITION; H BOND FUNCTIONALIZATION; ONE-POT SYNTHESIS; ORGANOCATALYTIC SYNTHESIS; TERT-AMINOCYCLIZATION; MIGRATION SEQUENCES; HYDRIDE TRANSFER; BETA-KETOACIDS; TRANSFER/CYCLIZATION; ACTIVATION
제목
Thiourea-catalyzed 1,5-hydride transfer and ring closure sequences of o-dialkylamino-substituted nitrostyrenes: Synthesis of ring-fused tetrahydroquinoline derivatives
저자
Youn, Tae Ho; Kim, Dae Young
DOI
10.1080/00397911.2017.1365908
발행일
2017
유형
Article
저널명
Synthetic Communications
권
47
호
22
페이지
2109 ~ 2114