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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
- Youn, Tae Ho;
- Kim, Dae Young
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11초록
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
- 발행일
- 2017
- 유형
- Article
- 권
- 47
- 호
- 22
- 페이지
- 2109 ~ 2114