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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

Authors
Youn, Tae HoKim, Dae Young
Issue Date
2017
Publisher
Marcel Dekker Inc.
Keywords
1,5-Hydride transfer; C-H activation; nitroalkenes; redox reaction; tetrahydroquinolines
Citation
Synthetic Communications, v.47, no.22, pp 2109 - 2114
Pages
6
Journal Title
Synthetic Communications
Volume
47
Number
22
Start Page
2109
End Page
2114
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/8412
DOI
10.1080/00397911.2017.1365908
ISSN
0039-7911
1532-2432
Abstract
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.
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