Thiourea-catalyzed 1,5-hydride transfer and ring closure sequences of o-dialkylamino-substituted nitrostyrenes: Synthesis of ring-fused tetrahydroquinoline derivatives
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Youn, Tae Ho | - |
dc.contributor.author | Kim, Dae Young | - |
dc.date.accessioned | 2021-08-11T16:24:23Z | - |
dc.date.available | 2021-08-11T16:24:23Z | - |
dc.date.issued | 2017 | - |
dc.identifier.issn | 0039-7911 | - |
dc.identifier.issn | 1532-2432 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/8412 | - |
dc.description.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. | - |
dc.format.extent | 6 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Marcel Dekker Inc. | - |
dc.title | Thiourea-catalyzed 1,5-hydride transfer and ring closure sequences of o-dialkylamino-substituted nitrostyrenes: Synthesis of ring-fused tetrahydroquinoline derivatives | - |
dc.type | Article | - |
dc.publisher.location | 미국 | - |
dc.identifier.doi | 10.1080/00397911.2017.1365908 | - |
dc.identifier.scopusid | 2-s2.0-85032186337 | - |
dc.identifier.wosid | 000415695500011 | - |
dc.identifier.bibliographicCitation | Synthetic Communications, v.47, no.22, pp 2109 - 2114 | - |
dc.citation.title | Synthetic Communications | - |
dc.citation.volume | 47 | - |
dc.citation.number | 22 | - |
dc.citation.startPage | 2109 | - |
dc.citation.endPage | 2114 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | sci | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.subject.keywordPlus | ASYMMETRIC MICHAEL ADDITION | - |
dc.subject.keywordPlus | H BOND FUNCTIONALIZATION | - |
dc.subject.keywordPlus | ONE-POT SYNTHESIS | - |
dc.subject.keywordPlus | ORGANOCATALYTIC SYNTHESIS | - |
dc.subject.keywordPlus | TERT-AMINOCYCLIZATION | - |
dc.subject.keywordPlus | MIGRATION SEQUENCES | - |
dc.subject.keywordPlus | HYDRIDE TRANSFER | - |
dc.subject.keywordPlus | BETA-KETOACIDS | - |
dc.subject.keywordPlus | TRANSFER/CYCLIZATION | - |
dc.subject.keywordPlus | ACTIVATION | - |
dc.subject.keywordAuthor | 1,5-Hydride transfer | - |
dc.subject.keywordAuthor | C-H activation | - |
dc.subject.keywordAuthor | nitroalkenes | - |
dc.subject.keywordAuthor | redox reaction | - |
dc.subject.keywordAuthor | tetrahydroquinolines | - |
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