Asymmetric Synthesis of Tetrahydroquinolines via Saegusa-type Oxidative Enamine Catalysis/1,5-Hydride Transfer/Cyclization Sequences
DC Field | Value | Language |
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dc.contributor.author | Suh, Chang Won | - |
dc.contributor.author | Woo, Saet Byeol | - |
dc.contributor.author | Kim, Dae Young | - |
dc.date.accessioned | 2021-08-11T22:47:17Z | - |
dc.date.available | 2021-08-11T22:47:17Z | - |
dc.date.issued | 2014-04 | - |
dc.identifier.issn | 2193-5807 | - |
dc.identifier.issn | 2193-5815 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/12292 | - |
dc.description.abstract | Enantioselective organocatalytic synthesis of tetrahydroquinolines has been achieved via Saegusa-type oxidative enamine catalysis/1,5-hydride transfer/cyclization sequences. The feature of this research is a one-pot transformation of 3-aryl aldehydes into tetrahydroquinolines by using environmentally benign catalytic Saegusa oxidation and highly efficient internal redox reactions. The synthetically useful ring-fused tetrahydroquinoline derivatives were obtained in moderate yields and high levels of enantioselectivity. | - |
dc.format.extent | 4 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Wiley - VCH Verlag GmbH & Co. KG | - |
dc.title | Asymmetric Synthesis of Tetrahydroquinolines via Saegusa-type Oxidative Enamine Catalysis/1,5-Hydride Transfer/Cyclization Sequences | - |
dc.type | Article | - |
dc.publisher.location | 독일 | - |
dc.identifier.doi | 10.1002/ajoc.201400022 | - |
dc.identifier.scopusid | 2-s2.0-84899011239 | - |
dc.identifier.wosid | 000334789100009 | - |
dc.identifier.bibliographicCitation | Asian Journal of Organic Chemistry, v.3, no.4, pp 399 - 402 | - |
dc.citation.title | Asian Journal of Organic Chemistry | - |
dc.citation.volume | 3 | - |
dc.citation.number | 4 | - |
dc.citation.startPage | 399 | - |
dc.citation.endPage | 402 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.subject.keywordPlus | H BOND FUNCTIONALIZATION | - |
dc.subject.keywordPlus | N-BOC-ALDIMINES | - |
dc.subject.keywordPlus | ENANTIOSELECTIVE CONJUGATE ADDITION | - |
dc.subject.keywordPlus | MANNICH-TYPE REACTIONS | - |
dc.subject.keywordPlus | BETA-KETO-ESTERS | - |
dc.subject.keywordPlus | BINAPHTHYL-DERIVED ORGANOCATALYSTS | - |
dc.subject.keywordPlus | DIPHENYLPROLINOL SILYL ETHER | - |
dc.subject.keywordPlus | QUATERNARY AMMONIUM-SALTS | - |
dc.subject.keywordPlus | MICHAEL ADDITION | - |
dc.subject.keywordPlus | ALPHA,BETA-UNSATURATED ALDEHYDES | - |
dc.subject.keywordAuthor | aldehydes | - |
dc.subject.keywordAuthor | 1 | - |
dc.subject.keywordAuthor | 5-hydride transfer | - |
dc.subject.keywordAuthor | oxidative enamine catalysis | - |
dc.subject.keywordAuthor | Saegusa oxidation | - |
dc.subject.keywordAuthor | tetrahydroquinolines | - |
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