Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, YS | - |
dc.contributor.author | Kang, SS | - |
dc.contributor.author | Choi, JH | - |
dc.contributor.author | Park, H | - |
dc.date.accessioned | 2024-01-21T18:36:09Z | - |
dc.date.available | 2024-01-21T18:36:09Z | - |
dc.date.created | 2021-09-05 | - |
dc.date.issued | 1997-03 | - |
dc.identifier.issn | 0040-4020 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/143896 | - |
dc.description.abstract | A chiral synthesis of functionalized benzo[a]quinolizine derivative (5) has been accomplished starting from a chiral lactone 7. The key feature is the efficient control of the stereochemistry of ring juncture of the functionalized benzo[a]quinolizine derivative 5 by the N-acyliminium ion cyclization of chiral lactam 11b. (C) 1997 Elsevier Science Ltd. | - |
dc.language | English | - |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
dc.title | Asymmetric synthesis of functionalized benzo[a]quinolizine derivatives via a diastereoselective N-acyliminium ion cyclization | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/S0040-4020(97)00070-7 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | TETRAHEDRON, v.53, no.9, pp.3045 - 3056 | - |
dc.citation.title | TETRAHEDRON | - |
dc.citation.volume | 53 | - |
dc.citation.number | 9 | - |
dc.citation.startPage | 3045 | - |
dc.citation.endPage | 3056 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | A1997WL04000004 | - |
dc.identifier.scopusid | 2-s2.0-0031550875 | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | STEREOSELECTIVE SYNTHESIS | - |
dc.subject.keywordPlus | ENANTIOMERS | - |
dc.subject.keywordPlus | ACID | - |
dc.subject.keywordAuthor | asymmetric | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.