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dc.contributor.authorLee, YS-
dc.contributor.authorKang, SS-
dc.contributor.authorChoi, JH-
dc.contributor.authorPark, H-
dc.date.accessioned2024-01-21T18:36:09Z-
dc.date.available2024-01-21T18:36:09Z-
dc.date.created2021-09-05-
dc.date.issued1997-03-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/143896-
dc.description.abstractA 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.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleAsymmetric synthesis of functionalized benzo[a]quinolizine derivatives via a diastereoselective N-acyliminium ion cyclization-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4020(97)00070-7-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON, v.53, no.9, pp.3045 - 3056-
dc.citation.titleTETRAHEDRON-
dc.citation.volume53-
dc.citation.number9-
dc.citation.startPage3045-
dc.citation.endPage3056-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1997WL04000004-
dc.identifier.scopusid2-s2.0-0031550875-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusSTEREOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusENANTIOMERS-
dc.subject.keywordPlusACID-
dc.subject.keywordAuthorasymmetric-
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