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dc.contributor.authorLee, YS-
dc.contributor.authorMin, BJ-
dc.contributor.authorPark, YK-
dc.contributor.authorLee, JY-
dc.contributor.authorLee, SJ-
dc.contributor.authorPark, H-
dc.date.accessioned2024-01-21T15:12:03Z-
dc.date.available2024-01-21T15:12:03Z-
dc.date.created2021-09-05-
dc.date.issued1999-07-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/142046-
dc.description.abstractThe synthesis of pyrrolidine or piperidine ring-fused 2-phenylazepino[5,4,3-cd]indole derivatives (2) has been accomplished through the N-acyliminium ion cyclization of hydroxy- or alkoxylactams (5) derived from cyclic anhydrides or chiral hydroxy acids. (C) 1999 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleSynthesis of pyrrolidine or piperidine ring-fused azepino[5,4,3-cd]indole derivatives-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4039(99)01076-X-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.40, no.30, pp.5569 - 5572-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume40-
dc.citation.number30-
dc.citation.startPage5569-
dc.citation.endPage5572-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000081427400034-
dc.identifier.scopusid2-s2.0-0033165951-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusACYLIMINIUM ION CYCLIZATION-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusCLAVICIPITIC ACID-
dc.subject.keywordPlusMETHYL-ESTER-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusENANTIOMERS-
dc.subject.keywordPlusINDOLES-
dc.subject.keywordAuthorpyrrolidine-
dc.subject.keywordAuthorSynthesis of pyrrolidine or piperidine ring-fused-
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