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Asymmetric Total Syntheses of (-)-Ervatamine and (+)-19,20-Dehydroervatamine via Late-Stage Directed Indolization

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dc.contributor.authorChen, Qinyang-
dc.contributor.authorJeon, Da-Yun-
dc.contributor.authorCho, Cheon-Gyu-
dc.date.accessioned2025-12-22T05:30:39Z-
dc.date.available2025-12-22T05:30:39Z-
dc.date.issued2025-07-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/209980-
dc.description.abstractAsymmetric total syntheses of (-)-ervatamine and (+)-19,20-dehydroervatamine are described. The key is the directed, late-stage implementation of the indole unit, enabled by the strategically installed ketone group in the central cycloheptene ring.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleAsymmetric Total Syntheses of (-)-Ervatamine and (+)-19,20-Dehydroervatamine via Late-Stage Directed Indolization-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acs.orglett.5c01430-
dc.identifier.scopusid2-s2.0-105012417479-
dc.identifier.wosid001528583500001-
dc.identifier.bibliographicCitationOrganic Letters, v.27, no.29, pp 7744 - 7749-
dc.citation.titleOrganic Letters-
dc.citation.volume27-
dc.citation.number29-
dc.citation.startPage7744-
dc.citation.endPage7749-
dc.type.docTypeArticle; Early Access-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusFISCHER INDOLE SYNTHESIS-
dc.subject.keywordPlusSTEREOCONTROLLED SYNTHESIS-
dc.subject.keywordPlusENANTIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusERVATAMIA-ORIENTALIS-
dc.subject.keywordPlusGENERAL STRATEGY-
dc.subject.keywordPlusALKALOIDS-
dc.subject.keywordPlusREARRANGEMENT-
dc.subject.keywordPlusCOMBINATION-
dc.subject.keywordPlusPOTENT-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acs.orglett.5c01430-
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