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Total Syntheses of Ningalins D and G

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dc.contributor.authorKim, Jang-Yeop-
dc.contributor.authorKim, Dong-Hyun-
dc.contributor.authorJeon, Tae-Hong-
dc.contributor.authorKim, Woo-Hyung-
dc.contributor.authorCho, Cheon-Gyu-
dc.date.accessioned2022-07-13T11:35:43Z-
dc.date.available2022-07-13T11:35:43Z-
dc.date.issued2017-09-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/151684-
dc.description.abstractA flexible synthetic strategy for the total syntheses of ningalins D and G is described. The highly effective TMS-OTf/2,6-lutidine-mediated [3,3]-sigmatropic rearrangement of densely loaded dinaphthyl hydrazides and cyclization of the resulting 2,2'-diamino-1,1'-dinaphthyls afforded the key 7H-dibenzo[c,g]carbazole intermediates. Successful conversions to biphenylene quinone methides followed by regioselective brominations completed the total syntheses of the titled marine alkaloids.-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleTotal Syntheses of Ningalins D and G-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acs.orglett.7b02372-
dc.identifier.scopusid2-s2.0-85028753035-
dc.identifier.wosid000409566400070-
dc.identifier.bibliographicCitationOrganic Letters, v.19, no.17, pp 4688 - 4691-
dc.citation.titleOrganic Letters-
dc.citation.volume19-
dc.citation.number17-
dc.citation.startPage4688-
dc.citation.endPage4691-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusFISCHER INDOLE SYNTHESIS-
dc.subject.keywordPlusMETHYL ARENES-
dc.subject.keywordPlusALKALOIDS-
dc.subject.keywordPlusREARRANGEMENT-
dc.subject.keywordPlusHYDRAZIDES-
dc.subject.keywordPlusACID-
dc.subject.keywordPlusBROMINATION-
dc.subject.keywordPlusLAMELLARINS-
dc.subject.keywordPlusCOMBINATION-
dc.subject.keywordPlusIODINATION-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acs.orglett.7b02372-
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