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Cited 4 time in webofscience Cited 4 time in scopus
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Total Synthesis of 1-Oxomiltirone and Arucadiol

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dc.contributor.authorSeong, Chaehyeon-
dc.contributor.authorKang, Juyeon-
dc.contributor.authorChai, Uiseong-
dc.contributor.authorMac, Dinh Hung-
dc.contributor.authorOh, Chang Ho-
dc.date.accessioned2022-07-07T09:25:05Z-
dc.date.available2022-07-07T09:25:05Z-
dc.date.created2021-05-12-
dc.date.issued2020-12-
dc.identifier.issn0936-5214-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/144215-
dc.description.abstractA practical and efficient approach for the total synthesis of arucadiol and 1-oxomiltirone is reported. The key step which involves an intramolecular [4+2] cycloaddition catalyzed by gold(III) bromide or copper(II) triflate leads to the formation of 6-6-6-fused aromatic abietane core.-
dc.language영어-
dc.language.isoen-
dc.publisherGEORG THIEME VERLAG KG-
dc.titleTotal Synthesis of 1-Oxomiltirone and Arucadiol-
dc.typeArticle-
dc.contributor.affiliatedAuthorOh, Chang Ho-
dc.identifier.doi10.1055/s-0039-1690743-
dc.identifier.scopusid2-s2.0-85096375812-
dc.identifier.wosid000589940800019-
dc.identifier.bibliographicCitationSYNLETT, v.31, no.19, pp.1953 - 1956-
dc.relation.isPartOfSYNLETT-
dc.citation.titleSYNLETT-
dc.citation.volume31-
dc.citation.number19-
dc.citation.startPage1953-
dc.citation.endPage1956-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusABIETANE DITERPENOIDS-
dc.subject.keywordPlusBENZANNULATION-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusACID-
dc.subject.keywordAuthorarucadiol-
dc.subject.keywordAuthor1-oxomiltirone-
dc.subject.keywordAuthor[4+2]-benzannulation-
dc.subject.keywordAuthorgold(III) bromide-
dc.subject.keywordAuthorcopper(II) trifluoromethanesulfonate-
dc.identifier.urlhttps://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0039-1690743-
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