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Cited 2 time in webofscience Cited 2 time in scopus
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Synthesis of [6,6,m]-Tricyclic Compounds via [4+2] Cycloaddition with Au or Cu Catalyst

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dc.contributor.authorKang, Juyeon-
dc.contributor.authorHam, Seunghwan-
dc.contributor.authorSeong, Chaehyeon-
dc.contributor.authorOh, Chang Ho-
dc.date.accessioned2022-07-06T17:41:33Z-
dc.date.available2022-07-06T17:41:33Z-
dc.date.created2021-07-14-
dc.date.issued2021-06-
dc.identifier.issn0936-5214-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/141830-
dc.description.abstractWe synthesized [6,6,6]- and [6,6,7]-tricyclic compounds via intramolecular [4+2] cycloaddition by gold or copper catalysts. Substrates for cyclization were prepared by coupling reactions between eight types of diyne and four types of aromatic moieties. We have successfully synthesized eleven tricyclic compounds.-
dc.language영어-
dc.language.isoen-
dc.publisherGEORG THIEME VERLAG KG-
dc.titleSynthesis of [6,6,m]-Tricyclic Compounds via [4+2] Cycloaddition with Au or Cu Catalyst-
dc.typeArticle-
dc.contributor.affiliatedAuthorOh, Chang Ho-
dc.identifier.doi10.1055/a-1479-6005-
dc.identifier.scopusid2-s2.0-85105006882-
dc.identifier.wosid000642765900001-
dc.identifier.bibliographicCitationSYNLETT, v.32, no.10, pp.1039 - 1043-
dc.relation.isPartOfSYNLETT-
dc.citation.titleSYNLETT-
dc.citation.volume32-
dc.citation.number10-
dc.citation.startPage1039-
dc.citation.endPage1043-
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.keywordPlus1-oxomiltirone-
dc.subject.keywordPlusabietane derivative-
dc.subject.keywordPlusalkyne derivative-
dc.subject.keywordPlusaromatic amine-
dc.subject.keywordPlusarucadiol-
dc.subject.keywordPluschemical compound-
dc.subject.keywordPluscopper-
dc.subject.keywordPlusdendrodevonin A-
dc.subject.keywordPlusgold-
dc.subject.keywordPlusherbaceous agent-
dc.subject.keywordPlusunclassified drug-
dc.subject.keywordPlus[6,6,6] tricyclic compound-
dc.subject.keywordPlus[6,6,7] tricyclic compound-
dc.subject.keywordPlus[6,6,m]tricyclic compound-
dc.subject.keywordPlusalkylation-
dc.subject.keywordPlusArticle-
dc.subject.keywordPlusbenzannulation reaction-
dc.subject.keywordPlusbromination-
dc.subject.keywordPluscatalysis-
dc.subject.keywordPluschemical reaction-
dc.subject.keywordPluscoupling factor-
dc.subject.keywordPluscyclization-
dc.subject.keywordPluscycloaddition-
dc.subject.keywordPlusDendrobium-
dc.subject.keywordPlusdrug structure-
dc.subject.keywordPlusethynylation-
dc.subject.keywordPlushydrogen bond-
dc.subject.keywordPlusmethylation-
dc.subject.keywordPlussynthesis-
dc.subject.keywordAuthorcatalysis-
dc.subject.keywordAuthor[4+2] cycloaddition-
dc.subject.keywordAuthorabietane-
dc.subject.keywordAuthorDendrobium-
dc.subject.keywordAuthor[6,6,m]-cyclic compound-
dc.subject.keywordAuthorcopper-
dc.subject.keywordAuthorgold-
dc.identifier.urlhttps://www.thieme-connect.de/products/ejournals/abstract/10.1055/a-1479-6005-
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