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Total Synthesis of (+/-)-Joubertinamine from 3-(3,4-dimethoxyphenyl)-5-bromo-2-pyrone

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dc.contributor.authorTam, Nguyen Thanh-
dc.contributor.authorCho, Cheon-Gyu-
dc.date.accessioned2022-12-21T07:00:17Z-
dc.date.available2022-12-21T07:00:17Z-
dc.date.created2022-08-26-
dc.date.issued2007-08-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/179794-
dc.description.abstractThe regioselective synthesis and Diels-Alder cycloaddition of 3-(3,4-dimethoxyphenyl)-5-bromo-2-pyrone provided a new efficient synthetic route to joubertinamine (9.6% total yield over 10 steps).-
dc.language영어-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.titleTotal Synthesis of (+/-)-Joubertinamine from 3-(3,4-dimethoxyphenyl)-5-bromo-2-pyrone-
dc.typeArticle-
dc.contributor.affiliatedAuthorCho, Cheon-Gyu-
dc.identifier.doi10.1021/ol071381p-
dc.identifier.scopusid2-s2.0-34548168843-
dc.identifier.wosid000248658800049-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.9, no.17, pp.3391 - 3392-
dc.relation.isPartOfORGANIC LETTERS-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume9-
dc.citation.number17-
dc.citation.startPage3391-
dc.citation.endPage3392-
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.keywordPlusQUATERNARY CARBON CENTER-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusSCELETIUM ALKALOIDS-
dc.subject.keywordPlus(-)-MESEMBRINE-
dc.subject.keywordPlusCYCLOADDITION-
dc.subject.keywordPlusJOUBERTINAMINE-
dc.subject.keywordPlus(+)-MESEMBRINE-
dc.subject.keywordPlus3,5-DIBROMO-2-PYRONE-
dc.subject.keywordPlus(+/-)-MESEMBRINE-
dc.subject.keywordPlusCONSTRUCTION-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/ol071381p-
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