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Construction of the azacyclic core of tabernaemontanine-related alkaloids via tandem reformatsky aza-claisen rearrangement

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dc.contributor.authorSuh, Young-Ger-
dc.contributor.authorLim, Changjin-
dc.contributor.authorSim, Jaehoon-
dc.contributor.authorLee, Jae Kyun-
dc.contributor.authorSurh, Young-Joon-
dc.contributor.authorPaek, Seung-Mann-
dc.date.accessioned2021-01-31T09:23:38Z-
dc.date.available2021-01-31T09:23:38Z-
dc.date.created2017-11-15-
dc.date.issued2017-02-
dc.identifier.citationJournal of Organic Chemistry, Vol.82 No.3, pp.1464-1470-
dc.identifier.issn0022-3263-
dc.identifier.other371-
dc.identifier.urihttps://hdl.handle.net/10371/172634-
dc.description.abstractA divergent synthetic methodology for a tabernaemontanine-related alkaloid was developed. The synthetic route features practical improvements in the Pictet-Spengler cyclization for the tetrahydro-fi-carboline intermediate and an unprecedented tandem Reformatsky aza-Claisen rearrangement to create the core carbon skeleton and stereochemistries of tabernaemontanine-related alkaloids.-
dc.language영어-
dc.publisherAmerican Chemical Society-
dc.titleConstruction of the azacyclic core of tabernaemontanine-related alkaloids via tandem reformatsky aza-claisen rearrangement-
dc.typeArticle-
dc.contributor.AlternativeAuthor서영준-
dc.identifier.doi10.1021/acs.joc.6b02648-
dc.citation.journaltitleJournal of Organic Chemistry-
dc.identifier.wosid000394472900018-
dc.identifier.scopusid2-s2.0-85011319815-
dc.citation.endpage1470-
dc.citation.number3-
dc.citation.startpage1464-
dc.citation.volume82-
dc.identifier.sci000394472900018-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorSuh, Young-Ger-
dc.contributor.affiliatedAuthorSurh, Young-Joon-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusENANTIOSPECIFIC TOTAL-SYNTHESIS-
dc.subject.keywordPlusINDOLE ALKALOIDS-
dc.subject.keywordPlusBISINDOLE ALKALOIDS-
dc.subject.keywordPlusTABEMAEMONTANA-
dc.subject.keywordPlusVOBASINE-
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  • College of Pharmacy
  • Department of Pharmacy
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