Total synthesis of (-)-kaitocephalin

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dc.contributor.authorLee, Wonchulko
dc.contributor.authorYoun, Joo-Hackko
dc.contributor.authorKang, SungHoko
dc.date.accessioned2013-08-08T06:06:53Z-
dc.date.available2013-08-08T06:06:53Z-
dc.date.created2013-06-24-
dc.date.created2013-06-24-
dc.date.issued2013-
dc.identifier.citationCHEMICAL COMMUNICATIONS, v.49, no.45, pp.5231 - 5233-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10203/174924-
dc.description.abstract(-)-Kaitocephalin has been synthesized. With the C9 stereocenter from Garner's aldehyde, the C4 quaternary carbon was installed by the desymmetrization of the Cbz-protected serinol. The remaining stereogenic centers were generated through mercuriocyclization, epoxidation and regioselective epoxide opening, in which the quaternary carbon most likely played crucial roles in the stereoinduction.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectRECEPTOR ANTAGONIST-
dc.subjectKAITOCEPHALIN-
dc.subjectALCOHOLS-
dc.subjectREVISION-
dc.subjectACID-
dc.titleTotal synthesis of (-)-kaitocephalin-
dc.typeArticle-
dc.identifier.wosid000318790500035-
dc.identifier.scopusid2-s2.0-84877840225-
dc.type.rimsART-
dc.citation.volume49-
dc.citation.issue45-
dc.citation.beginningpage5231-
dc.citation.endingpage5233-
dc.citation.publicationnameCHEMICAL COMMUNICATIONS-
dc.identifier.doi10.1039/c3cc42365d-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorLee, Wonchul-
dc.contributor.nonIdAuthorYoun, Joo-Hack-
dc.type.journalArticleArticle-
dc.subject.keywordPlusRECEPTOR ANTAGONIST-
dc.subject.keywordPlusKAITOCEPHALIN-
dc.subject.keywordPlusALCOHOLS-
dc.subject.keywordPlusREVISION-
dc.subject.keywordPlusACID-
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