Biomimetic total synthesis of (+/-)-berkeleyamide D

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dc.contributor.authorJo, Deokheeko
dc.contributor.authorHan, Sunkyuko
dc.date.accessioned2017-05-15T05:19:53Z-
dc.date.available2017-05-15T05:19:53Z-
dc.date.created2017-03-06-
dc.date.created2017-03-06-
dc.date.created2017-03-06-
dc.date.issued2017-04-
dc.identifier.citationORGANIC CHEMISTRY FRONTIERS, v.4, no.4, pp.506 - 509-
dc.identifier.issn2052-4129-
dc.identifier.urihttp://hdl.handle.net/10203/223699-
dc.description.abstractWe describe the total synthesis of (+/-)-berkeleyamide D using a biosynthetically inspired strategy. The spirocyclic core of berkeleyamide D was constructed via sequential epoxidations and a late-stage base-mediated cyclization of a biosynthetically relevant precursor. Our synthetic solution might be applicable to access other fungal natural products of this family.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleBiomimetic total synthesis of (+/-)-berkeleyamide D-
dc.typeArticle-
dc.identifier.wosid000398911900002-
dc.identifier.scopusid2-s2.0-85016399783-
dc.type.rimsART-
dc.citation.volume4-
dc.citation.issue4-
dc.citation.beginningpage506-
dc.citation.endingpage509-
dc.citation.publicationnameORGANIC CHEMISTRY FRONTIERS-
dc.identifier.doi10.1039/C6QO00812G-
dc.contributor.localauthorHan, Sunkyu-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusASYMMETRIC TOTAL-SYNTHESIS-
dc.subject.keywordPlusPSEUROTIN-A-
dc.subject.keywordPlusABSOLUTE-CONFIGURATION-
dc.subject.keywordPlusANGIOGENESIS INHIBITOR-
dc.subject.keywordPlusASPERGILLUS-FUMIGATUS-
dc.subject.keywordPlusNATURAL-PRODUCTS-
dc.subject.keywordPlusPKS-NRPS-
dc.subject.keywordPlusBIOSYNTHESIS-
dc.subject.keywordPlusAZASPIRENE-
dc.subject.keywordPlusMETABOLITE-
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