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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/101443
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dc.contributor.authorWalker, S.-
dc.contributor.authorCzyz, M.-
dc.contributor.authorMorris, J.-
dc.date.issued2014-
dc.identifier.citationOrganic Letters, 2014; 16(3):708-711-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttp://hdl.handle.net/2440/101443-
dc.description.abstractA synthesis of natural and synthetic members of the meridianin family of kinase inhibitory natural products has been developed. The sequence utilizes a variation of the Cacchi palladium-catalyzed domino reaction to efficiently construct the heterocyclic framework of the meridianins and meriolins from monocyclic precursors.-
dc.description.statementofresponsibilityScott R. Walker, Milena L. Czyz, and Jonathan C. Morris-
dc.language.isoen-
dc.publisherAmerican Chemical Society-
dc.rights© 2014 American Chemical Society-
dc.source.urihttp://dx.doi.org/10.1021/ol403390m-
dc.subjectSyntheses; meridianins; meriolins-
dc.titleConcise syntheses of meridianins and meriolins using a catalytic domino amino-palladation reaction-
dc.typeJournal article-
dc.identifier.doi10.1021/ol403390m-
dc.relation.granthttp://purl.org/au-research/grants/arc/DP0706503-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 7
Chemistry publications

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