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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/122676
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dc.contributor.authorColeman, M.A.-
dc.contributor.authorBurchill, L.-
dc.contributor.authorSumby, C.J.-
dc.contributor.authorGeorge, J.H.-
dc.date.issued2019-
dc.identifier.citationOrganic Letters, 2019; 21(21):8776-8778-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttp://hdl.handle.net/2440/122676-
dc.description.abstractThe structure of furoerioaustralasine, a unique Australian alkaloid, has been revised based on a concise, biomimetic synthesis. The key step is a stereospecific, intramolecular ring opening of an epoxide to form a central dihydrofuran fused to a quinoline ring system.-
dc.description.statementofresponsibilityMatthew A. Coleman, Laura Burchill, Christopher J. Sumby, and Jonathan H. George-
dc.language.isoen-
dc.publisherAmerican Chemical Society-
dc.rights© 2019 American Chemical Society-
dc.source.urihttp://dx.doi.org/10.1021/acs.orglett.9b03392-
dc.subjectAlkaloids-
dc.subjectBiomimetics-
dc.subjectCyclization-
dc.subjectChemistry Techniques, Synthetic-
dc.titleBiomimetic synthesis enables the structure revision of furoerioaustralasine-
dc.typeJournal article-
dc.identifier.doi10.1021/acs.orglett.9b03392-
dc.relation.granthttp://purl.org/au-research/grants/arc/FT170100437-
pubs.publication-statusPublished-
dc.identifier.orcidColeman, M.A. [0000-0003-3813-0815]-
dc.identifier.orcidSumby, C.J. [0000-0002-9713-9599]-
dc.identifier.orcidGeorge, J.H. [0000-0002-7330-2160]-
Appears in Collections:Aurora harvest 4
Chemistry publications

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