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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/70984
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dc.contributor.authorSpence, J.-
dc.contributor.authorGeorge, J.-
dc.date.issued2011-
dc.identifier.citationOrganic Letters, 2011; 13(19):5318-5321-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttp://hdl.handle.net/2440/70984-
dc.description.abstractA structure revision for the recently isolated fungal meroterpenoids, cytosporolides A-C, is suggested based on biosynthetic speculation and reinterpretation of existing spectroscopic data. The structure revision is supported by a biomimetic synthetic study, featuring a [4 + 2] cycloaddition reaction between a presumed o-quinone methide intermediate and β-caryophyllene.-
dc.description.statementofresponsibilityJustin T. J. Spence and Jonathan H. George-
dc.language.isoen-
dc.publisherAmer Chemical Soc-
dc.rights© 2011 American Chemical Society-
dc.source.urihttp://dx.doi.org/10.1021/ol202181g-
dc.subjectSesquiterpenes-
dc.subjectMagnetic Resonance Spectroscopy-
dc.subjectMolecular Structure-
dc.subjectCyclization-
dc.subjectBiomimetic Materials-
dc.subjectPolycyclic Sesquiterpenes-
dc.titleStructural reassignment of Cytosporolides A - C via biomimetic synthetic studies and reinterpretation of NMR data-
dc.typeJournal article-
dc.identifier.doi10.1021/ol202181g-
pubs.publication-statusPublished-
dc.identifier.orcidGeorge, J. [0000-0002-7330-2160]-
Appears in Collections:Aurora harvest
Chemistry publications

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