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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/17805
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dc.contributor.authorAvery, T.-
dc.contributor.authorCaiazza, D.-
dc.contributor.authorCulbert, J.-
dc.contributor.authorTaylor, D.-
dc.contributor.authorTiekink, E.-
dc.date.issued2005-
dc.identifier.citationJournal of Organic Chemistry, 2005; 70(21):8344-8351-
dc.identifier.issn0022-3263-
dc.identifier.issn1520-6904-
dc.identifier.urihttp://hdl.handle.net/2440/17805-
dc.descriptionCopyright © 2005 American Chemical Society-
dc.description.abstractA new method for the construction of tetrahydropyrans derived from readily available 1,2-dioxines containing a tethered hydroxyl moiety is described. The reaction proceeds via a base-catalyzed rearrangement of the 1,2-dioxines to either the isomeric cis or trans -hydroxy enones followed by intramolecular oxa-Michael addition of the tethered hydroxyl group.-
dc.description.statementofresponsibilityThomas D. Avery, Daniela Caiazza, Julie A. Culbert, Dennis K. Taylor, and Edward R. T. Tiekink-
dc.language.isoen-
dc.publisherAmer Chemical Soc-
dc.source.urihttp://dx.doi.org/10.1021/jo050806n-
dc.subjectHydroxyl Radical-
dc.subjectHeterocyclic Compounds, 1-Ring-
dc.subjectPyrans-
dc.subjectAnticholesteremic Agents-
dc.subjectMolecular Structure-
dc.subjectAntimitotic Agents-
dc.title1,2-dioxines containing tethered hydroxyl functionality as convenient precursors for pyran syntheses-
dc.typeJournal article-
dc.identifier.doi10.1021/jo050806n-
pubs.publication-statusPublished-
dc.identifier.orcidAvery, T. [0000-0001-6882-5461]-
dc.identifier.orcidTaylor, D. [0000-0002-3302-4610] [0000-0002-4274-3983] [0000-0003-0633-7424]-
Appears in Collections:Aurora harvest 6
Chemistry publications

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