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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/66396
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dc.contributor.authorJeffery, D.-
dc.contributor.authorPerkins, M.-
dc.contributor.authorWhite, J.-
dc.date.issued2005-
dc.identifier.citationOrganic Letters, 2005; 7(8):1581-1584-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttp://hdl.handle.net/2440/66396-
dc.description.abstract[reaction: see text] A short total synthesis of the putative structure of the marine natural product tridachiahydropyrone as a single enantiomer is described. Novel steps include a cuprate addition and cyclization to form a cyclohexanone ring and formation of the bicyclic pyrone with P(2)O(5) on Celite. The spectroscopic data obtained for compound 1 do not match those reported for tridachiahydropyrone; therefore, revision of the assigned natural product structure is warranted.-
dc.description.statementofresponsibilityDavid W. Jeffery, Michael V. Perkins, and Jonathan M. White-
dc.language.isoen-
dc.publisherAmer Chemical Soc-
dc.rightsCopyright © 2005 American Chemical Society-
dc.source.urihttp://dx.doi.org/10.1021/ol050236d-
dc.subjectAnimals-
dc.subjectMollusca-
dc.subjectPyrones-
dc.subjectNuclear Magnetic Resonance, Biomolecular-
dc.subjectMolecular Structure-
dc.subjectCyclization-
dc.subjectStereoisomerism-
dc.titleSynthesis of the putative structure of tridachiahydropyrone-
dc.typeJournal article-
dc.identifier.doi10.1021/ol050236d-
pubs.publication-statusPublished-
dc.identifier.orcidJeffery, D. [0000-0002-7054-0374]-
Appears in Collections:Aurora harvest
Wine Science publications

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