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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/34862
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dc.contributor.authorHumphries, M.-
dc.contributor.authorMurphy, J.-
dc.contributor.authorPhillips, A.-
dc.contributor.authorAbell, A.-
dc.date.issued2003-
dc.identifier.citationJournal of Organic Chemistry, 2003; 68(6):2432-2436-
dc.identifier.issn0022-3263-
dc.identifier.issn1520-6904-
dc.identifier.urihttp://hdl.handle.net/2440/34862-
dc.descriptionCopyright © 2003 American Chemical Society-
dc.description.abstractA versatile, stereoselective synthesis of 5-hydroxypiperidinones with substituents at N1, C3, and C6 has been developed. The sequence involves ring-closing metathesis of a diene amide and epoxidation of the resulting alkene, followed by base-mediated elimination, and finally hydrogenation.-
dc.description.statementofresponsibilityMark E. Humphries, James Murphy, Andrew J. Phillips, and Andrew D. Abell-
dc.language.isoen-
dc.publisherAmer Chemical Soc-
dc.source.urihttp://pubs.acs.org/cgi-bin/abstract.cgi/joceah/2003/68/i06/abs/jo0267091.html-
dc.titleSynthesis of functionalized piperidinones-
dc.typeJournal article-
dc.identifier.doi10.1021/jo0267091-
pubs.publication-statusPublished-
dc.identifier.orcidAbell, A. [0000-0002-0604-2629]-
Appears in Collections:Aurora harvest 6
Chemistry publications

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