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dc.contributor.authorD. Avery, Thomasen_US
dc.contributor.authorCaiazza, Danielaen_US
dc.contributor.authorA. Culbert, Julieen_US
dc.contributor.authorK.Taylor, Dennisen_US
dc.contributor.authorTiekink, Edwarden_US
dc.date.accessioned2017-04-24T08:01:29Z
dc.date.available2017-04-24T08:01:29Z
dc.date.issued2005en_US
dc.date.modified2009-09-25T04:43:05Z
dc.identifier.issn00223263en_US
dc.identifier.doi10.1021/jo050806nen_AU
dc.identifier.urihttp://hdl.handle.net/10072/4917
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.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherThe American Chemical Societyen_US
dc.publisher.placeWashington, D.C.en_US
dc.publisher.urihttp://pubs.acs.org/journal/joceahen_AU
dc.relation.ispartofstudentpublicationNen_AU
dc.relation.ispartofpagefrom8344en_US
dc.relation.ispartofpageto8351en_US
dc.relation.ispartofjournalJournal of Organic Chemistryen_US
dc.relation.ispartofvolume70en_US
dc.rights.retentionNen_AU
dc.subject.fieldofresearchcode250301en_US
dc.title1,2-dioxines containing tethered hydroxyl functionality as convenient precursors for pyran synthesisen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.description.notepublicCopyright 2005 American Chemical Society. Self-archiving of the author-manuscript version is not yet supported by this publisher. Please use the hypertext link to access the journal's website or contact the author for more information. Please refer to the journal for the definitive published version.en_AU
gro.date.issued2005
gro.hasfulltextNo Full Text


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