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dc.contributor.authorAumann, Kylee M
dc.contributor.authorHealy, Peter C
dc.contributor.authorCoster, Mark J
dc.date.accessioned2017-05-03T15:16:52Z
dc.date.available2017-05-03T15:16:52Z
dc.date.issued2011
dc.date.modified2012-02-14T05:30:20Z
dc.identifier.issn0040-4039
dc.identifier.doi10.1016/j.tetlet.2010.12.076
dc.identifier.urihttp://hdl.handle.net/10072/42572
dc.description.abstractAttempts to selectively arylate [6,6]-spiroacetal enol ethers at the 2-position delivered unexpected results. Palladium-mediated arylation conditions afforded the double-Heck product, whereas reaction with benzenesulfinic acid resulted in a facile rearrangement into the corresponding 5-phenylsulfonyl-3,4,5,6-tetrahydrochromans, providing access to 5-aryl-3,4,5,6-tetrahydrochroman and hexahydrochroman derivatives.
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.languageEnglish
dc.language.isoeng
dc.publisherElsevier
dc.publisher.placeUnited Kingdom
dc.relation.ispartofstudentpublicationN
dc.relation.ispartofpagefrom1070
dc.relation.ispartofpageto1073
dc.relation.ispartofissue10
dc.relation.ispartofjournalTetrahedron Letters
dc.relation.ispartofvolume52
dc.rights.retentionY
dc.subject.fieldofresearchMedicinal and biomolecular chemistry
dc.subject.fieldofresearchOrganic chemistry
dc.subject.fieldofresearchOrganic chemical synthesis
dc.subject.fieldofresearchcode3404
dc.subject.fieldofresearchcode3405
dc.subject.fieldofresearchcode340503
dc.titleArylation of [6,6]-spiroacetal enol ethers: reactivity and rearrangement
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.date.issued2011
gro.hasfulltextNo Full Text
gro.griffith.authorHealy, Peter C.


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