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Furanodendralenes

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dc.contributor.authorFallon, Thomasen_AU
dc.contributor.authorWillis, Anthonyen_AU
dc.contributor.authorPaddon-Row, Michaelen_AU
dc.contributor.authorSherburn, Michaelen_AU
dc.date.accessioned2015-12-10T23:07:45Z
dc.date.issued2014
dc.date.updated2015-12-10T09:01:44Z
dc.description.abstractAn examination of Diels-Alder reactions of furan-containing analogues of dendralenes has revealed complex and fascinating reaction sequences, which chart the inherent site and stereoselectivity of these processes and give rapid access to structures of high molecular complexity.
dc.identifier.issn0022-3263
dc.identifier.urihttp://hdl.handle.net/1885/63001
dc.publisherAmerican Chemical Society
dc.sourceJournal of Organic Chemistry
dc.titleFuranodendralenes
dc.typeJournal article
local.bibliographicCitation.issue7
local.bibliographicCitation.lastpage3193
local.bibliographicCitation.startpage3185
local.contributor.affiliationFallon, Thomas, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationWillis, Anthony, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationPaddon-Row, Michael, University of New South Wales
local.contributor.affiliationSherburn, Michael, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidFallon, Thomas, u4291744
local.contributor.authoruidWillis, Anthony, u8512028
local.contributor.authoruidSherburn, Michael, u4053118
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.ariespublicationu4005981xPUB759
local.identifier.citationvolume79
local.identifier.doi10.1021/jo500458y
local.identifier.scopusID2-s2.0-84898077478
local.identifier.thomsonID000334016500037
local.type.statusPublished Version

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