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Dendralenes branch out: cross-conjugated oligoenes allow the rapid generation of molecular complexity

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dc.contributor.authorHopf, Henningen_AU
dc.contributor.authorSherburn, Michaelen_AU
dc.date.accessioned2015-12-10T22:58:38Z
dc.date.issued2012
dc.date.updated2016-02-24T10:25:05Z
dc.description.abstractTwenty-seven years ago, H. Hopf published the only previous comprehensive review on branched oligoenes that had the title "Dendralenes: A Neglected Family of Hydrocarbons". The dendralenes are no longer neglected. Research into the synthesis, properties,
dc.identifier.issn1433-7851
dc.identifier.urihttp://hdl.handle.net/1885/60944
dc.publisherWiley-VCH Verlag GMBH
dc.sourceAngewandte Chemie International Edition
dc.subjectKeywords: Annulenes; cross-conjugation; cycloadditions; dendralenes; Diels-Alder reaction; Domino reactions; Fundamental properties; Gaining momentum; Molecular complexity; Oligoenes; Synthetic approach; Synthetic transformations; Hydrocarbons; Olefins; Organic com cross-conjugation; cycloadditions; dendralenes; domino reactions; hydrocarbons
dc.titleDendralenes branch out: cross-conjugated oligoenes allow the rapid generation of molecular complexity
dc.typeJournal article
local.bibliographicCitation.issue10
local.bibliographicCitation.lastpage2338
local.bibliographicCitation.startpage2298
local.contributor.affiliationHopf, Henning, Technical University of Braunschweig
local.contributor.affiliationSherburn, Michael, College of Physical and Mathematical Sciences, ANU
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.ariespublicationu4005981xPUB575
local.identifier.citationvolume51
local.identifier.doi10.1002/anie.201102987
local.identifier.scopusID2-s2.0-84857946726
local.identifier.thomsonID000300934700004
local.type.statusPublished Version

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