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dc.contributor.authorBradford, T.
dc.contributor.authorPayne, Alan
dc.contributor.authorWillis, A.
dc.contributor.authorPaddon-Row, M.
dc.contributor.authorSherburn, M.
dc.date.accessioned2017-01-30T10:56:17Z
dc.date.available2017-01-30T10:56:17Z
dc.date.created2012-12-03T07:24:55Z
dc.date.issued2010
dc.identifier.citationBradford, Tanya A. and Payne, Alan D. and Willis, Anthony C. and Paddon-Row, Michael N. and Sherburn, Michael S. 2010. Practical synthesis and reactivity of [3]dendralene. Journal of Organic Chemistry 75 (2): pp. 491-494.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/6896
dc.identifier.doi10.1021/jo9024557
dc.description.abstract

A convenient and high-yielding three-step synthesis of the simplest branched triene, [3]dendralene, has been devised. The synthesis is robust and operationally simple, requiring no chromatography and involving no protecting groups or specialized equipment, allowing the synthesis of the volatile hydrocarbon in pure, solvent free form on a multigram scale. The stability, dimerization when stored neat, and Diets-Alder reactivity of [3]dendralene-including double cycloaddition sequences and catalytic enantio selective variant-are reported.

dc.publisherAmerican Chemical Society
dc.subjectPyrolysis
dc.subjectEquivalent
dc.subjectConjugation
dc.subjectHydrocarbons
dc.subject4-Pentadiene
dc.subjectDiels-Alder Reactions
dc.subjectCationic Oxazaborolidines
dc.subjectDendralene Family
dc.subjectCycloadditions
dc.subject3-Methylene-1
dc.subjectCatalysis
dc.titlePractical synthesis and reactivity of [3]dendralene
dc.typeJournal Article
dcterms.source.volume75
dcterms.source.number2
dcterms.source.startPage491
dcterms.source.endPage494
dcterms.source.issn00223263
dcterms.source.titleJournal of Organic Chemistry
curtin.department
curtin.accessStatusFulltext not available


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