An exploration of the potential of [4+2] cycloadditions of α-pyrones with indenones for the synthesis of the norditerpenoid tropone, harringtonolide

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dc.contributor.authorMander, Lewis
dc.contributor.authorO'Sullivan, Timothy
dc.date.accessioned2015-12-13T23:14:00Z
dc.date.available2015-12-13T23:14:00Z
dc.date.issued2003
dc.date.updated2015-12-12T08:36:37Z
dc.description.abstractThe Diels-Alder reactions of 5-methoxyindenones with various α-pyrones provide the basis for a new and more efficient approach to the synthesis of the unusual nor-diterpenoid tropone, harringtonolide.
dc.identifier.issn0936-5214
dc.identifier.urihttp://hdl.handle.net/1885/88397
dc.publisherGeorg Thieme Verlag
dc.sourceSynlett
dc.subjectKeywords: 2 pyrone derivative; 5 methoxyindenone; diterpenoid; ether; harringtonolide; indene derivative; indenone; tropone derivative; unclassified drug; article; cycloaddition; Diels Alder reaction; synthesis a-pyrone; Cycloaddition; Ether formation; Indenone; Tropone
dc.titleAn exploration of the potential of [4+2] cycloadditions of α-pyrones with indenones for the synthesis of the norditerpenoid tropone, harringtonolide
dc.typeJournal article
local.bibliographicCitation.issue9
local.bibliographicCitation.lastpage1369
local.bibliographicCitation.startpage1367
local.contributor.affiliationMander, Lewis, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationO'Sullivan, Timothy, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidMander, Lewis, u7500768
local.contributor.authoruidO'Sullivan, Timothy, u9804612
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub18078
local.identifier.scopusID2-s2.0-0038442163
local.type.statusPublished Version

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