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

Mander, Lewis; O'Sullivan, Timothy

Description

The 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.contributor.authorMander, Lewis
dc.contributor.authorO'Sullivan, Timothy
dc.date.accessioned2015-12-13T23:14:00Z
dc.date.available2015-12-13T23:14:00Z
dc.identifier.issn0936-5214
dc.identifier.urihttp://hdl.handle.net/1885/88397
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.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.description.notesImported from ARIES
local.description.refereedYes
dc.date.issued2003
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub18078
local.type.statusPublished Version
local.contributor.affiliationMander, Lewis, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationO'Sullivan, Timothy, College of Physical and Mathematical Sciences, ANU
local.bibliographicCitation.issue9
local.bibliographicCitation.startpage1367
local.bibliographicCitation.lastpage1369
dc.date.updated2015-12-12T08:36:37Z
local.identifier.scopusID2-s2.0-0038442163
CollectionsANU Research Publications

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