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An enantioselective double Diels - Alder approach to the tetracyclic framework of colombiasin A

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dc.contributor.authorChaplin, Jason
dc.contributor.authorEdwards, Alison
dc.contributor.authorFlynn, Bernard
dc.date.accessioned2015-12-13T23:14:10Z
dc.date.available2015-12-13T23:14:10Z
dc.date.issued2003
dc.date.updated2015-12-12T08:37:44Z
dc.description.abstractThe complex tetracyclic carbon skeleton of colombiasin A is conveniently accessed through an enantioselective intermolecular Diels-Alder-sulfoxide elimination-intra-molecular Diels-Alder (DA-E-IMDA) sequence.
dc.identifier.issn1477-0520
dc.identifier.urihttp://hdl.handle.net/1885/88483
dc.publisherRoyal Society of Chemistry
dc.sourceOrganic and Biomolecular Chemistry
dc.subjectKeywords: Heating; Reduction; Single crystals; Stereochemistry; Synthesis (chemical); X ray diffraction analysis; Colombiasin A; Monosilylation; Naphthoquinone sulfoxide; Phenylsulfenic acid; Retrosynthetic analysis; Organic compounds; Betulaceae; bridged compound;
dc.titleAn enantioselective double Diels - Alder approach to the tetracyclic framework of colombiasin A
dc.typeJournal article
local.bibliographicCitation.lastpage1844
local.bibliographicCitation.startpage1842
local.contributor.affiliationChaplin, Jason, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationEdwards, Alison, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationFlynn, Bernard, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidChaplin, Jason, u9904184
local.contributor.authoruidEdwards, Alison, u9900186
local.contributor.authoruidFlynn, Bernard, u9515317
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub18184
local.identifier.citationvolume1
local.identifier.doi10.1039/b302522e
local.identifier.scopusID2-s2.0-0038264406
local.type.statusPublished Version

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