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An enantioselective total synthesis of the stilbenolignan (-)-aiphanol and the determination of its absolute stereochemistry

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dc.contributor.authorBanwell, Martin
dc.contributor.authorChand, Satish
dc.contributor.authorSavage, G Paul
dc.date.accessioned2015-12-13T22:34:16Z
dc.date.issued2005
dc.date.updated2015-12-11T09:19:32Z
dc.description.abstractThe title natural product (-)-aiphanol has been prepared by total synthesis. A key step involved the asymmetric dihydroxylation of (E)-3,5-dimethoxy-4-(methoxymethoxy)cinnamyl alcohol with the AD-mix-β to give triol (1R,2R)-1-(3′,5′-dimethoxy-4′-me
dc.identifier.issn0957-4166
dc.identifier.urihttp://hdl.handle.net/1885/76045
dc.publisherPergamon-Elsevier Ltd
dc.sourceTetrahedron: Asymmetry
dc.subjectKeywords: aiphanol; stilbene derivative; unclassified drug; article; asymmetric synthesis; chemical analysis; drug synthesis; enantiomer; enantioselectivity; priority journal; stereochemistry; X ray crystallography
dc.titleAn enantioselective total synthesis of the stilbenolignan (-)-aiphanol and the determination of its absolute stereochemistry
dc.typeJournal article
local.bibliographicCitation.issue9
local.bibliographicCitation.lastpage1654
local.bibliographicCitation.startpage1645
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationChand, Satish, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationSavage, G Paul, CSIRO Molecular and Health Technologies
local.contributor.authoruidBanwell, Martin, u9500594
local.contributor.authoruidChand, Satish, u4021364
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub4955
local.identifier.citationvolume16
local.identifier.doi10.1016/j.tetasy.2005.02.035
local.identifier.scopusID2-s2.0-17844397970
local.type.statusPublished Version

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