Radical Carboxyarylation Approach to Lignans. Total Synthesis of (-)-Arctigenin, (-)-Matairesinol, and Related Natural Products

dc.contributor.authorFischer, Joshuaen_AU
dc.contributor.authorReynolds, Aaronen_AU
dc.contributor.authorSharp, Lisaen_AU
dc.contributor.authorSherburn, Michaelen_AU
dc.date.accessioned2015-12-13T22:41:10Z
dc.date.available2015-12-13T22:41:10Z
dc.date.issued2004
dc.date.updated2015-12-11T09:59:58Z
dc.description.abstractTotal syntheses of seven biologically important lignan natural products, including (-)-arctigenin, (-)-matairesinol, and (-)α-conidendrin, by way of a highly stereoselective domino radical sequence is presented. The reported stereochemistry of the natura
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/1885/78392
dc.publisherAmerican Chemical Society
dc.sourceOrganic Letters
dc.subjectKeywords: 7 hydroxyarctigenin; arctigenin; conidendrin; lignan derivative; matairesinol; plant extract; unclassified drug; article; arylation; controlled study; diastereoisomer; drug structure; drug synthesis; nonhuman; stereochemistry; Antineoplastic Agents; Antiv
dc.titleRadical Carboxyarylation Approach to Lignans. Total Synthesis of (-)-Arctigenin, (-)-Matairesinol, and Related Natural Products
dc.typeJournal article
local.bibliographicCitation.issue9
local.bibliographicCitation.lastpage1348
local.bibliographicCitation.startpage1345
local.contributor.affiliationFischer, Joshua, University of Sydney
local.contributor.affiliationReynolds, Aaron, University of Sydney
local.contributor.affiliationSharp, Lisa, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationSherburn, Michael, College of Physical and Mathematical Sciences, ANU
local.contributor.authoremailu4053118@anu.edu.au
local.contributor.authoruidSharp, Lisa, u2526236
local.contributor.authoruidSherburn, Michael, u4053118
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationMigratedxPub7049
local.identifier.citationvolume6
local.identifier.doi10.1021/ol049878b
local.identifier.scopusID2-s2.0-2442630439
local.identifier.uidSubmittedByMigrated
local.type.statusPublished Version

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