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dc.contributor.authorMagolan, Jakoben_US
dc.contributor.authorCoster, Marken_US
dc.date.accessioned2017-05-03T15:16:51Z
dc.date.available2017-05-03T15:16:51Z
dc.date.issued2009en_US
dc.identifier.issn00223263en_US
dc.identifier.doi10.1021/jo900613uen_US
dc.identifier.urihttp://hdl.handle.net/10072/30553
dc.description.abstractAn efficient 8-step enantioselective total synthesis of (+)-angelmarin, starting from commercially available umbelliferone, has been achieved. Key reactions include olefin cross-metathesis and a Shi epoxidation-cyclization sequence.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_US
dc.format.extent126713 bytes
dc.format.mimetypeapplication/pdf
dc.languageEnglishen_US
dc.language.isoen_US
dc.publisherThe American Chemical Societyen_US
dc.publisher.placeUSAen_US
dc.relation.ispartofstudentpublicationNen_US
dc.relation.ispartofpagefrom5083en_US
dc.relation.ispartofpageto5086en_US
dc.relation.ispartofissue14en_US
dc.relation.ispartofjournalJournal of Organic Chemistryen_US
dc.relation.ispartofvolume74en_US
dc.rights.retentionYen_US
dc.subject.fieldofresearchOrganic Chemical Synthesisen_US
dc.subject.fieldofresearchcode030503en_US
dc.titleTotal Synthesis of (+)-Angelmarinen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.facultyGriffith Sciences, Griffith Institute for Drug Discoveryen_US
gro.rights.copyrightThis document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Organic Chemistry, copyright 2009 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/jo900613u.en_US
gro.date.issued2015-07-30T23:08:50Z
gro.hasfulltextFull Text


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