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dc.contributor.authorMagolan, Jakob
dc.contributor.authorCoster, Mark J
dc.date.accessioned2017-05-03T15:16:51Z
dc.date.available2017-05-03T15:16:51Z
dc.date.issued2009
dc.identifier.issn0022-3263
dc.identifier.doi10.1021/jo900613u
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.
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.format.extent126713 bytes
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoeng
dc.publisherThe American Chemical Society
dc.publisher.placeUSA
dc.relation.ispartofstudentpublicationN
dc.relation.ispartofpagefrom5083
dc.relation.ispartofpageto5086
dc.relation.ispartofissue14
dc.relation.ispartofjournalJournal of Organic Chemistry
dc.relation.ispartofvolume74
dc.rights.retentionY
dc.subject.fieldofresearchMedicinal and biomolecular chemistry
dc.subject.fieldofresearchOrganic chemistry
dc.subject.fieldofresearchOrganic chemical synthesis
dc.subject.fieldofresearchcode3404
dc.subject.fieldofresearchcode3405
dc.subject.fieldofresearchcode340503
dc.titleTotal Synthesis of (+)-Angelmarin
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.facultyGriffith Sciences, Griffith Institute for Drug Discovery
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.
gro.date.issued2015-07-30T23:08:50Z
gro.hasfulltextFull Text
gro.griffith.authorCoster, Mark J.
gro.griffith.authorMagolan, Jakob


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