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dc.contributor.authorLouis, Ignace
dc.contributor.authorL. Hungerford, Natasha
dc.contributor.authorJ. Humphries, Edward
dc.contributor.authorD. McLeod, Malcolm
dc.date.accessioned2017-05-03T15:25:31Z
dc.date.available2017-05-03T15:25:31Z
dc.date.issued2006
dc.date.modified2010-01-11T07:54:46Z
dc.identifier.issn15237052
dc.identifier.doi10.1021/ol053092b
dc.identifier.urihttp://hdl.handle.net/10072/28186
dc.description.abstractThe enantioselective total synthesis of (-)-dactylolide is reported. The absolute stereochemistry of the tetrahydropyran was established by catalytic asymmetric Jacobsen hetero-Diels-Alder reaction. The remote C19 stereocenter was introduced by a sequence of chelation-controlled Grignard addition and Ireland-Claisen rearrangement.
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.languageEnglish
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.publisher.placeWashington, DC
dc.relation.ispartofstudentpublicationN
dc.relation.ispartofpagefrom1117
dc.relation.ispartofpageto1120
dc.relation.ispartofissue6
dc.relation.ispartofjournalOrganic Letters
dc.relation.ispartofvolume8
dc.rights.retentionY
dc.subject.fieldofresearchOrganic Chemical Synthesis
dc.subject.fieldofresearchChemical Sciences
dc.subject.fieldofresearchcode030503
dc.subject.fieldofresearchcode03
dc.titleEnantioselective total synthesis of (-)-dactylolide
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.date.issued2006
gro.hasfulltextNo Full Text
gro.griffith.authorHungerford, Natasha L.


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