Total synthesis of (-)-isoavenaciolide

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dc.contributor.authorSantos, David
dc.contributor.authorAriza Piquer, Xavier
dc.contributor.authorGarcía Gómez, Jordi
dc.contributor.authorLloyd-Williams, Paul
dc.contributor.authorMartínez Laporta, Agustín
dc.contributor.authorSánchez Zarzalejo, Carolina
dc.date.accessioned2013-05-21T08:43:47Z
dc.date.available2014-12-31T23:02:04Z
dc.date.issued2013
dc.date.updated2013-05-17T06:23:40Z
dc.description.abstractAn enantioselective approach to (-)-isoavenaciolide was achieved starting from 1- undecyn-3-ol. The synthesis relied upon the preparation of a chiral 4-silyloxy-2-alkenylborane by hydroboration of a protected 2,3-allenol and subsequent stereoselective addition to 2- thiophenecarboxaldehyde
dc.format.extent6 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec619737
dc.identifier.issn0022-3263
dc.identifier.pmid23339655
dc.identifier.urihttps://hdl.handle.net/2445/43586
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.relation.isformatofVersió postprint del document publicat a: http://dx.doi.org/10.1021/jo302598h
dc.relation.ispartofJournal of Organic Chemistry, 2013, vol. 78, num. 4, p. 1519-1524
dc.relation.urihttp://dx.doi.org/10.1021/jo302598h
dc.rights(c) American Chemical Society , 2013
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Química Inorgànica i Orgànica)
dc.subject.classificationBiomolècules
dc.subject.classificationProductes naturals
dc.subject.classificationSíntesi asimètrica
dc.subject.classificationMedicaments antibacterians
dc.subject.classificationFungicides
dc.subject.otherBiomolecules
dc.subject.otherNatural products
dc.subject.otherAsymmetric synthesis
dc.subject.otherAntibacterial agents
dc.subject.otherFungicides
dc.titleTotal synthesis of (-)-isoavenaciolideeng
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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