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Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/43586
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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.identifier.issn0022-3263-
dc.identifier.urihttp://hdl.handle.net/2445/43586-
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.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.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-
dc.identifier.idgrec619737-
dc.date.updated2013-05-17T06:23:40Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid23339655-
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