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Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/108043
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dc.contributor.authorAmat Tusón, Mercedes-
dc.contributor.authorPinto, Alexandre-
dc.contributor.authorGriera Farres, Rosa-
dc.contributor.authorBosch Cartes, Joan-
dc.date.accessioned2017-03-07T14:28:02Z-
dc.date.available2017-03-07T14:28:02Z-
dc.date.issued2013-12-07-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/2445/108043-
dc.description.abstractA concise synthesis of the marine alkaloids ()-lepadins A-C from a phenylglycinol-derived tricyclic lactam is reported. Key steps from the stereochemical standpoint involve stereoselective cyclocondensation, double bond hydrogenation, oxazolidine opening, hydroboration- oxidation, and Horner-Wadsworth-Emmons reactions.-
dc.format.extent3 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherRoyal Society of Chemistry-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1039/C3CC46801A-
dc.relation.ispartofChemical Communications, 2013, vol. 49, num. 94, p. 11032-11034-
dc.relation.urihttps://doi.org/10.1039/C3CC46801A-
dc.rights(c) Amat Tusón, Mercedes et al., 2013-
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)-
dc.subject.classificationAlcaloides-
dc.subject.classificationLactames-
dc.subject.classificationFarmacologia-
dc.subject.otherAlkaloids-
dc.subject.otherLactams-
dc.subject.otherPharmacology-
dc.titleStereoselectivesynthesis of (-)-lepadins A-C-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec634172-
dc.date.updated2017-03-07T14:28:02Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
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