Stereoselectivesynthesis of (-)-lepadins A-C

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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.date.updated2017-03-07T14:28:02Z
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.identifier.idgrec634172
dc.identifier.issn1359-7345
dc.identifier.urihttps://hdl.handle.net/2445/108043
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.rights.accessRightsinfo:eu-repo/semantics/openAccess
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

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