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Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/108109
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dc.contributor.authorAmat Tusón, Mercedes-
dc.contributor.authorBallette, Roberto-
dc.contributor.authorProto, Stefano-
dc.contributor.authorPérez Bosch, Maria-
dc.contributor.authorBosch Cartes, Joan-
dc.date.accessioned2017-03-08T14:53:54Z-
dc.date.available2017-03-08T14:53:54Z-
dc.date.issued2013-03-11-
dc.identifier.issn1359-7345-
dc.identifier.urihttps://hdl.handle.net/2445/108109-
dc.description.abstractThe enantioselective synthesis of advanced tetracyclic precursors of madangamine D, bearing rings ABCD of this alkaloid, is reported. The saturated 14-membered ring is assembled from functionalized diazatricyclic intermediates 10 following either ring-closing metathesis or macrolactamization strategies.-
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/C3CC41104D-
dc.relation.ispartofChemical Communications, 2013, vol. 49, num. 30, p. 3149-3151-
dc.relation.urihttps://doi.org/10.1039/C3CC41104D-
dc.rights(c) Amat Tusón, Mercedes et al., 2013-
dc.sourceArticles publicats en revistes (Nutrició, Ciències de l'Alimentació i Gastronomia)-
dc.subject.classificationAlcaloides-
dc.subject.classificationCompostos heterocíclics-
dc.subject.classificationEstructura molecular-
dc.subject.otherAlkaloids-
dc.subject.otherHeterocyclic compounds-
dc.subject.otherMolecular structure-
dc.titleFirst Enantioselective Synthesis of Tetracyclic Intermediates en route to Madangamine D-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec620999-
dc.date.updated2017-03-08T14:53:54Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
Articles publicats en revistes (Nutrició, Ciències de l'Alimentació i Gastronomia)

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