First Enantioselective Synthesis of Tetracyclic Intermediates en route to Madangamine D

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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.date.updated2017-03-08T14:53:54Z
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.identifier.idgrec620999
dc.identifier.issn1359-7345
dc.identifier.urihttps://hdl.handle.net/2445/108109
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.rights.accessRightsinfo:eu-repo/semantics/openAccess
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

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