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Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/137117
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dc.contributor.authorAre, Celeste-
dc.contributor.authorPérez Bosch, Maria-
dc.contributor.authorBosch Cartes, Joan-
dc.contributor.authorAmat Tusón, Mercedes-
dc.date.accessioned2019-07-12T07:51:31Z-
dc.date.available2020-05-27T05:10:24Z-
dc.date.issued2019-05-27-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/2445/137117-
dc.description.abstractAn enantioselective formal synthesis of the marine alkaloid madangamine A using phenylglycinol-derived lactam 1 as the starting enantiomeric scaffold is reported. The synthesis involves the construction of the C-9 substituted diazatricyclic ABC core and the final closure of D and E rings from the polyunsaturated skipped intermediate 19.-
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/c9cc03690c-
dc.relation.ispartofChemical Communications, 2019-
dc.relation.urihttps://doi.org/10.1039/c9cc03690c-
dc.rights(c) Are, Celeste et al., 2019-
dc.sourceArticles publicats en revistes (Nutrició, Ciències de l'Alimentació i Gastronomia)-
dc.subject.classificationAlcaloides-
dc.subject.classificationLactames-
dc.subject.classificationCompostos heterocíclics-
dc.subject.classificationSíntesi orgànica-
dc.subject.otherAlkaloids-
dc.subject.otherLactams-
dc.subject.otherHeterocyclic compounds-
dc.subject.otherOrganic synthesis-
dc.titleEnantioselective formal synthesis of (+)-madangamine A-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec690329-
dc.date.updated2019-07-12T07:51:32Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid31165795-
Appears in Collections:Articles publicats en revistes (Nutrició, Ciències de l'Alimentació i Gastronomia)
Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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