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Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/160425
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dc.contributor.authorBennasar Fèlix, M. Lluïsa-
dc.contributor.authorZulaica Gallego, Ester-
dc.contributor.authorSolé Arjó, Daniel-
dc.contributor.authorAlonso Serrano, Sandra-
dc.date.accessioned2020-05-15T09:12:08Z-
dc.date.available2020-05-15T09:12:08Z-
dc.date.issued2007-01-
dc.identifier.issn0040-4020-
dc.identifier.urihttp://hdl.handle.net/2445/160425-
dc.description.abstractThe azocino[4,3-b]indole system, tricyclic substructure of the indole alkaloids apparicine and ervaticine, is efficiently assembled by ring-closing metathesis of 2-allyl-3-(allylaminomethyl)indoles. The metathesis sites are introduced into the indole nucleus by reductive amination of a 3-formyl derivative with allylamine, followed by a-lithiation with subsequent electrophilic trapping with acrolein.-
dc.format.extent6 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.tet.2006.11.043-
dc.relation.ispartofTetrahedron, 2007, vol. 63, num. 4, p. 861-866-
dc.relation.urihttps://doi.org/10.1016/j.tet.2006.11.043-
dc.rights(c) Elsevier B.V., 2007-
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)-
dc.subject.classificationAlcaloides-
dc.subject.classificationMetàtesi (Química)-
dc.subject.classificationSíntesi orgànica-
dc.subject.otherAlkaloids-
dc.subject.otherMetathesis (Chemistry)-
dc.subject.otherOrganic synthesis-
dc.titleFacile synthesis of azocino[4,3-b]indoles by ring-closing metathesis-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec555923-
dc.date.updated2020-05-15T09:12:08Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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