Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/36425
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dc.contributor.authorAmat Tusón, Mercedes-
dc.contributor.authorRamos, Carlos-
dc.contributor.authorPérez Bosch, Maria-
dc.contributor.authorMolins i Grau, Elies-
dc.contributor.authorFlorindo, Pedro-
dc.contributor.authorSantos, Maria M. M.-
dc.contributor.authorBosch Cartes, Joan-
dc.date.accessioned2013-04-30T10:52:01Z-
dc.date.available2014-03-07T23:02:13Z-
dc.date.issued2013-03-07-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/2445/36425-
dc.description.abstractStarting from (S)-tryptophanol, a formal synthesis of ent-rhyncho-phylline and ent-isorhynchophylline, involving stereoselective cyclocondensation, spirocyclization, and alkylation reactions, and the final adjustment of the oxidation level at the oxindole and piperidine moieties, is reported.-
dc.format.extent3 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherRoyal Society of Chemistry-
dc.relation.isformatofVersió postprint del document publicat a: http://dx.doi.org/10.1039/c2cc38540f-
dc.relation.ispartofChemical Communications, 2013, vol. 49, num. 19, p. 1954-1956-
dc.relation.urihttp://dx.doi.org/10.1039/c2cc38540f-
dc.rights(c) Amat Tusón, Mercedes et al., 2013-
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)-
dc.subject.classificationAlcaloides-
dc.subject.classificationSíntesi asimètrica-
dc.subject.classificationEstereoquímica-
dc.subject.otherAlkaloids-
dc.subject.otherAsymmetric synthesis-
dc.subject.otherStereochemistry-
dc.titleEnantioselective formal synthesis of ent-rhynchophylline and ent-isorhynchophyllineeng
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec620577-
dc.date.updated2013-04-29T15:13:30Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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