Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/36346
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dc.contributor.authorAmat Tusón, Mercedes-
dc.contributor.authorPérez Bosch, Maria-
dc.contributor.authorMinaglia, Annamaria Tania-
dc.contributor.authorBosch Cartes, Joan-
dc.date.accessioned2013-04-25T15:32:01Z-
dc.date.available2013-04-25T15:32:01Z-
dc.date.issued2008-06-13-
dc.identifier.issn0022-3263-
dc.identifier.urihttp://hdl.handle.net/2445/36346-
dc.description.abstractA synthetic route to enantiopure cis-2,4-disubstituted and 2,4-bridged piperidines is reported, the key step being a stereoselective conjugate addition of an organocuprate to a phenylglycinol-derived unsaturated lactam bearing a substituent at the 8a-position.-
dc.format.extent4 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Chemical Society-
dc.relation.isformatofVersió postprint del document publicat a: http://dx.doi.org/10.1021/jo801172b-
dc.relation.ispartofJournal of Organic Chemistry, 2008, vol. 73, num. 17, p. 6920-6923-
dc.relation.urihttp://dx.doi.org/10.1021/jo801172b-
dc.rights(c) American Chemical Society , 2008-
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)-
dc.subject.classificationCompostos organometàl·lics-
dc.subject.classificationCoure-
dc.subject.classificationSíntesi orgànica-
dc.subject.classificationLactames-
dc.subject.otherOrganometallic compounds-
dc.subject.otherCopper-
dc.subject.otherSynthetic organic chemistry-
dc.subject.otherLactams-
dc.titleAn enantioselective synthetic route to cis-2,4-disubstituted and 2,4-bridged piperidines-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec559907-
dc.date.updated2013-04-25T15:32:01Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)

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