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dc.contributor.authorAlcaide, Benito-
dc.contributor.authorAlmendros, Pedro-
dc.date.accessioned2012-07-30T09:53:58Z-
dc.date.available2012-07-30T09:53:58Z-
dc.date.issued2011-
dc.identifierdoi: 10.3762/bjoc.7.73-
dc.identifierissn: 1860-5397-
dc.identifier.citationBeilstein Journal of Organic Chemistry 7: 622- 630 (2011)-
dc.identifier.urihttp://hdl.handle.net/10261/54169-
dc.description.abstractNew gold-catalyzed methods using the β-lactam scaffold have been recently developed for the synthesis of different sized hetero-cycles. This overview focuses on heterocyclization reactions of allenic and alkynic β-lactams which rely on the activation of the allene and alkyne component. The mechanism as well as the regio- and stereoselectivity of the cyclizations are also discussed. © 2011 Alcaide and Almendros.-
dc.language.isoeng-
dc.publisherBeilstein-Institut zur Förderung der Chemischen Wissenschaften-
dc.rightsopenAccess-
dc.titleGold-catalyzed heterocyclizations in alkynyl- and allenyl-β lactams-
dc.typeartículo-
dc.identifier.doihttp://dx.doi.org/10.3762/bjoc.7.73-
dc.date.updated2012-07-30T09:53:59Z-
dc.description.versionPeer Reviewed-
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