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dc.contributor.authorOlaizola Aizpuru, Olatz
dc.contributor.authorIriarte Arrieta, Igor
dc.contributor.authorZanella, Giovanna
dc.contributor.authorGómez Bengoa, Enrique
dc.contributor.authorGamboa Landa, José Ignacio
dc.contributor.authorOyarbide Garmendia, Juan Miguel
dc.contributor.authorPalomo Nicolau, Claudio
dc.date.accessioned2021-06-29T18:06:21Z
dc.date.available2021-06-29T18:06:21Z
dc.date.issued2019-07-31
dc.identifier.citationAngewandte Chemie International Edition 58(40) : 14250-14254 (2019)es_ES
dc.identifier.issn1433-7851
dc.identifier.urihttp://hdl.handle.net/10810/52087
dc.description.abstractAcatalyst-driven one-pot reaction sequence is developed for the enantio- and diastereoselective synthesis of tetrasubstituted cyclohexenes from simple unsaturated ketones or thioesters.The method involves atertiary amine/squara- mide-catalyzed a-selective addition of transiently generated trienolates to nitroolefins,subsequent base-catalyzed double bond isomerization, and an intramolecular (vinylogous) 1,6- addition reaction, arare key carbocyclization step that proceeded with essentially perfect stereocontroles_ES
dc.description.sponsorshipSupport has been provided by the University of the Basque Country UPV/EHU (UFI QOSYC 11/22), the Basque Government (GV grant No IT-1236-19), and the Ministerio de Economía y Competitividad (MEC Grant CTQ2016-78487-C2), Spain. I.I. and O.O. thank GV for a fellowship. G.Z. and E.G.-B thank the European Funding Horizon 2020-MSCA (ITN-EJD CATMEC 14/06-721223).es_ES
dc.language.isoenges_ES
dc.publisherWiley-VCHes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/721223es_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ2016-78487-C2es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.titleBrønsted Base Catalyzed One-Pot Synthesis od Stereodefined Six-Member Carbocycles Featuring Transient Trienolates and a Key Intramolecular 1,6-Additiones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimes_ES
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/full/10.1002/anie.201908693es_ES
dc.identifier.doidoi.org/10.1002/anie.201908693
dc.identifier.doi10.1002/anie.201908693
dc.contributor.funderEuropean Commission
dc.departamentoesQuímica orgánica Ies_ES
dc.departamentoeuKimika organikoa Ies_ES


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