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dc.contributor.authorRodríguez Ferrer, Patricia
dc.contributor.authorNaharro, Daniel
dc.contributor.authorMaestro Fernández, Alicia 
dc.contributor.authorAndrés García, José María 
dc.contributor.authorPedrosa Sáez, Rafael 
dc.date.accessioned2019-10-09T08:24:27Z
dc.date.available2019-10-09T08:24:27Z
dc.date.issued2019
dc.identifier.citationEuropean Journal of Organic Chemistry 2019, 6539–6549es
dc.identifier.issn1434-193Xes
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/38452
dc.descriptionProducción Científicaes
dc.description.abstractFour novel chiral bifunctional thiosquaramides have been prepared from cyclopentyl dithiosquarates and diamines derived from natural l‐Valine and l‐tert‐Leucine. The novel thiosquaramides have been tested as organocatalyst in the nitro‐Michael addition of 3‐substituted oxindoles to different β‐aryl‐substituted nitroalkenes. The reaction occurred easily in high yields and excellent stereoselectivities, showing that the novel organocatalysts are much more effective than their thioureas and squaramides homologs.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherWilleyes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectQuímica orgánicaes
dc.titleChiral Bifunctional Thiosquaramides as Organocatalysts in the Synthesis of Enantioenriched 3,3-Disubstituted Oxindoleses
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© Wileyes
dc.identifier.doi10.1002/ejoc.201901327es
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201901327es
dc.identifier.publicationtitleEuropean Journal of Organic Chemistryes
dc.peerreviewedSIes
dc.description.projectJunta de Castilla y León (Ref. Project VA115P17)es
dc.description.projectJunta de Castilla y León (Ref. Project VA149G18)es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/submittedVersiones


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