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dc.contributor.authorPedrosa Sáez, Rafael 
dc.contributor.authorAndrés García, José María 
dc.date.accessioned2016-12-05T14:12:13Z
dc.date.available2016-12-05T14:12:13Z
dc.date.issued2015
dc.identifier.citationSustainable Catalysis: Without Metals or Other Endangered Elements, Part 1. Editor, Michael North. 2015, Chapter 6, p.120-139es
dc.identifier.isbn978-1-78262-209-3es
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/21453
dc.descriptionProducción Científicaes
dc.description.abstractProlinamides are valuable organocatalysts for enantioselective transformations that occur by activation of the nucleophile by enamine formation. Different substituents can be appended on the nitrogen atom of the carboxamide, which allow for the modulation of the catalytic properties. In that way, the acidity, the hydrogen donor properties, the hydrophobicity, or the chiral environment can be modified, in a few steps, starting from easily available proline.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherRoyal Society of Chemistryes
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectQuímica orgánicaes
dc.titleProlinamides as Asymmetric Organocatalystses
dc.typeinfo:eu-repo/semantics/bookPartes
dc.rights.holder© The Royal Society of Chemistryes
dc.relation.publisherversionhttp://pubs.rsc.org/es
dc.identifier.publicationfirstpage120es
dc.identifier.publicationlastpage139es
dc.identifier.publicationtitleSustainable Catalysis: Without Metals or Other Endangered Elementses
dc.description.projectMinisterio de Economía, Industria y Competitividad (CTQ2014-59870-P)es
dc.description.projectJunta de Castilla y León (programa de apoyo a proyectos de investigación – Ref. VA064U13)es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International


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