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dc.contributor.authorNeves García, Tomaz
dc.contributor.authorVélez Blasco, Andrea 
dc.contributor.authorMartínez de Ilarduya Martínez de Ilarduya, Jesús María 
dc.contributor.authorEspinet Rubio, Pablo 
dc.date.accessioned2018-11-14T08:09:16Z
dc.date.available2018-11-14T08:09:16Z
dc.date.issued2018
dc.identifier.citationChemical Communications, 2018,54, 11809-11812es
dc.identifier.issn1359-7345es
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/32631
dc.descriptionProducción Científicaes
dc.description.abstractChiral-diamine catalyzed addition of ZnMe2 to PhC(O)CF2X (in dichloromethane at −30 °C) affords fluorinated alkyl tertiary alcohols in high yield (quantitative for X = H, F, Cl; 84% for X = CF3) and up to 99% ee. These conditions are similarly very efficient for other various ArC(O)CF3 molecules. A fine analysis of the results can be performed based on a double-cycle mechanism.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherRoyal Society of Chemistryes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.classificationQuímica organometálicaes
dc.subject.classificationOrganometallic chemistryes
dc.titleHighly enantioselective addition of dimethylzinc to fluorinated alkyl ketones, and the mechanism behind ites
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2018 Royal Society of Chemistry
dc.identifier.doihttps://doi.org/10.1039/C8CC06358Ces
dc.relation.publisherversionhttps://pubs.rsc.org/en/content/articlelanding/2018/cc/c8cc06358c#!divAbstractes
dc.peerreviewedSIes
dc.description.projectMinisterio de Economía, Industria y Competitividad (Projects CTQ-2016-80913-P and CTQ2014-52796)es
dc.description.projectJunta de Castilla y León (programa de apoyo a proyectos de investigación - Ref. VA051P17)es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersion


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