Nitrene transfer reactions catalysed by copper(I) complexes in ionic liquid using chloramine-T

dc.contributor.authorCano Rico, Israel
dc.contributor.authorNicasio Jaramillo, María Carmen
dc.contributor.authorPérez Romero, Pedro José
dc.date.accessioned2023-12-21T11:24:07Z
dc.date.available2023-12-21T11:24:07Z
dc.date.issued2008
dc.description.abstractThe complex [Tpm*,BrCu(NCMe)]BF4 (Tpm*,Br = HC(3,5-Me2-4-Br-pyrazolyl)3) catalyses the aziridination of alkenes and the amidation of cyclic ethers with chloramine-T as the nitrene source and the ionic liquid [bmim]PF6 as the reaction medium (bmim = 1-n-butyl-3-methylimidazolium). High conversions have been obtained over several cycles of catalyst recovery and reuse.es_ES
dc.description.departmentQuímica "Profesor José Carlos Vílchez Martín"
dc.description.sponsorshipWe thank the MEC (Proyecto CTQ2005-00324/BQU) and the Junta de Andalucía (Proyecto P07-FQM-02745) for financial support. IC thanks MEC for a research fellowship.es_ES
dc.identifier.citationCano, I., Nicasio, M. C., & Pérez, P. J. (2009). Nitrene transfer reactions catalysed by copper(I) complexes in ionic liquid using chloramine-T. In Dalton Trans. (Issue 4, pp. 730–734). Royal Society of Chemistry (RSC). https://doi.org/10.1039/b813469ces_ES
dc.identifier.doi10.1039/B813469C
dc.identifier.issn1477-9226
dc.identifier.issn1477-9234 (electrónico)
dc.identifier.urihttps://hdl.handle.net/10272/22780
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistryes_ES
dc.relation.publisherversionhttps://doi.org/10.1039/B813469Ces_ES
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subject.unesco23 Químicaes_ES
dc.titleNitrene transfer reactions catalysed by copper(I) complexes in ionic liquid using chloramine-Tes_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublication2d8b3544-4704-4909-8786-da298010773d
relation.isAuthorOfPublication884dd5d7-9b4a-45ec-9a62-e46136214a8e
relation.isAuthorOfPublicationc6f8222a-d8d2-4736-baa6-4a2330bdf6b6
relation.isAuthorOfPublication.latestForDiscovery2d8b3544-4704-4909-8786-da298010773d

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