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dc.contributor.authorFraile, José M.-
dc.contributor.authorLópez-Ram-de-Víu, Pilar-
dc.contributor.authorMayoral, José A.-
dc.contributor.authorRoldán, Marta-
dc.contributor.authorSantafé-Valero, Jorge-
dc.date.accessioned2012-07-03T08:23:58Z-
dc.date.available2012-07-03T08:23:58Z-
dc.date.issued2011-
dc.identifierdoi: 10.1039/C1OB05499F-
dc.identifierissn: 1477-0520-
dc.identifiere-issn: 1477-0539-
dc.identifier.citationOrganic and Biomolecular Chemistry 9(17): 6075-6081 (2011)-
dc.identifier.urihttp://hdl.handle.net/10261/52672-
dc.description.abstractThe efficiency of chiral bis(oxazoline)- and azabis(oxazoline)-copper complexes in the enantioselective carbene insertion into C-H bonds of cyclic ethers in homogeneous phase strongly depends on the structure of the substrate. The immobilization on laponite clay by electrostatic interactions not only allows the recovery and reuse of the heterogeneous catalysts, but in some cases also improves enantioselectivity and overall chemoselectivity, making possible reactions that do not take place or lead to low yields in solution, even with the commonly used Rh2[S-DOSP]4 catalyst. © 2011 The Royal Society of Chemistry.-
dc.description.sponsorshipFinancial support from the Spanish Ministerio de Ciencia e Innovación (projectsCTQ2008-05138, CTQ2008-00187, andConsolider Ingenio 2010 CSD2006-0003), and theDiputación General de Aragón (E11 Group co-financed by the European Regional Development Funds) is gratefully acknowledged.-
dc.language.isoeng-
dc.publisherRoyal Society of Chemistry (UK)-
dc.rightsopenAccess-
dc.titleEnantioselective C-H carbene insertions with homogeneous and immobilized copper complexes-
dc.typeArtículo-
dc.identifier.doi10.1039/C1OB05499F-
dc.date.updated2012-07-03T08:23:58Z-
dc.description.versionPeer Reviewed-
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