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Simple and straightforward synthesis of novel enantiopure ionic liquids via efficient enzymatic resolution of (±)-2-(1H-imidazol-1-yl)cyclohexanol

dc.contributor.authorBusto García, Benjamín Eduardo 
dc.contributor.authorGotor Fernández, Vicente 
dc.contributor.authorRíos Lombardía, Nicolás 
dc.contributor.authorGarcía Verdugo, Eduardo
dc.contributor.authorAlfonso, Ignacio
dc.contributor.authorGarcía-Granda, Santiago 
dc.contributor.authorMenéndez Velázquez, Amador 
dc.contributor.authorBurguete, M. Isabel
dc.contributor.authorLuis, Santiago V.
dc.contributor.authorGotor Santamaría, Vicente Miguel 
dc.date.accessioned2020-05-20T09:05:53Z
dc.date.available2020-05-20T09:05:53Z
dc.date.issued2007
dc.identifier.citationTetrahedron Letters, 48(30), p. 5251-5254 (2007); doi:10.1016/j.tetlet.2007.05.138
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/10651/54886
dc.description.abstractBoth enantiomers of enantiopure imidazolium ionic liquids were synthesized by a simple and straightforward procedure from (R,R)- and (S,S)-2-(1H-imidazol-1-yl)cyclohexanol derivatives obtained via lipase-catalyzed resolution. Structural properties and thermal stability of these compounds have been studied to elucidate their potential applications in asymmetric catalysis.spa
dc.description.sponsorshipFinancial support by MEC (CTQ2005-08016-003,MEC-04-CTQ-04185, MAT2006-01997, and Factoría de Cristalización Consolider Ingenio 2010) and Fundació Caixa Castelló—UJI (P1B2004-13) is acknowledged. I.A. and E.G.-V. (Ramo´n y Cajal), V.G.-F. (Juan de la Cierva Program), and E.B. (FPU) thank MEC for personal funding.spa
dc.format.extentp. 5251-5254spa
dc.language.isoengspa
dc.relation.ispartofTetrahedron Letters, 48spa
dc.rights© 2007 Elsevier Ltd.
dc.titleSimple and straightforward synthesis of novel enantiopure ionic liquids via efficient enzymatic resolution of (±)-2-(1H-imidazol-1-yl)cyclohexanolspa
dc.typejournal articlespa
dc.identifier.doi10.1016/j.tetlet.2007.05.138
dc.relation.projectIDMEC/CTQ2005-08016-003spa
dc.relation.projectIDMEC-04-CTQ-04185
dc.relation.projectIDMAT2006-01997
dc.relation.publisherversionhttps://doi.org/10.1016/j.tetlet.2007.05.138spa


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