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

Author:
Busto García, Benjamín EduardoUniovi authority; Gotor Fernández, VicenteUniovi authority; Ríos Lombardía, NicolásUniovi authority; García Verdugo, Eduardo; Alfonso, Ignacio; García-Granda, SantiagoUniovi authority; Menéndez Velázquez, AmadorUniovi authority; Burguete, M. Isabel; Luis, Santiago V.; Gotor Santamaría, Vicente MiguelUniovi authority
Publication date:
2007
Publisher version:
https://doi.org/10.1016/j.tetlet.2007.05.138
Citación:
Tetrahedron Letters, 48(30), p. 5251-5254 (2007); doi:10.1016/j.tetlet.2007.05.138
Descripción física:
p. 5251-5254
Abstract:

Both 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.

Both 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.

URI:
http://hdl.handle.net/10651/54886
ISSN:
0040-4039
DOI:
10.1016/j.tetlet.2007.05.138
Patrocinado por:

Financial 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.

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