Chiral bis(amino amides) as chiral solvating agents for enantiomeric excess determination of α-hydroxy and arylpropionic acids
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Otros documentos de la autoría: Altava, Belen; Burguete, M. Isabel; Carbó Mestre, Noèlia; Escorihuela, Jorge; Luis, Santiago V.
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http://dx.doi.org/10.1016/j.tetasy.2010.05.010 |
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Título
Chiral bis(amino amides) as chiral solvating agents for enantiomeric excess determination of α-hydroxy and arylpropionic acidsAutoría
Fecha de publicación
2010Editor
ElsevierISSN
9574166Cita bibliográfica
Tetrahedron Asymmetry, 21, 8, p. 982-989Tipo de documento
info:eu-repo/semantics/articleResumen
A family of bis(amino amides) derived from natural amino acids has been synthesized and tested for the NMR enantiodiscrimination, as chiral solvating agents, for enantiomeric excess determination of some carboxylic ... [+]
A family of bis(amino amides) derived from natural amino acids has been synthesized and tested for the NMR enantiodiscrimination, as chiral solvating agents, for enantiomeric excess determination of some carboxylic acids. Those bis(amino amide) receptors contain different structural modifications and the splitting of the signals of the acids, after addition of the corresponding CSAs, depends on those structural variables. The influence of aminoacid side chain and the nature of the aliphatic spacer are important parameters to obtain good chiral discriminations. The results obtained clearly show the chiral recognition abilities of these bis(amino amide) ligands and suggest their advantageous use as chiral solvating agents for carboxylic acids. The binding between bis(amino amides) and carboxylic acids has been studied by ESI-MS, NMR, DSC, and molecular modeling. The data suggest that enantiodiscrimination involves the formation of an ionic pair after proton transfer from the carboxylic substrate to the bis(amino amides). © 2010 Elsevier Ltd. All rights reserved. [-]
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