1H NMR discrimination of CHF4226.01 diastereoisomers in DMSO-d6
Two diastereoisomers CHF4226.01 (R, R) and CHF4232.01 (S, R), differing for a chiral center, have been studied to investigate their possible discrimination using NMR. 1D NMR and 2D NMR experiments, such as COSY, NOESY and ROESY, were performed on pure isomers and on the association complexes formed...
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Veröffentlicht in: | Magnetic resonance in chemistry 2009-07, Vol.47 (7), p.551-561 |
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Sprache: | eng |
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Zusammenfassung: | Two diastereoisomers CHF4226.01 (R, R) and CHF4232.01 (S, R), differing for a chiral center, have been studied to investigate their possible discrimination using NMR. 1D NMR and 2D NMR experiments, such as COSY, NOESY and ROESY, were performed on pure isomers and on the association complexes formed in the presence of the chiral reagent (S)‐(−)‐1‐(2‐napthyl)ethylamine (S‐NEA). Moreover, computational studies, concerning conformational analysis and molecular dynamics, were started and supported the NMR results. Copyright © 2009 John Wiley & Sons, Ltd.
Two diastereoisomers CHF4226.01 (R, R) and CHF4232.01 (S, R), differing for a chiral centre, have been studied to investigate their possible discrimination by using NMR. 1D NMR and 2D NMR experiments, such as COSY, NOESY and roesy, were performed on pure isomers and on the association complexes formed in the presence of the chiral reagent (S)‐(‐)‐1‐(2‐napthyl)ethylamine (S‐NEA). Moreover computational studies, concerning conformational analysis and molecular dynamics, were started and supported the NMR results. |
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ISSN: | 0749-1581 1097-458X |
DOI: | 10.1002/mrc.2427 |