The 'H and 13C NMR spectra of amiodarone and several derivatives are reported and assigned. The hypothesis of an 0-trans to 0-cis conformational equilibrium in most of these molecules has been investigated by examining the 'H and I3C chemical shifts, and by NOE and LIS experiments, variable-temperat
1H and 13C NMR analyses of amiodarone, desethylamiodarone and desoxoamiodarone
✍ Scribed by Anthony A. Ribeiro; Gordon L. Jendrasiak
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 879 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The 'H and I3C NMR spectra of amiodarone, a potent cardiac antiarrhythmic agent, desethylamiodarone, the main metabolite of amiodarone and desoxoamiodarone, a less toxic form of amiodarone, were assigned using a combination of NMR techniques. Methods applied include 'H-'H COSY, homonuclear Hartmann-Hahn relayed spectroscopy (HOXAHA), broadband decoupled 'H-"C chemical shift correlation, long-range 'H-I3C chemical shift correlation and selective INEPT. This combination of NMR experiments hss completed a molecular walk along the covalent framework of the cardiac drug molecules, and removed ambiguities in their 'H and 13C NMR assignments.
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