H and lSC NMR chemical shifts are reported and assigned for 1,4,9,10-and 2,3,9,1 O-anthracenetetrone. In addition, NMR data are given for 2,3-dihydroxy-9, 1 O-anthraquinone, 2.3-dimethoxy-9.10anthraquinone and 1 -hydroxy-2-acetoxy-9,l O-anthraquinone, encountered during the preparation of the anthra
1H and 13C NMR study of the antihypertensive drugs nifedipine, nicardipine and related compounds
✍ Scribed by Martha S. Morales-Ríos; Alejandra De la Cerda Medina; Victor Pérez-Alvarez; Pedro Joseph-Nathan
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 54 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
One-bond and long-range two-dimensional 1 H and 13 C NMR experiments and deuterium-induced 13 C isotope shifts n C(ND) allow the unequivocal assignment of 13 C and 1 H spectra. On this basis, previous assignments of biologically active nifedipine, nicardipine and related compounds have been revised. The nicardipine chloride salt shows at room temperature two diastereoisomeric configurations due to the asymmetry of substitution at the restricted inverting nitrogen on the NMR time-scale.
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