## Abstract The 270 MHz ^1^H and 22.6 MHz ^13^C NMR spectra of DL‐phosphothreonine in D~2~O have been measured and analysed as a function of pD. The __trans__‐__trans__ conformation of the fragment H‐αC‐αC‐βOP predominates at all pD values. The C‐β—O __gauche__ contribution is notably larger fo
A 13C NMR study of pyridine in the presence of aqueous solutions of carbohydrates
✍ Scribed by Laurance D. Hall; Mansur Yalpani
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 285 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Spin‐lattice relaxation rates of the ^13^C responses of pyridine were measured in the presence of aqueous sucrose and sodium alginate solutions and calcium alginate gels. In each case the results indicated a reduction in the overall tumbling rate of pyridine compared with that in aqueous media due to molecular association with the carbohydrate. Although anisotropic motion about the C‐4:N axis of pyridine was apparent in the sucrose solutions no consistent trends were observed for the alginate samples.
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## Abstract The ^1^H NMR spectrum of chlorpromazine hydrochloride was fully assigned at 400 MHz. Similarly, the ^13^C NMR spectrum was assigned unambiguously using two‐dimensional NMR. Measurements of chemical shift as a function of concentration in D~2~O showed appreciable changes of shift of both
A detailed analysis of the I3C NMR spectra of the 1-N-and 3-N-methyl derivatives of lH-2-(2,4-dimethoxyphenyI)imidazo[4,5-~]pyridine, utilizing long-range couplings and 2D 'H-I3C correlation experiments, has led to an unambiguous assignment of all carbons. Comparison of these definitive assignments
## Abstract The tautomerism of 5(6)‐methoxy‐2‐{[(4‐methoxy‐3,5‐dimethyl‐2‐pyridinyl)methyl] sulfinyl}‐1__H__‐benzimidazole (omeprazole) was determined in solution, __K__~__T__~ = 0.59 in THF at 195 K, in favor of the 6‐methoxy tautomer. The assignment of the signals was made by comparison with its
The 'H and "C NMR spectra of anhydroerythromycin A in methanol-d, and buffered D,O have been fully assigned using a range of one-and two-dimensional N M R techniques.