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.
1H and 13C NMR assignment of sodium chenodeoxycholate in aqueous solution. Polarization of bile salts steroid nucleus
✍ Scribed by J. Zakrzewska; M. Okon; D. Vučelić
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 302 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^1^H and ^13^C NMR assignments of sodium chenodeoxycholate in aqueous solution were obtained for three different bile salt concentrations. ^1^H and ^13^C NMR chemical shifts of sodium chenodeoxycholate and deoxycholate show slight concentration dependence due to micelle formation. Opposite trends in chemical shifts changes for α‐ and β‐protons cause polarization of the steroid nucleus.
📜 SIMILAR VOLUMES
The 'H and 13C N M R spectra of anhydroerythromycin A in methanol-d, and buffered D,O have been fully assigned using a range of one-and two-dimensional NM R techniques.
## Abstract Full assignments of the ^1^H and ^13^C NMR spectra of spiramycin l in CDCl~3~ and buffered D~2~O were carried out unambiguously using a range of 1D and 2D NMR methods.
## 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