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 spectra of spiramycin I in organic and aqueous solutions
β Scribed by Perwaiz Alam; Jill Barber; Richard J. Brennan; Karen Kennedy; M. Hassan H. Tehrani
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 229 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
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.
π 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 clarithromycin (6β__O__βmethylerythromycin A) in CDCl~3~ and buffered D~2~O were carried out. In contrast to erythromycin A, clarithromycin exists as a single isomer, the 9βketone, in aqueous solution.
0 'H-and 'W-NMR data and spectral assignments are reported for fenobam using noise modulated gated, single frequency off resonance, and single frequency selective proton decoupling techniques. Keyphrases 0 Fenobam-'H-and 13C-NMR spectroscopic analysis 0 'H-and 'T-NMR spectroscopy-analysis of fenoba