## 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.
1H NMR Analysis of Isocyclosporin A Prepared in Organic Solvent and in Aqueous Solution
β Scribed by Lolita Arnoldi; Ada Manzocchi; Fulvio Magni; Marina Del Puppo; Marzia Galli Kienle
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 194 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0045-2068
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β¦ Synopsis
Isocyclosporins are isomers of cyclosporins deriving from an N,O-acyl transfer occurring under acidic conditions. For the identification by 1 H NMR of isocyclosporins prepared in organic solvents the signal at 2.3 ppm assigned to three hydrogens of the NHCH 3 group is considered. Results reported here show that the 1 H NMR spectrum of isocyclosporin A prepared in aqueous acidic conditions lacks of the above signal and profoundly differs from that of isocyclosporin A prepared in organic solvents, despite the identity of the primary structures determined on the basis of mass spectrometric analysis.
π SIMILAR VOLUMES
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.
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 Proton NMR measurements were performed and ^1^Hο£Ώ^1^H dipolar interaction energies were measured to delineate the conformation of imipramine in solution. Selfβassociation of imipramine into dimers was observed and a dimerization constant of 121 mol^β1^ was calculated. The motional correl