The 'H and "C NMR spectra of the 16-membered macrolide antibiotic tylosin were unambiguously assigned. The solution conformation of the macrocyclic ring in aprotic solvents was investigated by a combination of NMR methods and force field calculations. The predominance of the conformer corresponding
Proton and carbon chemical shift assignment and dynamic investigation of the macrolide antibiotic tylosin
β Scribed by Claudio Rossi; Alessandro Donati; Maria Pia Picchi; Maria Rosaria Sansoni; Gianfranco Corbini; Piero Corti
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 271 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
Abstract
The NMR spectral properties of the antibiotic tylosin were investigated. DQβCOSY and HETCOR twoβdimensional spectra were used for the assignment of both the proton and protonated carbon signals. Selective (H)CβNOE, were proposed for the controversial quaternary carbon assignments. The analysis of molecular motion in solution based on carbon spinβlattice relaxation rates shows that tylosin exhibits dynamics that are typical of each molecular moiety. A higher degree of free motion is observed with increasing distance from the macrolide nucleus.
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