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Proton and Carbon Chemical Shift Assignment and Solution-State Conformation of the Macrocyclic Ring in the Macrolide Antibiotic Tylosin in Aprotic Solvents

✍ Scribed by Svetlana Simova; Galya Ivanova


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
415 KB
Volume
34
Category
Article
ISSN
0749-1581

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✦ Synopsis


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 to the x-ray structure in aprotic solvents is proposed.