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Apramycin: Complete ^1^H and ^13^C NMR assignments and study of the solution conformation by ROESY measurements by László Szilágyi; Zita Sz. Puzstahelyi is a Chemistry article available to read on EtoBox.

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## Abstract Complete and self‐consistent assignments have been achieved, through the concerted use of various 2D techniques, for the ^1^H and ^13^C NMR spectra of the free base and protonated forms, respectively, of apramycin (1) in D~2~O solution. It is shown that __J__‐relayed dipolar (or __J/R__) and coherent transfer (HOHAHA) processes in ROESY experiments can hardly be eliminated with spin systems such as that studied here. True ROE cross‐peaks can, nevertheless, be identified by varying the experimental conditions. The solution conformation of 1 has been characterized based on the ROESY data, proton‐proton coupling constants and ^13^C __T__~1~ measurements. The 4‐aminoglucose unit appears to be locked together with the octodiose fragment in a conformation satisfying the requirements of the __exo__‐anomeric effects around the C‐1"OC‐8′ bond; the 2‐deoxystreptamine unit, on the other hand, enjoys more rotational freedom around the respective glycosidic bond. The undistorted chair conformations of all six‐membered rings in 1, and the overall conformation of the molecule, are totally independent of the pH, i.e. the protonation state of the molecule.

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Author

László Szilágyi; Zita Sz. Puzstahelyi

Publisher

John Wiley and Sons; Wiley (John Wiley & Sons); John Wiley & Sons Inc.; John Wiley and Sons Ltd; Wiley (ISSN 0749-1581)

Published

1992

Language

EN

Field

Chemistry (Physical Sciences)