Synthesis and NMR Spectral Data of some Esters Related to the Side Chains in Pluramycin Type Antibiotics

Authors

  • Heinz Nadig Institut für Organische Chemie Universität Basel St. Johanns-Ring 19, CH 4056 Basel
  • Urs Séquin Institut für Organische Chemie Universität Basel St. Johanns-Ring 19, CH 4056 Basel

DOI:

https://doi.org/10.2533/chimia.1987.297

Abstract

Simple methyl esters can serve as suitable model compounds in the structural elucidation of the side chains in pluramycin type antibiotics. The 1H-NMR spectra of the model esters are in good agreement with those of the side chains of the corresponding antibiotics with respect to both, chemical shifts and coupling patterns, the former being consistently at lower fields for the natural products.

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Published

1987-09-30

Issue

Vol. 41 No. 9 (1987): Forschung/Research

Section

Articles

License

Copyright (c) 1987 Heinz Nadig

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

How to Cite

[1]
H. Nadig, U. Séquin, Chimia 1987, 41, 297, DOI: 10.2533/chimia.1987.297.