Chemistry of maduramicin I. Salt formation and normal ketalization

13Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

The formation of monovalent and divalent salt complexes of maduramicin is described and the 13C NMR chemical shift assignments of these materials are tabulated and discussed. In the spectrum of the thallium salt, 20 of the 47 signals are split due to the thallium-carbon coupling. Similarly the preparation of both the free acid and the sodium salt complexes of the normal methyl and ethyl ketal derivatives of maduramicin are outlined. Their 13C NMR spectra are fully assigned together with discussion of displacements observed due to this derivatization. © 1986, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.

Cite

CITATION STYLE

APA

Ellestad, G. A., Canfield, N., Leese, R. A., Morton, G. O., James, J. C., Siegel, M. M., & Mcgahren, W. J. (1986). Chemistry of maduramicin I. Salt formation and normal ketalization. The Journal of Antibiotics, 39(3), 447–456. https://doi.org/10.7164/antibiotics.39.447

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free