Issue 21, 1974

Methanolysis of flambamycin. Formation and the constitutions of flambalactone, methyl flambate, flambatriose isobutyrate and flambatetrose isobutyrate

Abstract

Mild acidic methanolysis of the antibiotic, flambamycin, yields curacin methyl glycoside (2), flambalactone (35), methyl flambate (39), methyl eurekanate, methyl D-evalopyranoside (10), flambatriose (23), flambatriose isobutyrate (26), flambatetrose (27), and flambatetrose isobutyrate (32).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 882-884

Methanolysis of flambamycin. Formation and the constitutions of flambalactone, methyl flambate, flambatriose isobutyrate and flambatetrose isobutyrate

W. D. Ollis, C. Smith and D. E. Wright, J. Chem. Soc., Chem. Commun., 1974, 882 DOI: 10.1039/C39740000882

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements