Issue 5, 1989

Stereocontrolled synthesis of andrimid and a structural requirement for the activity

Abstract

Total synthesis of an antibiotic Andrimid was accomplished stereospecifically; it was shown that the chiralities at C-3 and C-4 should be R and S, respectively, and the presence of the (4S)-methyl group is important for the activity.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 299-301

Stereocontrolled synthesis of andrimid and a structural requirement for the activity

W. McWhorter, A. Fredenhagen, K. Nakanishi and H. Komura, J. Chem. Soc., Chem. Commun., 1989, 299 DOI: 10.1039/C39890000299

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