Issue 10, 1990

A short synthesis of prodigiosin analogues

Abstract

A convenient synthetic route to three-ring systems (11) and (12) related to those found in prodigiosin antibiotics is described: the X-ray crystal structure of (12) shows that the exocyclic double bond has a Z-configuration, which allows hydrogen bonding between the methoxy group and the pyrrole NH of ring C.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 734-736

A short synthesis of prodigiosin analogues

A. J. Blake, G. A. Hunter and H. McNab, J. Chem. Soc., Chem. Commun., 1990, 734 DOI: 10.1039/C39900000734

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