Issue 5, 2008

Syntheses of manzacidins: a stage for the demonstration of synthetic methodologies

Abstract

Manzacidins, a family of bromopyrrole alkaloids, have attracted much attention from the synthetic community due to their intriguing structures, bearing chiral tertiary and secondary stereocentres in a 1,3-relationship, and biological activities. In this article, we summarise the approaches for the preparation of manzacidins using novel synthetic methodologies. Organocatalysis and Lewis acid catalysis, as well as transition-metal catalysis, offered efficient ways to access these molecules.

Graphical abstract: Syntheses of manzacidins: a stage for the demonstration of synthetic methodologies

Article information

Article type
Emerging Area
Submitted
17 Oct 2007
Accepted
14 Nov 2007
First published
03 Dec 2007

Org. Biomol. Chem., 2008,6, 829-835

Syntheses of manzacidins: a stage for the demonstration of synthetic methodologies

T. Hashimoto and K. Maruoka, Org. Biomol. Chem., 2008, 6, 829 DOI: 10.1039/B716062C

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.

Social activity

Spotlight

Advertisements