Issue 12, 2021

Pyrrole carboxamide introduction in the total synthesis of pyrrole–imidazole alkaloids

Abstract

In this review various strategies for the incorporation of the signature pyrrole carboxamide moiety in the total syntheses of pyrrole–imidazole alkaloids (PIA) are discussed. These so-called oroidin alkaloids have a broad range of biological activities and display interesting skeletal diversity and complexity. These alkaloids are sponge-derived secondary metabolites and thus far more than 200 members of the PIA family have been isolated over the past few decades. Methods range from classical amide bond forming processes to non-traditional bond formation including the de novo synthesis of the pyrrole itself.

Graphical abstract: Pyrrole carboxamide introduction in the total synthesis of pyrrole–imidazole alkaloids

Article information

Article type
Review Article
Submitted
07 Oct 2020
Accepted
01 Feb 2021
First published
08 Mar 2021

Org. Biomol. Chem., 2021,19, 2603-2621

Author version available

Pyrrole carboxamide introduction in the total synthesis of pyrrole–imidazole alkaloids

A. K. Herath and C. J. Lovely, Org. Biomol. Chem., 2021, 19, 2603 DOI: 10.1039/D0OB02052D

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