Issue 3, 2021

Recent developments in the synthesis of azaindoles from pyridine and pyrrole building blocks

Abstract

The azaindole chemical scaffold is represented in many biologically active natural products and synthetic derivatives. Recently, this chemical scaffold yielded several therapeutic agents for a variety of diseases. Due to the interesting biochemical and biophysical properties of various isomeric azaindoles, numerous investigators have designed and implemented novel synthetic methods for azaindole core units in the past few decades. By using these novel strategies, a number of diversely substituted azaindoles including bioactive natural products, key intermediates and drug candidates have been produced. Herein, we have reviewed the novel synthetic strategies developed for azaindoles since 2011 and highlight their attractive reaction mechanisms, advantages and their limitations. This review may offer potential solutions to develop novel and facile methodologies for the azaindole derivatives of biological interest.

Graphical abstract: Recent developments in the synthesis of azaindoles from pyridine and pyrrole building blocks

Article information

Article type
Review Article
Submitted
04 Sep 2020
Accepted
25 Nov 2020
First published
26 Nov 2020

Org. Chem. Front., 2021,8, 466-513

Recent developments in the synthesis of azaindoles from pyridine and pyrrole building blocks

D. R. Motati, R. Amaradhi and T. Ganesh, Org. Chem. Front., 2021, 8, 466 DOI: 10.1039/D0QO01079K

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