Issue 4, 2022

Two decades of recent advances of Passerini reactions: synthetic and potential pharmaceutical applications

Abstract

Passerini three-component reactions (P-3CRs) based on isonitriles are impressive synthetic protocols in which a number of starting materials react with each other to provide poly-functionalized compounds in a one-pot process, a so-called “domino” reaction, minimizing the total number of synthesis steps via a combinatorial protocol. Passerini reactions afford target molecules with highly complex chemical structures and versatile functional groups with good diastereoselectivity. In this review, we highlight recent advances made in relation to the Passerini reaction in the last two decades, from 2000 to 2021, including the potential applications of these compounds in the pharmaceutical field and in the synthesis of peptides, natural products, macrocycles, dendrimers, and a range of heterocycles.

Graphical abstract: Two decades of recent advances of Passerini reactions: synthetic and potential pharmaceutical applications

Article information

Article type
Perspective
Submitted
09 août 2021
Accepted
06 déc. 2021
First published
22 déc. 2021

New J. Chem., 2022,46, 1445-1468

Two decades of recent advances of Passerini reactions: synthetic and potential pharmaceutical applications

Y. Wahby, H. Abdel-Hamid and M. S. Ayoup, New J. Chem., 2022, 46, 1445 DOI: 10.1039/D1NJ03832J

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