Issue 71, 2025

Transition metal-catalysed asymmetric umpolung reactions of electron-deficient π-unsaturated systems

Abstract

The umpolung reaction of electrophilic π-unsaturated compounds represents a powerful strategy to reverse inherent polarity, enabling unconventional bond formations. While organic σ-Lewis base catalysts are classically utilised, in this feature article, recent advances in the low valent transition metal-mediated asymmetric umpolung reactions of diverse electron-poor unsaturated systems, usually in a diene form, are reviewed, proceeding through either an oxidative cyclometallation or a π-Lewis base activation mechanism. The contents are organised according to transition metal categories, with emphasis on catalytic mechanisms, regio- and stereoselectivity control, and limitations.

Graphical abstract: Transition metal-catalysed asymmetric umpolung reactions of electron-deficient π-unsaturated systems

Article information

Article type
Feature Article
Submitted
26 Jun 2025
Accepted
07 Aug 2025
First published
08 Aug 2025

Chem. Commun., 2025,61, 13378-13388

Transition metal-catalysed asymmetric umpolung reactions of electron-deficient π-unsaturated systems

X. Song, S. Liu, W. Du and Y. Chen, Chem. Commun., 2025, 61, 13378 DOI: 10.1039/D5CC03606B

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