Issue 11, 2023

Dirhodium: carbene transformations and beyond

Abstract

Dirhodiums, which feature lantern- or paddlewheel-like structures, have emerged as a class of useful catalysts in organic synthesis. Among the transformations catalyzed by dirhodiums, the carbene, with diazo, cyclopropene, hydrazone and triazole as the precursors, and nitrene transfer reactions are dominant and have reached remarkable levels of efficiency and selectivity. Additionally, more and more fascinating properties of dirhodium have been explored and discovered in the past few decades, which has accelerated the applications of dirhodium in organic synthesis. In this review, we aim to showcase these advances in dirhodium-catalyzed transformations. The transformations including cycloisomerization, hetero-Diels–Alder (HDA) reactions, ene reactions, arylation, radical oxidation reactions and C–H activation, etc. will be covered. In these reactions, the dirhodiums could not only work as redox-neutral catalysts but also as redox catalysts.

Graphical abstract: Dirhodium: carbene transformations and beyond

Article information

Article type
Review Article
Submitted
19 mar. 2023
Accepted
15 apr. 2023
First published
17 apr. 2023

Org. Chem. Front., 2023,10, 2849-2878

Dirhodium: carbene transformations and beyond

R. Wu, D. Zhu and S. Zhu, Org. Chem. Front., 2023, 10, 2849 DOI: 10.1039/D3QO00400G

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