Issue 6, 2025

Recent advances in the synthetic applications of nitrosoarene chemistry

Abstract

Nitroso groups are widely present in biologically active compounds in medicinal chemistry, and nitroso compounds serve as important building blocks in organic chemistry and materials science. Nitrosoarenes, in particular, showcase remarkable versatility, functioning as both electrophilic and nucleophilic reagents in a broad spectrum of organic reactions, thereby holding significant relevance in organic chemistry. This review aims to provide a comprehensive overview of the latest advancements in nitrosoarene reactions spanning a decade. Special attention is given to the synthesis of products derived from nitrosoarenes and the conditions that promote these reactions, as well as the type of catalysts. The exploration covers various facets of nitrosoarene chemistry, including cyclization, reactions involving attacks at the oxygen or nitrogen terminus, dimerization, rearrangement, coordination, and other significant reactions. By delving into these diverse reaction pathways and mechanisms, this review aspires to serve as a valuable resource for researchers seeking to deepen their understanding of nitrosoarene chemistry and its applications in both fundamental and applied scientific research.

Graphical abstract: Recent advances in the synthetic applications of nitrosoarene chemistry

Article information

Article type
Review Article
Submitted
14 Oct 2024
Accepted
19 Nov 2024
First published
20 Nov 2024

Org. Biomol. Chem., 2025,23, 1253-1291

Recent advances in the synthetic applications of nitrosoarene chemistry

F. Lin, R. Tang, S. Liu and Y. Tan, Org. Biomol. Chem., 2025, 23, 1253 DOI: 10.1039/D4OB01654H

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