Issue 13, 2021

C(sp3)–H functionalization with isocyanides

Abstract

Isocyanides are well known for their multi-component reactions (MCR), such as the Passerini reaction and the Ugi reaction, with diverse molecular skeletons, high functional group compatibility, and good atom economy. With the continuous research on isocyanides, C(sp3)–H bond functionalization involving isocyanides has made significant progress in recent years. The synergistic combination of isocyanide insertion and C(sp3)–H bond activation offers an effective strategy for the synthesis of various nitrogen- and oxygen-containing compounds and provides an efficient approach for the synthesis of complex molecules in the fields of synthetic chemistry, drug discovery and materials science. This review highlights the recent progress in the C(sp3)–H functionalization involving isocyanides.

Graphical abstract: C(sp3)–H functionalization with isocyanides

Article information

Article type
Review Article
Submitted
28 яну 2021
Accepted
31 мар 2021
First published
01 апр 2021

Org. Chem. Front., 2021,8, 3525-3542

C(sp3)–H functionalization with isocyanides

W. Wang, T. Liu, C. Ding and B. Xu, Org. Chem. Front., 2021, 8, 3525 DOI: 10.1039/D1QO00153A

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