Issue 17, 2024

Photoredox/Cu dual catalyzed 1,4-cyanosulfonylation enabled by remote cyano migration

Abstract

A photoredox/Cu dual catalyzed 1,4-cyanosulfonylation of NHPI esters with readily available sodium arylsulfinates has been established under mild conditions, which provides an expedient approach toward a variety of δ-sulfonyl nitriles with good regioselectivity and functional group tolerance. A mechanism involving decarboxylation-triggered remote cyano migration has been proposed.

Graphical abstract: Photoredox/Cu dual catalyzed 1,4-cyanosulfonylation enabled by remote cyano migration

Supplementary files

Article information

Article type
Research Article
Submitted
10 May 2024
Accepted
11 Jul 2024
First published
12 Jul 2024

Org. Chem. Front., 2024,11, 4857-4861

Photoredox/Cu dual catalyzed 1,4-cyanosulfonylation enabled by remote cyano migration

X. Xie, Y. Li, Z. Bo, Y. Zhu and K. Chen, Org. Chem. Front., 2024, 11, 4857 DOI: 10.1039/D4QO00827H

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