Issue 92, 2015

Copper-catalyzed electrophilic amination of sodium sulfinates at room temperature

Abstract

By using O-benzoyl hydroxylamines as amine sources, the first convenient copper-catalyzed electrophilic amination of sodium sulfinates has been realized. Even with 2 mol% catalyst loading, the protocol provided an efficient and straightforward synthesis of a broad range of functional sulfonamides under ambient reaction conditions without an additional base and ligand. Based on the control experiments, a plausible mechanism was proposed.

Graphical abstract: Copper-catalyzed electrophilic amination of sodium sulfinates at room temperature

Supplementary files

Article information

Article type
Communication
Submitted
21 Jul 2015
Accepted
16 Sep 2015
First published
17 Sep 2015

Chem. Commun., 2015,51, 16573-16576

Author version available

Copper-catalyzed electrophilic amination of sodium sulfinates at room temperature

H. Zhu, Y. Shen, Q. Deng and T. Tu, Chem. Commun., 2015, 51, 16573 DOI: 10.1039/C5CC06069A

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