Bromide-catalyzed oxo-amination of alkenes towards the synthesis of α-amine ketones under photoelectrocatalysis conditions

Abstract

An efficient and novel bromide-catalyzed oxo-amination of aryl alkenes towards the synthesis of α-amine ketones using air as the oxygen source under photoelectrocatalysis conditions was developed. The reaction was characterized by simple operation, a broad substrate scope, high atom economy, and mild reaction conditions. The mechanistic results suggested that the generation of 2-bromo-1-phenylethanone via oxo-bromination of aryl alkenes was the key step in this transformation.

Graphical abstract: Bromide-catalyzed oxo-amination of alkenes towards the synthesis of α-amine ketones under photoelectrocatalysis conditions

Supplementary files

Article information

Article type
Research Article
Submitted
27 Feb 2024
Accepted
10 May 2024
First published
14 May 2024

Org. Chem. Front., 2024, Advance Article

Bromide-catalyzed oxo-amination of alkenes towards the synthesis of α-amine ketones under photoelectrocatalysis conditions

Z. Zong, M. Wang, X. Zhao and Y. He, Org. Chem. Front., 2024, Advance Article , DOI: 10.1039/D4QO00369A

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