Issue 19, 2021

Visible-light-driven photocyclization reaction: photocatalyst-free mediated intramolecular N–N coupling for the synthesis of 2H-indazole-3-carboxamides from aryl azides

Abstract

In this report, a visible-light-driven photocyclization reaction of aryl azides to access 2H-indazole-3-carboxamides in moderate to excellent yields has been realized efficiently under photocatalyst-free and external additive-free conditions. An N–N bond coupling was achieved for this N-atom incorporation transformation using an aryl azide as the N-atom source. The transformation of the aryl azide by photocyclization was also achieved under sunlight irradiation. Additionally, this protocol, as a green and sustainable process, possesses some advantages such as broad substrate scope, step- and atom-economy, environmental friendliness and mild reaction conditions.

Graphical abstract: Visible-light-driven photocyclization reaction: photocatalyst-free mediated intramolecular N–N coupling for the synthesis of 2H-indazole-3-carboxamides from aryl azides

Supplementary files

Article information

Article type
Research Article
Submitted
18 May 2021
Accepted
12 Jul 2021
First published
13 Jul 2021

Org. Chem. Front., 2021,8, 5296-5302

Visible-light-driven photocyclization reaction: photocatalyst-free mediated intramolecular N–N coupling for the synthesis of 2H-indazole-3-carboxamides from aryl azides

J. Liu, N. Liu, Q. Yang and L. Wang, Org. Chem. Front., 2021, 8, 5296 DOI: 10.1039/D1QO00777G

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