Dearomatizative Aminoetherification and Diamination of Indoles Enabled by Photochemical Nitrene Transfer Reactions

Abstract

In this study, we report a catalyst free, dearomatizative aminoetherification and diamination of indoles by using photo-promoted nitrene transfer reaction as the key step. A wide range of indoline scaffolds can be obtained in moderate to good yields. The approach can be further applied to the synthesis of three kinds of bioactive polycyclic ring structures. A series of mechanistic experiments well supports the proposed nitrene transfer process.

Supplementary files

Article information

Article type
Communication
Accepted
07 May 2025
First published
08 May 2025

Chem. Commun., 2025, Accepted Manuscript

Dearomatizative Aminoetherification and Diamination of Indoles Enabled by Photochemical Nitrene Transfer Reactions

L. Zhang, Y. Xie and J. Xuan, Chem. Commun., 2025, Accepted Manuscript , DOI: 10.1039/D5CC02416A

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