Issue 23, 2017

Electrocatalytic intramolecular oxidative annulation of N-aryl enamines into substituted indoles mediated by iodides

Abstract

An electrocatalytic reaction protocol is developed for achieving intramolecular dehydrogenative annulation of N-aryl enamines. It offers a simple and efficient way for the synthesis of indoles in an undivided cell. Good to excellent yields are obtained under oxidant-free and transition-metal-free conditions. Moreover, imidazo[1,2-a]pyridines could also be produced when N-pyridyl enamines were used as the substrates.

Graphical abstract: Electrocatalytic intramolecular oxidative annulation of N-aryl enamines into substituted indoles mediated by iodides

Supplementary files

Article information

Article type
Communication
Submitted
17 Jan 2017
Accepted
24 Feb 2017
First published
24 Feb 2017

Chem. Commun., 2017,53, 3354-3356

Electrocatalytic intramolecular oxidative annulation of N-aryl enamines into substituted indoles mediated by iodides

S. Tang, X. Gao and A. Lei, Chem. Commun., 2017, 53, 3354 DOI: 10.1039/C7CC00410A

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