Issue 48, 2022
From the journal:

Chemical Communications

Anodic dearomatization of 2-alkynylanilines for the synthesis of multi-functionalized indoles†

Zhuowen Chen,a   Qiuqin He,b   Hao Guo ORCID logo *ab  and  Renhua Fan ORCID logo *b  

* Corresponding authors

a Academy for Engineering and Technology, Fudan University, 220 Handan Road, Shanghai 200433, China

b Department of Chemistry, Fudan University, 2005 Songhu Road, Shanghai 200438, China

Abstract

An anodic oxidative dearomatization reaction of 2-alkynylanilines was developed. The formed dearomatized compounds were used as versatile precursors in the synthesis of a variety of benzenoid ring multi-functionalized indoles through simple conversions.

Graphical abstract: Anodic dearomatization of 2-alkynylanilines for the synthesis of multi-functionalized indoles

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/D2CC01766K
Article type
Communication
Submitted
28 Mar 2022
Accepted
18 May 2022
First published
19 May 2022

Chem. Commun., 2022,58, 6797-6800

Permissions

Request permissions

Anodic dearomatization of 2-alkynylanilines for the synthesis of multi-functionalized indoles

Z. Chen, Q. He, H. Guo and R. Fan, Chem. Commun., 2022, 58, 6797 DOI: 10.1039/D2CC01766K

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