Issue 22, 2021

Nickel-catalyzed C3-alkylation of indoles with alcohols via a borrowing hydrogen strategy

Abstract

An efficient method for the Ni-catalyzed C3-alkylation of indoles using readily available alcohols as the alkylating reagents has been developed. The alkylation was addressed with an air and moisture-stable binuclear nickel complex ligated by tetrahydroquinolin-8-one as the effective pre-catalyst. The newly developed transformation could accommodate a broad substrate scope including primary/secondary benzylic and aliphatic alcohols and substituted indoles. Mechanistic studies suggested that the reaction proceeds through a borrowing hydrogen pathway.

Graphical abstract: Nickel-catalyzed C3-alkylation of indoles with alcohols via a borrowing hydrogen strategy

Supplementary files

Article information

Article type
Paper
Submitted
01 Apr 2021
Accepted
04 May 2021
First published
04 May 2021

New J. Chem., 2021,45, 10057-10062

Nickel-catalyzed C3-alkylation of indoles with alcohols via a borrowing hydrogen strategy

M. Hu, Y. Jiang, N. Sun, B. Hu, Z. Shen, X. Hu and L. Jin, New J. Chem., 2021, 45, 10057 DOI: 10.1039/D1NJ01581H

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