Issue 45, 2017, Issue in Progress

Copper-catalyzed N-alkylation of indoles by N-tosylhydrazones

Abstract

An efficient method for the direct N-alkylation of indoles via copper-catalyzed reductive cross coupling between N-tosylhydrazones and indole reagents has been developed. The reaction was performed in the presence of copper iodide and potassium hydroxide by utilization of tri(p-tolyl)phosphine as a ligand. A wide variety of N-alkylated indoles were obtained in moderate to good yields. The application of the current method to the synthesis of biologically active N-alkylated indole derivatives has also been demonstrated.

Graphical abstract: Copper-catalyzed N-alkylation of indoles by N-tosylhydrazones

Supplementary files

Article information

Article type
Paper
Submitted
01 Apr 2017
Accepted
17 May 2017
First published
26 May 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 27974-27980

Copper-catalyzed N-alkylation of indoles by N-tosylhydrazones

L. Ling, J. Cao, J. Hu and H. Zhang, RSC Adv., 2017, 7, 27974 DOI: 10.1039/C7RA03765A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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