Issue 49, 2019

N-Heterocyclic carbene copper catalyzed quinoline synthesis from 2-aminobenzyl alcohols and ketones using DMSO as an oxidant at room temperature

Abstract

A facile and practical process for the synthesis of quinolines through an N-heterocyclic carbene copper catalyzed indirect Friedländer reaction from 2-aminobenzyl alcohol and aryl ketones using DMSO as an oxidant at room temperature is reported. A series of quinolines were synthesized in acceptable yields.

Graphical abstract: N-Heterocyclic carbene copper catalyzed quinoline synthesis from 2-aminobenzyl alcohols and ketones using DMSO as an oxidant at room temperature

Supplementary files

Article information

Article type
Paper
Submitted
30 Jun 2019
Accepted
29 Aug 2019
First published
12 Sep 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 28764-28767

N-Heterocyclic carbene copper catalyzed quinoline synthesis from 2-aminobenzyl alcohols and ketones using DMSO as an oxidant at room temperature

J. Xu, Q. Chen, Z. Luo, X. Tang and J. Zhao, RSC Adv., 2019, 9, 28764 DOI: 10.1039/C9RA04926F

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