Issue 23, 2018

Copper-catalyzed oxidative coupling of quinoxalin-2(1H)-ones with alcohols: access to hydroxyalkylation of quinoxalin-2(1H)-ones

Abstract

An efficient copper-catalyzed protocol for the synthesis of hydroxyl-containing quinoxalin-2(1H)-ones from the radical reaction of quinoxalin-2(1H)-ones with alcohols was developed with moderate to good yields. Quinoxalin-2(1H)-ones were coupled with alkyl radicals through direct catalytic functionalization of the α sp3 C–H bond of alcohols. The methodology demonstrates a broad substrate scope, excellent functional group tolerance, high atom economy and high efficiency, thus enabling the preparation of diverse potentially valuable hydroxyl-containing quinoxalin-2(1H)-ones.

Graphical abstract: Copper-catalyzed oxidative coupling of quinoxalin-2(1H)-ones with alcohols: access to hydroxyalkylation of quinoxalin-2(1H)-ones

Supplementary files

Article information

Article type
Research Article
Submitted
08 Sep 2018
Accepted
11 Oct 2018
First published
12 Oct 2018

Org. Chem. Front., 2018,5, 3382-3390

Copper-catalyzed oxidative coupling of quinoxalin-2(1H)-ones with alcohols: access to hydroxyalkylation of quinoxalin-2(1H)-ones

J. Fu, J. Yuan, Y. Zhang, Y. Xiao, P. Mao, X. Diao and L. Qu, Org. Chem. Front., 2018, 5, 3382 DOI: 10.1039/C8QO00979A

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