Issue 18, 2019, Issue in Progress

An efficient 3-acylquinoline synthesis from acetophenones and anthranil via C(sp3)–H bond activation mediated by Selectfluor

Abstract

An efficient method for the synthesis of 3-functionalized quinolines from commercially available acetophenones and anthranil has been described. Selectfluor propels the C(sp3)–H bond activation of the acetophenones and aza-Michael addition of anthranil resulting in annulated 3-acylquinolines in moderate to high yields. DMSO acts not only as a solvent but also as a one carbon donor in the reaction.

Graphical abstract: An efficient 3-acylquinoline synthesis from acetophenones and anthranil via C(sp3)–H bond activation mediated by Selectfluor

Supplementary files

Article information

Article type
Paper
Submitted
27 Feb 2019
Accepted
27 Mar 2019
First published
02 Apr 2019
This article is Open Access
Creative Commons BY license

RSC Adv., 2019,9, 10340-10344

An efficient 3-acylquinoline synthesis from acetophenones and anthranil via C(sp3)–H bond activation mediated by Selectfluor

Y. Gao, R. C. Hider and Y. Ma, RSC Adv., 2019, 9, 10340 DOI: 10.1039/C9RA01481K

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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