Issue 59, 2018, Issue in Progress

Transition metal/Brønsted acid cooperative catalysis enabled facile synthesis of 8-hydroxyquinolines through one-pot reactions of ortho-aminophenol, aldehydes and alkynes

Abstract

A convenient and straightforward three-component one-pot strategy has been developed for the synthesis of 8-hydroxyquinoline derivatives. Under the cooperative catalysis of silver(I) triflate and trifluoroacetic acid, ortho-aminophenol reacted with a range of aldehydes and alkynes under mild reactions, affording the corresponding 8-hydroxyquinoline derivatives with good to excellent yields. These transformations exhibited exceptional substrate generality and functional group compatibility.

Graphical abstract: Transition metal/Brønsted acid cooperative catalysis enabled facile synthesis of 8-hydroxyquinolines through one-pot reactions of ortho-aminophenol, aldehydes and alkynes

Supplementary files

Article information

Article type
Paper
Submitted
29 Aug 2018
Accepted
24 Sep 2018
First published
03 Oct 2018
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2018,8, 33968-33971

Transition metal/Brønsted acid cooperative catalysis enabled facile synthesis of 8-hydroxyquinolines through one-pot reactions of ortho-aminophenol, aldehydes and alkynes

S. Yu, J. Wu, H. Lan, H. Xu, X. Shi, X. Zhu and Z. Yin, RSC Adv., 2018, 8, 33968 DOI: 10.1039/C8RA07212D

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