Issue 63, 2019

A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin

Abstract

A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters has been developed through an AlCl3-catalyzed reaction of easily available Baylis–Hillman adducts from chromones and isatin-derivatives. This reaction involves esterification, cyclization and ring opening in a one-step process, and provides an efficient approach for easy access to a series of valuable salicyloylquinoline derivatives with high yields. Moreover, this protocol offers several advantages, such as availability of starting materials, economic availability, operational simplicity and mild reaction conditions.

Graphical abstract: A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin

Supplementary files

Article information

Article type
Paper
Submitted
07 Oct 2019
Accepted
28 Oct 2019
First published
12 Nov 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 37057-37060

A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin

X. Wang, Z. Yang, W. Miu, P. Ye, M. Bai, S. Duan and X. Shen, RSC Adv., 2019, 9, 37057 DOI: 10.1039/C9RA08124K

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements