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

A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters has been developed through an AlCl(3)-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...

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Autores principales: Wang, Xuequan, Yang, Zhixin, Miu, Weihang, Ye, Pingting, Bai, Mengjiao, Duan, Suyue, Shen, Xianfu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075531/
https://www.ncbi.nlm.nih.gov/pubmed/35539051
http://dx.doi.org/10.1039/c9ra08124k
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author Wang, Xuequan
Yang, Zhixin
Miu, Weihang
Ye, Pingting
Bai, Mengjiao
Duan, Suyue
Shen, Xianfu
author_facet Wang, Xuequan
Yang, Zhixin
Miu, Weihang
Ye, Pingting
Bai, Mengjiao
Duan, Suyue
Shen, Xianfu
author_sort Wang, Xuequan
collection PubMed
description A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters has been developed through an AlCl(3)-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.
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spelling pubmed-90755312022-05-09 A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin Wang, Xuequan Yang, Zhixin Miu, Weihang Ye, Pingting Bai, Mengjiao Duan, Suyue Shen, Xianfu RSC Adv Chemistry A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters has been developed through an AlCl(3)-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. The Royal Society of Chemistry 2019-11-12 /pmc/articles/PMC9075531/ /pubmed/35539051 http://dx.doi.org/10.1039/c9ra08124k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wang, Xuequan
Yang, Zhixin
Miu, Weihang
Ye, Pingting
Bai, Mengjiao
Duan, Suyue
Shen, Xianfu
A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin
title A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin
title_full A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin
title_fullStr A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin
title_full_unstemmed A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin
title_short A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin
title_sort simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075531/
https://www.ncbi.nlm.nih.gov/pubmed/35539051
http://dx.doi.org/10.1039/c9ra08124k
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