A novel one-pot three-step synthesis of 2-(1-benzofuran-2-yl)quinoline-3- carboxylic acid derivatives

18Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

Abstract

A facile and efficient one-pot three-step procedure for the preparation of 2-(1-benzofuran- 2-yl)quinoline-3-carboxylic acid derivatives is described, featuring three different synthetic transformations, namely Williamson ether synthesis, hydrolysis of an ester group at the quinoline ring C-3 position, and intramolecular electrophilic cyclization reaction between the aldehyde group of salicylaldehyde and the methylene at the quinoline ring C-2 position. © 2010 Sociedade Brasileira de Química.

Author supplied keywords

Cite

CITATION STYLE

APA

Gao, W., Zhang, C., & Li, Y. (2010). A novel one-pot three-step synthesis of 2-(1-benzofuran-2-yl)quinoline-3- carboxylic acid derivatives. Journal of the Brazilian Chemical Society, 21(5), 806–812. https://doi.org/10.1590/S0103-50532010000500007

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free