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.
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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
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