An efficient catalyst-free protocol for the synthesis of quinoxaline derivatives under ultrasound irradiation

67Citations
Citations of this article
29Readers
Mendeley users who have this article in their library.

Abstract

A highly efficient and facile method has been described for the synthesis of quinoxaline derivatives in good to excellent yields (80-99%) by condensation reaction of heterocyclic as well as aliphatic 1,2-diketones (R1COCOR1, R1 = Et, Ph, p-MeC6H5, p-MeOC6H5, Furyl) with 1,2-diamines (1,2-(NH2)2C6H3R2, R2 = H, Br, NO2, PhCO). A systematic study was carried out to examine the influence of reaction media and electronic factors of the substrates on the reaction results. © 2009 Sociedade Brasileira de Química.

Cite

CITATION STYLE

APA

Guo, W. X., Jin, H. L., Chen, J. X., Ding, F. C., & Wu, H. Y. (2009). An efficient catalyst-free protocol for the synthesis of quinoxaline derivatives under ultrasound irradiation. Journal of the Brazilian Chemical Society, 20(9), 1674–1679. https://doi.org/10.1590/S0103-50532009000900016

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