Fast and convenient synthesis of new symmetric pyrano[2,3-d:6,5-d']dipyrimidinones by an organocatalyzed annulation reaction

26Citations
Citations of this article
2Readers
Mendeley users who have this article in their library.

Abstract

A fast and facile one-pot procedure for the preparation of symmetric 5-Aryloyl-1,9-dimethyl- 5,9-dihydro-2H-pyrano[2,3-d:6,5-d']dipyrimidine-2,4,6,8(1H,3H,7H)-tetraone derivatives by two-component reaction of N-methylbarbituric acid and arylglyoxalmonohydrates catalyzed by DABCO in ethanol at 50 ºC is described. This protocol has the advantages of environmental friendless, very simple operation, high regio- and chemoselectivity and moderate to excellent yields.

Cite

CITATION STYLE

APA

Rimaz, M., Mousavi, H., Behnam, M., Sarvari, L., & Khalili, B. (2017). Fast and convenient synthesis of new symmetric pyrano[2,3-d:6,5-d’]dipyrimidinones by an organocatalyzed annulation reaction. Current Chemistry Letters, 6(2), 55–68. https://doi.org/10.5267/j.ccl.2016.12.001

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