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2000
Volume 11, Issue 6
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A solvent-free approach for the synthesis of a series of pyrimido[5',4':5,6]pyrido[2,3-d]pyrimidinetetraone and 4-arylacridinedione derivatives is described herein. These compounds having biological importance were prepared via a condensation reaction of aryl aldehydes, ammonium acetate and active methylene compounds including 1,3- dimethylbarbituric acid or dimedone under solvent-free conditions, using Zr(HPO4)2.H2O (α-ZrP) as an efficient catalyst. The reusability of catalyst and easier isolation of the products along with high yields of products are the advantages of this eco-friendly and versatile protocol.

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/content/journals/loc/10.2174/1570178611666140124002242
2014-07-01
2025-10-07
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/content/journals/loc/10.2174/1570178611666140124002242
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