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A. Pastor, R. Alajarin, J. J. Vaquero, J. Alvarez-Builla, M. F. d. Casa-Juana, C. Sunkel, J. G. Priego, I. Fonseca and J. Sanz-Aparicio, “Synthesis and Structure of New Pyrido[2,3-d]pyrimidine Derivatives with Calcium Channel Antagonist Activity,” Tetrahedron, Vol. 50, No. 27, 1994, pp. 8085-8098. doi:10.1016/S0040-4020(01)85291-1

has been cited by the following article:

• TITLE: An Efficient Synthesis of Pyrido[2,3-d]pyrimidine Derivatives via One-Pot Three-Component Reaction in Aqueous Media

  AUTHORS: Shahrzad Abdolmohammadi, Saeed Balalaie

  KEYWORDS: Diammonium Hydrogen Phosphate (DAHP), Microwave Irradiation (MWI), Water in Organic Synthesis, Pyrido[2, 3-d]pyrimidine

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.2 No.1, March 15, 2012

  ABSTRACT: A series of pyrido[2,3-d]pyrimidines derivatives have been prepared by one-pot three-component reaction of 4(6)-aminouracil, malononitrile and aromatic aldehydes. This efficient synthesis was done under microwave irradiation conditions (method A) and also using catalytic amount of diammonium hydrogen phosphate [(NH4)2HPO4] (DAHP) in aqueous media (method B). This procedure has the advantages of good yields, easy work-up, and benign environmentally friendly character. Reaction could proceed via domino Knoevenagel-Michael-cyclization reactions.