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Gao, X., Cen, L., Li, F., Wen, R., Yan, H., Yao, H. and Zhu, S. (2018) Oral Administration of Indole Substituted Dipyrido[2,3-d]pyrimidine Derivative Exhibits Anti-Tumor Activity via Inhibiting AKT and ERK1/2 on Hepatocellular Carcinoma. Biochemical and Biophysical Research Communications, 505, 761-767.
https://doi.org/10.1016/j.bbrc.2018.09.120

has been cited by the following article:

• TITLE: One-Pot Synthesis of Pyrido[2,3-d]pyrimidines Catalyzed by Bismuth(III)Triflate

  AUTHORS: Deniz Saglam, Zuhal Turgut

  KEYWORDS: Bismuth Triflate, Pyrido[2, 3-d]pyrimidine, One-Pot, Biological Activity

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.12 No.1, March 29, 2022

  ABSTRACT: Synthesis of uracil derivatives, such as pyrido[2,3-d]pyrimidine, is very important for the pharmaceutical industry due to their many biological activities. In our continuing efforts into the development of new synthetic strategies for the preparation of heterocyclic compounds in this study, we performed reflux reactions with the catalyst Bi(OTf)3 by using a one-pot, threecomponent method. The one-pot, three-component condensation of 6-amino-1,3-dimethyluracil, with arylaldehydes and malononitrile to generate a series of 7-aminopyrido[2,3-d]pyrimidine-6-carbonitrile derivatives has been carried out in the presence of bismuth triflate as a green and reusable catalyst.