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A. Kutyrev and T. Kappe, “Methanetricarboxylates as Key Reagents for the Simple Preparation of Heteroary- lcarboxamides with Potential Biological Activity. Part 2[1]. Reaction of Methanetricarbox-ylates with 2-Amino- pyridine, 2-Aminopyrimidine, 2-Aminothiazole and 2- Aminobenzothiazole,” Journal of Hete-rocyclic Chemistry, Vol. 36, No. 1, 1999, pp. 237-240. doi:10.1002/jhet.5570360136

has been cited by the following article:

• TITLE: A New and Efficient Method for the Synthesis of Pyrimido[2,1-b]Benzothiazole Derivatives

  AUTHORS: Fatemeh Chadegani, Fatemeh Darviche, Saeed Balalaie

  KEYWORDS: 4H-Pyrimido [2, 1-b] Benzothiazole; Tandem Knoevenagel-Michael Reaction; One-Pot Reaction; Green Chemistry

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

  ABSTRACT: The one-pot three-component reaction of 2-aminobenzothiazole, benzaldehyde derivatives and β-ketoester, β-diketone or malonate derivatives in solvent-free conditions provides the corresponding pyrimido [2,1-b] benzothiazole derivatives at 60?C in 60% - 72% yields without using any catalyst in an optimistic time.