Journal of Saudi Chemical Society · 2021 · 11 citations · 32 references
Natural SciencesChemistryMedicinal ChemistryCatalysisGreen ChemistrySynthetic Medicinal ChemistryDiversity-oriented SynthesisOrganic SynthesisChemical SubstituentsOne-pot Library SynthesisPurine ChemistryPyrimidine AnalogsPyrimidine AnaloguesPyrimidine Chemistry
A straightforward, cost effective and eco-friendly protocol for the Biginelli reaction relying on the use of readily available hypophosphorous acid is presented. The methodology developed displays improvements compared to existing methods, is high-yielding, robust and was applied to a panel of dihydropyrimidines and thio-derivatives with various substituents. Related urea derivatives such as guanidines, benzimidazoles and benzothiazoles also reacted efficiently to afford more complex scaffolds. Thus, this rapid and convenient catalysis allows access to a wide diversity of structures including original biologically relevant heterocycles.
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100 years of the biginelli dihydropyrimidine synthesis
C. Oliver Kappe · Tetrahedron · 1993 · 1.2K citations
George C. Rovnyak, Karnail S. Atwal, Anders Hedberg et al. · Journal of Medicinal Chemistry · 1992 · 451 citations
Karnail S. Atwal, George C. Rovnyak, S. David Kimball et al. · Journal of Medicinal Chemistry · 1990 · 378 citations