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Solvent‐Free Synthesis of 4<i>H</i>‐Pyrido[1,2‐<i>a</i>]pyrimidin‐4‐ones Catalyzed by BiCl<sub>3</sub>: A Green Route to a Privileged Backbone
22
Citations
38
References
2015
Year
Diversity Oriented SynthesisEngineeringAvailable 2‐AminopyridinesNatural SciencesPrivileged BackboneDiversity-oriented SynthesisExtensive ArrayOrganic ChemistryCatalysisChemistrySolvent‐free SynthesisGreen ReactionHeterocycle ChemistrySynthetic ChemistryBiomolecular EngineeringGreen Route
Abstract An extensive array of 4 H ‐pyrido[1,2‐ a ]pyrimidin‐4‐ones have been synthesized from commercially available 2‐aminopyridines and β‐oxo esters with excellent yields under solvent‐free conditions. The reaction, catalyzed by cheap and nontoxic BiCl 3 , proceeds with short reaction times under mild conditions and normal atmosphere. Only water and alcohol are formed as co‐products in this green reaction.
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