Publication | Closed Access
Catalyst- and solvent-free, pot, atom and step economic synthesis of tetrahydroquinazolines by an aza-Diels–Alder reaction strategy
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References
2014
Year
Microwave ReactorChemical EngineeringDerivative (Chemistry)DerivativesEngineeringAza-diels–alder Reaction StrategyOrganic Chemistry2,4-Disubstituted TetrahydroquinazolinesCatalysisSynthetic ChemistryChemistryFour-component Aza-diels–alder ReactionHeterocycle ChemistrySynthesis MethodMicrowave SynthesisEconomic Synthesis
2,4-Disubstituted tetrahydroquinazolines can be readily obtained <italic>via</italic> a four-component aza-Diels–Alder reaction inside a microwave reactor. The methodology developed is simple, catalyst- and solvent-free and can be tuned to get dihydroquinazoline derivatives.
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