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Divergent Synthesis of Quinazolin-4(3<i>H</i>)-ones and Tryptanthrins Enabled by a <i>tert</i>-Butyl Hydroperoxide/K<sub>3</sub>PO<sub>4</sub>-Promoted Oxidative Cyclization of Isatins at Room Temperature
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Citations
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References
2016
Year
Tryptanthrin DerivativesDiversity Oriented SynthesisTryptanthrins EnabledBiochemistryOxidative CyclizationNatural SciencesMedicineAvailable IsatinsOrganic ChemistryDivergent SynthesisChemistrySynthetic UtilityHeterocycle ChemistryPharmacologySynthetic ChemistryBiomolecular EngineeringDrug Discovery
A synergetic tert-butyl hydroperoxide/K3PO4-promoted oxidative cyclization has been developed for the facile synthesis of various functionalized quinazolin-4(3H)-ones from commercially available isatins and amidine hydrochlorides at room temperature. The synthetic utility of this strategy was illustrated by the convenient synthesis of tryptanthrin derivatives via a self-dimerization of isatins under the same conditions.
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