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Regiospecific epoxide opening: a facile approach for the synthesis of 3-hydroxy-3-aminomethylindolin-2-one derivatives
84
Citations
71
References
2011
Year
Reaction RateEngineeringGreen ChemistryFacile ApproachOrganic ChemistryChemistryEpoxide RingStereoselective SynthesisBiochemistryCatalysisRegiospecific Epoxide OpeningAsymmetric CatalysisNatural Product SynthesisEnantioselective SynthesisEco-friendly MethodBiomolecular EngineeringAlkene MetathesisNatural SciencesSynthetic Chemistry
A mild and eco-friendly method has been developed for aminolysis of 3-oxirane-indolin-2-ones with aliphatic and aromatic amines to afford 3-hydroxy-3-aminomethylindolin-2-ones. An enhancement in reaction rate was observed when water was used as the reaction medium. The reactions proceed regiospecifically to open the epoxide ring from the less-substituted end.
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