Publication | Closed Access
1-Hydroxybenzotriazole-Assisted, N-Heterocyclic Carbene Catalyzed β-Functionalization of Saturated Carboxylic Esters: Access to Spirooxindole Lactones
60
Citations
46
References
2016
Year
EngineeringOrganic ChemistryGram ScaleChemistryHeterocycle ChemistrySaturated Carboxylic EstersDirect β-FunctionalizationStereoselective SynthesisSpirooxindole LactonesDual RoleDiversity-oriented SynthesisCatalysisPharmacologyAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringHeterocyclicAlkene MetathesisNatural SciencesSynthetic Chemistry
A 1-hydroxybenzotriazole-assisted, N-heterocyclic carbene catalyzed direct β-functionalization of saturated carboxylic esters is disclosed. This formal [3 + 2] annulation reaction of carboxylic esters with isatins affords optically pure spirooxindole lactones (on gram scale) bearing two vicinal stereogenic centers. A dual role of HOBt is proposed based on controlled experiments to rationalize the enhancement of diastereoselectivity and enantioselectivity.
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