Chemical Communications · 2013 · 45 citations · 41 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisAlkylation ProcessesAlkylation ReactionsEnantioselective CatalysisEnantioselective SynthesisLewis Acid CatalysisLewis AcidityPhase-transfer CatalysisSubstrate Scope
Highly enantioselective phase-transfer alkylation of 3-substituted-2-oxindoles with activated bromomethanes is disclosed with a broad substrate scope by using bicyclic guanidinium as a catalyst and a Lewis acid as the co-catalyst. The alkylation adducts are versatile intermediates to accomplish the syntheses of pyrroloindolines and furoindolines.
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Joel F. Austin, Sung-Gon Kim, Christopher J. Sinz et al. · Proceedings of the National Academy of Sciences · 2004 · 464 citations · Full text
Tommy Bui, Salahuddin Syed, Carlos F. Barbas · Journal of the American Chemical Society · 2009 · 348 citations