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Direct Access to Alkylideneoxindoles via Axially Enantioselective Knoevenagel Condensation
Simone Crotti1, Nicola Di Iorio1, Chiara Artusi1
1Department of Industrial Chemistry "Toso Montanari" University of Bologna , Viale del Risorgimento 4 , 40136 , Bologna , Italy.
Abstract:
The organocatalytic axially enantioselective Knoevenagel condensation between prochiral cyclohexanones and oxindoles is presented. The reaction, promoted by a primary amine, proceeded smoothly and furnished unprecedented examples of novel cyclohexylidene oxindoles displaying axial chirality.
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