Abstract

An efficient five-component condensation reaction of isatin, malononitrile, secondary amines, alcohols, and molecular oxygen was discovered. The reaction was performed in a one-pot fashion, and it does not require any metal catalyst. It gives straightforward access to structurally diverse 2-oxo-3-aminoindoline-3-carboxylates in moderate yields (70-88%). The scope of the reaction was successfully demonstrated by synthesizing a series of 3-functionalized 2-oxindoles by varying the isatin, amine, and alcohol components.

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