Abstract
AbstractA direct, one‐pot and regioselective access to N‐alkyl‐ and N‐aryl‐substituted 2‐pyridones is described from readily available β‐keto amides and either primary or secondary propargylic alcohols. This approach involves the combination of two different cooperative homogeneous and heterogeneous catalytic systems based on a transition metal oxide and a supported organocatalyst, respectively.
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