Montmorillonite K10-Catalyzed Aza Diels-Alder Reaction of Danishefsky’s Diene with Aldimines, Generated in situ from Aliphatic Aldehydes and Amine, in Aqueous Media

Abstract
The montmorillonite K10-catalyzed aza Diels-Alder reaction of Danishefsky’s diene with aldimines, generated in situ from aliphatic aldehydes and p-anisidine, proceeded smoothly in H2O or in aqueous CH3CN to afford 2-substituted 2,3-dihydro-4-pyridones in excellent yields.

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