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 H 2 O or in aqueous CH 3 CN to afford 2-substituted 2,3-dihydro-4-pyridones in excellent yields.
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