Abstract
A one-pot, four-component reaction of 1-(phenylsulfinyl)- or 1-(4-chlorophenylsulfinyl)propan-2-one, aromatic aldehydes and ammonium acetate in a 1:2:1 molar ratio affords a series of new 2,6-diaryl-2,3-dihydro-1 H-pyridin-4-ones. This reaction proceeds presumably via a double Mannich reaction–elimination tandem sequence.
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