Abstract:
A convenient synthesis of 1,2-dihydropyridine (1,2-DHP) has been developed from dienaminodioate and
an imine mediated by trifluoroacetic acid in a one-pot cascade synthesis. The advantages associated with
this transformation include conditions that are metal-free, room temperature, undistilled solvent, and
expeditious in excellent yields. The substrate scope has been demonstrated with various aromatic,
heteroaromatic, unsaturated aldehydes, and anilines, benzylic amines in impressive yields.