“…In addition several synthetic tetrahydropyridines have been shown to display important biological activities. On the other hand, 2,3,5-trisubstituted pyrroles have also been studied to exhibit significant biological activities. , The tetrahydropyridines and pyrroles may be synthesized via a number of classical methods that also include the treatment of allylic alcohols with potassium bis(trimethylsilyl)amide, − intermolecular amido carbonylation of carbomates, and intramolecular condensations of aldehydes with enamides. Several methods, such as transition metal-catalyzed cycloadditions, coupling of enamides with alkynes, and oxidative cyclization of N -allyamines are available for the syntheses of polysubstituted pyrroles. − However, most of these methods have drawbacks, such as the use of expensive reagents or catalysts, lower yields, and poor selectivity.…”