Acid chlorides and alkyl and aryl isocyanates and isothiocyanates were allowed to react with imines derived from cyclohexanone and isobutyraldehyde. A variety of N-(1-alkeny1) amides (2, 8), N-(1-alkeny1) ureas and thioureas (3, 5, 12), 2-enaminocarbamides (4, 6), and triazinones (11) were formed and isolated as reaction products, depending upon the nature of the imine, type of electrophile, and reaction conditions. The results are compared ...
