Herein, we describe an interesting palladium-catalyzed protocol for the carbonylative synthesis of 3-substituted maleimides. By annulation of simple anilines with terminal alkynes under carbon monoxide pressure, the desired 3-substituted maleimides can be obtained in 50-85% yields. Additionally, with the addition of phosphine ligand, maleic acid isoimide can be obtained from the same substrates as well. With the presence of K 2 S 2 O 8 , the obtained maleic acid isoimide can be completely transformed to the corresponding maleimide.