An efficient chemoselective hydrogenation protocol for substituted cinnamic esters is developed for the synthesis in quantitative yield of corresponding bioactive dihydrocinnamic esters with solid-supported palladium chloride/ammonium formate (cat.) in HCOOH/H 2 O 1 : 2 as a hydrogenating agent under focused-microwave irradiation for 10 min.Introduction. -Environmental constrains [1] have led to the development of new chemical processes employing microwave, ultrasound, ionic liquids, recyclable catalysts and reagents, and biotransformations, etc. Catalysts and reagents on solid support under solventless (solvent-free) conditions is an especially important development of 'green' technologies which have made landmark contributions to preserve environment due to elimination of complicated workup procedures and reduction in waste effluent (more than 15 billion kg of solvent consumed worldwide annually!) [2]. Further, use of microwave irradiation on solid-supported reactions has enhanced the impact of the latter as the high heating efficiency of microwave results in remarkable rate enhancement, higher yields, greater selectivity, and ease of manipulation of such reactions [3]. In addition, the limitation of the microwave-assisted reactions in solvents enforcing development of high pressure and special sealed vessels are circumvented by this solid-support strategy [4], which enables organic reactions such as oxidation, hydrogenation, etc., to occur rapidly at atmospheric pressure and to upscale the reaction on a preparative scale.A lot of hydrogenation protocols are available for the selective hydrogenation of C=C bonds of unsaturated esters which either require a special apparatus and H 2 gas (potentially explosive) [5]