“…The success of these calcium antagonists has led to the development of several novel synthetic strategies along with improved classical methods of preparation, which include the use of microwaves, [12,13] ionic liquids, [14] metal triflates, [15] solvent reflux at high temperature, [16] TMSCl-NaI, [17] InCl 3 , [18] I 2 , [19] SiO 2 =HClO 4 , [20] SiO 2 = NaHSO 4 , [21] ceric ammounium nitrate (CAN), [22] Na-and Cs-norit carbons, [23] tetrabutylammonium hydrogen sulfate, [24] fermenting Baker's yeast, [25] and application of organocatalysts, [26] solar thermochemical method, [27] potassium dodecatungstocobaltate trihydrate, [28] thiamine hydrochloride, [29] and triphenylphosphine. [30] However, conditions such as the use of high temperature, expensive metal precursors, and longer reaction time limit these methods to great extent.…”