A series of arylboronates has been synthesized from the reaction of 2-(2-,(3-, or (4- (bromomethyl) phenyl)-4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolane 1 {1− 3} respectively with a range of N-, S-, and O-nucleophiles, using microwave-mediated chemistry. For the synthesis of N-and S-substituted boronates, a supported base, PS-NMM, was employed, and many reactions were complete within 15 min. With O-nucleophiles, a mixture of ...