Herein, we describe an efficient, rapid and benign protocol for the direct C(sp 2 )–H bond halogenation (Cl, Br, I) of 2-arylimidazo[1,2- a ]pyridines using trihaloisocyanuric acids in ethanol.
Herein, we report an efficient, quick and eco-friendly new method for the synthesis of a variety of selenol esters. This novel solvent-free methodology gave good to excellent isolated yields of desired products after just 2 min under microwave irradiation. Furthermore, by using the same green approach, we were also able to synthesize selenocarbonates bearing interesting functionalities.
The efficient and mild copper-catalyzed synthesis of unsymmetrical diorganyl chalcogenides under ligand- and solvent-free conditions is described. The cross-coupling reaction was performed using aryl boric acids and 0.5 equiv. of diorganyl dichalcogenides (Te/Se/S) in the presence of 3 mol % of CuI and 3 equiv. of DMSO, under microwave irradiation. This new protocol allowed the preparation of several unsymmetrical diorganyl chalcogenides in good to excellent yields.
27 April 2010 in European Journal of Organic Chemistry