Abstract:The oxidation of dithioacetals with 16 eq of 30% hydrogen peroxide in the presence of 10 mol% niobium(V) chloride at room temperature provides bissulfonylmethylenes in high yields.
“…There is precedence for the application of niobium catalysts in oxidative processes that employ hydrogen peroxide as oxidant. Most examples involve the epoxidation of alkenes [17], but oxidation of dithioacetals, benzylalcohols, naphthols and sulfides [17][18][19][20][21] have also been reported. Reddy and Sayari demonstrated that vanadium was capable of catalyzing the oxidation of amines in the presence of hydrogen peroxide to afford the corresponding imines and oximes under mild conditions [22].…”
“…There is precedence for the application of niobium catalysts in oxidative processes that employ hydrogen peroxide as oxidant. Most examples involve the epoxidation of alkenes [17], but oxidation of dithioacetals, benzylalcohols, naphthols and sulfides [17][18][19][20][21] have also been reported. Reddy and Sayari demonstrated that vanadium was capable of catalyzing the oxidation of amines in the presence of hydrogen peroxide to afford the corresponding imines and oximes under mild conditions [22].…”
“…The previous treatment with hydrogen peroxide should generate peroxo groups on the catalyst surface, which makes the catalyst more active. [18][19][20][21] It is interesting to observe that the catalyst without previous treatment with hydrogen peroxide (Nb-MCM) showed an increase in the removal of rhodamine B after 30 min, indicating that after that time the H 2 O 2 added to the reaction system reacted with the surface Nb forming the peroxo group in situ. This result shows clearly that the previous treatment of the catalyst with H 2 O 2 increases the catalytic activity of the silica modified with niobium for oxidation of the organic compound.…”
Active catalysts for oxidation of non-selective organic compounds were produced by doping silica with niobium followed by treatment with hydrogen peroxide.
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