Abstract
A variety of thiols were oxidised efficiently by a catalytic amount of Mn(III)-salophen 1 in the presence of urea hydrogen peroxide adduct 2 as a convenient and mild oxidant to afford the corresponding disulfides in high yields in quite short reaction times.
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Karami, B., Montazerozohori, M., & Habibi, M. H. (2006). Bis (salicylaldehyde-1,2-phenylene diimine)Mn(III) chloride (Mn(III)-salophen) catalysed oxidation of thiols to symmetrical disulfides using urea hydrogen peroxide (UHP) as mild and efficient oxidant. Journal of Chemical Research, (8), 490–492. https://doi.org/10.3184/030823406778256441
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