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Herein we report the WO
Dipic(H
O) promoted oxyamination of alkenes using sulfonamides as the quantitative source of
. The reaction works for activated and unactivated alkenes in high yields, diastereoselectivities, and stereospecificity. A catalytic cycle involving the formation of tungstenooxaziridine complex 1 as the active catalyst and hydrolysis of tungstenooxazolidine intermediate
as the rate-determining-step has been proposed. Initial kinetic and competition experiments provide evidence for the proposed mechanism.