Abstract
Synergistic organoboron/palladium cocatalysis enables dehydrative couplings of NH-sulfoximines with allylic alcohols, furnishing the corresponding N-allylated products. The reactions proceed in the absence of a Brønsted base and are tolerant of diverse sulfoximine partners, including functionalized variants. Experimental and computational studies suggest that the sulfoximine reagent is activated by complexation to the boronic acid cocatalyst.
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