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Palladium-Catalyzed Direct Amination of Allylic Alcohols in Aqueous Media
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文摘
Palladium chloride-catalyzed amination of allylic alcohols with aromatic amines in the presence of triphenylphosphine and trifluoroacetic acid in the aqueous phase gave a wide range of allylamines in good to excellent yields under mild conditions. This protocol has a wide substrate scope and broad functional group tolerance. It is an environmentally friendly and highly atom-economical method for N-allylamine synthesis. A plausible mechanism involving a (π-allyl)palladium complex intermediate is proposed.

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