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An efficient palladium-catalyzed two-step protocol for the synthesis of Baylis–Hillman adducts of acrylamide was developed. The method involved the preparation of Baylis–Hillman adducts of acrylonitrile and a Pd-catalyzed hydration of nitrile with acetaldoxime.
An efficient palladium-catalyzed protocol for the hydration of nitrile to amide with acetaldoxime has been developed. A plausible mechanism was suggested involving the first Pd(II)-catalyzed nitrile–oxime coupling and the following disruption of the intermediate into amide and acetonitrile in a concerted manner.
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