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An intermolecular hydroamination of allenamides with arylamines catalyzed by cationic Au(I) salts
(Figure presented) An intermolecular hydroamination of allenamides with arylamines has been achieved under mild Au(I) catalysis conditions delivering allylamino E-enamides stereoselectively and in high yield. The reaction is made possible via a convenient method for conjugated N-acyliminium formation.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Recommanded Product: Oxazolidin-2-one, you can also check out more blogs about497-25-6
Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H609NO – PubChem