An efficient catalytic amination of aryl-substituted allylic alcohols has been developed. The complex [(eta(3)-allyl)PdCl](2) modified by a bis phosphine ligand, L, has been used as catalyst in the reaction that afforded a wide range of allyl amines in good to excellent yield under mild conditions.
An Unexpected Construction of 2-Arylquinolines from <i>N</i>
-Cinnamylanilines through <i>sp</i>
<sup>3</sup>
CH Aerobic Oxidation Induced by a Catalytic Radical Cation Salt
An unexpected reaction of cinnamylanilines was achieved through the radical cation salt‐induced aerobic oxidation of sp3 CH bonds, providing a series of 2‐arylquinolines. The mechanistic study shows that the cinnamylaniline was oxidized to an imine, which was attacked by the aniline generated through decomposition of the corresponding imine. After further intramolecular cyclization and aromatization
An efficient catalytic amination of aryl-substituted allylic alcohols has been developed. The complex [(eta(3)-allyl)PdCl](2) modified by a bis phosphine ligand, L, has been used as catalyst in the reaction that afforded a wide range of allyl amines in good to excellent yield under mild conditions.