Palladium-catalyzed reductive coupling of phenols with anilines and amines: efficient conversion of phenolic lignin model monomers and analogues to cyclohexylamines
coupling reaction of nitroarenes with phenols has been developed. A series of N-cyclohexylaniline derivatives was easily and efficiently obtained in moderate to good yields via C–N bond formation by the simple use of safe and inexpensive sodiumformate as the hydrogen donor. A direct and efficient palladium-catalyzed reductive coupling reaction of nitroarenes with phenols has been developed. A series of
Palladium-catalyzed reductive coupling of phenols with anilines and amines: efficient conversion of phenolic lignin model monomers and analogues to cyclohexylamines
作者:Zhengwang Chen、Huiying Zeng、Hang Gong、Haining Wang、Chao-Jun Li
DOI:10.1039/c5sc00941c
日期:——
A highly efficient Pd-catalyzed direct coupling of phenolic lignin model monomers and analogues with anilines to give cyclohexylamines using sodium formate as hydrogen donor is described.