| Literature DB >> 26531683 |
Zhengwang Chen1,2, Huiying Zeng1, Simon A Girard1, Feng Wang1, Ning Chen1, Chao-Jun Li3.
Abstract
The transition-metal-catalyzed amination of aryl halides has been the most powerful method for the formation of aryl amines over the past decades. Phenols are regarded as ideal alternatives to aryl halides as coupling partners in cross-couplings. An efficient palladium-catalyzed formal cross-coupling of phenols with various amines and anilines has now been developed. A variety of substituted phenols were compatible with the standard reaction conditions. Secondary and tertiary aryl amines could thus be synthesized in moderate to excellent yields.Entities:
Keywords: aryl amines; dehydrogenation; hydrogen borrowing; palladium; phenols
Year: 2015 PMID: 26531683 DOI: 10.1002/anie.201506751
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336