634-41-3Relevant articles and documents
Nickel-Catalyzed Amination of Aryl Nitriles for Accessing Diarylamines through C?CN Bond Activation
Wu, Ke,Rong, Qiang,Sun, Nan,Hu, Baoxiang,Shen, Zhenlu,Jin, Liqun,Hu, Xinquan
, p. 4708 - 4713 (2021/08/27)
A nickel-catalyzed amination to access diarylamines has been developed through C?CN bond activation of aryl nitriles with anilines. In this developed catalytic protocol, various aromatic and heteroaromatic nitriles could be utilized as the electrophiles to couple with substituted anilines. A diversity of diarylamines were obtained in 15–95% yields. (Figure presented.).
Organic electroluminescent material and synthesis and application thereof
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Paragraph 0068; 0071-0073; 0077; 0080-0082; 0086; 0089-0091, (2018/11/03)
The invention relates to the field of organic light-emitting diode (OLED) display, and particularly relates to an organic electroluminescent material and synthesis and application thereof. A general structure formula of the organic electroluminescent mate
Recyclable catalysts for palladium-catalyzed aminations of aryl halides
Dumrath, Andreas,Luebbe, Christa,Neumann, Helfried,Jackstell, Ralf,Beller, Matthias
experimental part, p. 9599 - 9604 (2011/10/04)
Aminated and recycled: Palladium/imidazolium phosphane catalysts enable efficient and general aminations of aryl halides, including direct amination with ammonia. Subsequent recycling is possible without any additional heterogenization (see scheme).