78888-05-8Relevant 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.).
Method of adopting C-N coupling reaction to prepare dialkyl diphenylamine
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Paragraph 0014, (2018/12/03)
The invention discloses a method of adopting C-N coupling reaction to prepare dialkyl diphenylamine antioxidation additive and belongs to the field of lubricating oil. The method includes: mainly taking bromoalkylbenzene and alkylaniline as raw materials
Threefold cross-linked polystyrene-triphenylphosphane hybrids: Mono-P-ligating behavior and catalytic applications for aryl chloride cross-coupling and C(sp3)-H borylation
Iwai, Tomohiro,Harada, Tomoya,Hara, Kenji,Sawamura, Masaya
supporting information, p. 12322 - 12326 (2013/12/04)
Covalently bound polystyrene-phosphane hybrids were prepared by a method based on radical emulsion polymerization of styrenes in the presence of a tris(p-vinylphenyl)phosphane cross-linker. These hybrids favor mono-P-ligation to transition-metal complexes and are useful for challenging catalysis, such as Pd-catalyzed C-C/C-N couplings with unactivated chloroarenes and Ir- or Rh-catalyzed C(sp3)-H borylations. Copyright