1374838-99-9Relevant academic research and scientific papers
Construction of the flavones and aurones through regioselective carbonylative annulation of 2-bromophenols and terminal alkynes
Liu, Jianming,Liu, Muwen,Yue, Yuanyuan,Zhang, Ningfei,Zhang, Yuanli,Zhuo, Kelei
supporting information, p. 1802 - 1807 (2013/04/24)
The easily available and efficient catalyst containing a benzimidazolium ligand and PdCl2(PPh3)2 demonstrated excellent catalytic activity to construct the flavones and aurones, respectively. This reaction can be operated under mild conditions, affording the desired products in moderate to good yields. This protocol was used to prepare the flavones and aurones by a slight modification of amines.
Environmental friendly azide-alkyne cycloaddition reaction of azides, alkynes, and organic halides or epoxides in water: Efficient "click" synthesis of 1,2,3-triazole derivatives by Cu catalyst
Liu, Jianming,Liu, Muwen,Yue, Yuanyuan,Yao, Meihuan,Zhuo, Kelei
experimental part, p. 644 - 650 (2012/05/20)
An efficient click synthesis of 1,2,3-triazole derivatives from benzyl halides or alkyl halides, epoxides, terminal alkynes, and sodium azides in the presence of copper salts and relative benzimidazole salts have been developed. This procedure eliminates the need to handle potentially organic azides, which are generated in situ. A broad spectrum of substrates can participate in the process effectively to produce the desired products in good yields.
