Nickel??Catalyzed Electrochemical Arylation of Activated Olefins
…, D Dupré, G Falgayrac, JY Nédélec
Index: Condon, Sylvie; Dupre, Daniel; Falgayrac, Gilles; Nedelec, Jean-Yves European Journal of Organic Chemistry, 2002 , # 1 p. 105 - 111
Full Text: HTML
Citation Number: 17
Abstract
Abstract Nickel-catalyzed electrochemical conjugate additions of substituted aryl bromides to activated olefins under recently optimized reaction conditions are reported. Good to high yields were obtained, whatever the nature of substituents in the meta-and para-positions of the benzene ring. In the ortho-substituted series, yields were good with electron-donating substituents, but low with electron-withdrawing groups. The activation of aryl chlorides and ...
Related Articles:
α??Alkylation of Carbonyl Compounds by Direct Addition of Alcohols to Enol Acetates
[Nishimoto, Yoshihiro; Onishi, Yoshiharu; Yasuda, Makoto; Baba, Akio Angewandte Chemie - International Edition, 2009 , vol. 48, # 48 p. 9131 - 9134]
[Huang, Liangbin; Qi, Ji; Wu, Xia; Wu, Wanqing; Jiang, Huanfeng Chemistry - A European Journal, 2013 , vol. 19, # 46 p. 15462 - 15466]
[Zou, Gang; Guo, Jianping; Wang, Zhiyong; Huang, Wen; Tang, Jie Dalton Transactions, 2007 , # 28 p. 3055 - 3064]
[Synthesis, , # 15 p. 2415 - 2426]
InCl3/Me3SiBr-Catalyzed Direct Coupling between Silyl Ethers and Enol Acetates
[Organic Letters, , vol. 13, # 10 p. 2762 - 2765]