Department of Material Chemistry, Graduate School of Engineering, Kyoto University , Kyoto 615-8510, Japan.
Fukui Institute for Fundamental Chemistry, Kyoto University , Sakyo-ku, Kyoto 606-8103, Japan.
J Am Chem Soc. 2016 Nov 9;138(44):14699-14704. doi: 10.1021/jacs.6b08767. Epub 2016 Nov 1.
We report a method that ensures the selective alkylation of benzamides and aromatic ketones at the para-position via cooperative nickel/aluminum catalysis. Using a bulky catalyst/cocatalyst system allows reactions between benzamides and alkenes to afford the corresponding para-alkylated products. The origin of the high para-selectivity has also been investigated by density functional theory calculations.
我们报告了一种通过协同镍/铝催化选择性地在对位进行苯甲酰胺和芳香酮烷基化的方法。使用大位阻的催化剂/共催化剂体系,可以使苯甲酰胺与烯烃发生反应,得到相应的对位烷基化产物。通过密度泛函理论计算也研究了高对位选择性的起源。