State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , 345 Lingling Lu, Shanghai 200032, China.
J Am Chem Soc. 2016 Mar 2;138(8):2544-7. doi: 10.1021/jacs.6b00127. Epub 2016 Feb 22.
A Pd-catalyzed, asymmetric oxidative cross-coupling reaction between ferrocenes and heteroarenes is described. The process, which takes place via a twofold C-H bond activation pathway, proceeds with modest to high efficiencies (36-86%) and high levels of regio- and enantioselectivity (95-99% ee). In the reaction, air oxygen serves as a green oxidant and excess amounts of the coupling partners are not required. The process is the first example of a catalytic asymmetric biaryl coupling reaction that occurs via double C-H bond activation. Finally, the generated coupling products can be readily transformed into chiral ligands and catalysts.
描述了一种 Pd 催化的、不对称的氧化交叉偶联反应,该反应发生在双重 C-H 键活化途径中,具有中等至较高的效率(36-86%)和高水平的区域和对映选择性(95-99%ee)。在反应中,空气氧气作为一种绿色氧化剂,不需要过量的偶联试剂。该过程是首例通过双重 C-H 键活化发生的催化不对称联芳基偶联反应。最后,生成的偶联产物可以很容易地转化为手性配体和催化剂。