Xu Qi, Zhang Huan, Ge Fang-Bei, Wang Xiao-Mei, Zhang Peng, Lu Chuan-Jun, Liu Ren-Rong
College of Chemistry and Chemical Engineering, Qingdao University, Qingdao 266071, P. R. China.
Org Lett. 2022 May 6;24(17):3138-3143. doi: 10.1021/acs.orglett.2c00812. Epub 2022 Apr 22.
We report herein that copper(I) catalysis using a bis(phosphine) dioxide ligand can catalyze the desymmetric C-H arylation of prochiral bipyrroles. More than 50 nitrogen-nitrogen atropisomers were achieved in good to excellent yields with excellent enantioselectivities (≤97% yield, ≤98% ee). The reaction proceeds under mild conditions with good functional group compatibility on arenes and diaryliodonium salts. Moreover, this principle enables iterative arylation of the bipyrroles to enantioselectively arylate different positions during the catalysis of copper.
我们在此报告,使用双(二氧化膦)配体的铜(I)催化能够催化前手性联吡咯的去对称C-H芳基化反应。以良好至优异的产率和出色的对映选择性(产率≤97%,对映体过量值≤98%)得到了50多种氮-氮阻转异构体。该反应在温和条件下进行,对芳烃和二芳基碘鎓盐具有良好的官能团兼容性。此外,这一原理能够对联吡咯进行迭代芳基化,从而在铜催化过程中对不同位置进行对映选择性芳基化。