Yu Jianfei, Duan Meng, Wu Weilong, Qi Xiaotian, Xue Peng, Lan Yu, Dong Xiu-Qin, Zhang Xumu
College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei, 430072, P.R. China.
School of Chemistry and Chemical Engineering, Chongqing University, Chongqing, 400030, P.R. China.
Chemistry. 2017 Jan 18;23(4):970-975. doi: 10.1002/chem.201604855. Epub 2016 Dec 14.
We have successfully developed a series of novel and modular ferrorence-based amino-phosphine-alcohol (f-Amphol) ligands, and applied them to iridium-catalyzed asymmetric hydrogenation of various simple ketones to afford the corresponding chiral alcohols with excellent enantioselectivities and conversions (98-99.9 % ee, >99 % conversion, turnover number up to 200 000). Control experiments and density functional theory (DFT) calculations have shown that the hydroxyl group of our f-Amphol ligands played a key role in this asymmetric hydrogenation.
我们成功开发了一系列新型且模块化的基于铁的氨基膦醇(f-Amphol)配体,并将其应用于铱催化的各种简单酮的不对称氢化反应,以优异的对映选择性和转化率得到相应的手性醇(对映体过量值为98 - 99.9%,转化率> 99%,周转数高达200000)。对照实验和密度泛函理论(DFT)计算表明,我们的f-Amphol配体的羟基在该不对称氢化反应中起关键作用。