对映选择合成
酮
二茂铁
化学
配体(生物化学)
部分
恶唑啉
组合化学
催化作用
有机化学
立体化学
受体
电极
电化学
生物化学
物理化学
作者
Jianfei Yu,Fanping Huang,Fang Wei,Congcong Yin,Chuan Shi,Qiwei Lang,Gen‐Qiang Chen,Xumu Zhang
标识
DOI:10.1016/j.gresc.2022.03.004
摘要
The development of highly active and enantioselective ligands and catalysts for the asymmetric hydrogenation of ketone has been the goal of synthetic chemists for more than fifty years. Herein, a series of ferrocene-based tetradentate ligands were developed and applied in Ir-catalysed asymmetric hydrogenation of ketone. The hydrolytic ring-opening of the oxazoline moiety of ligand f-amphox leads to the accidental discovery of a highly efficient and enantioselective tetradentate ligand f-phamidol which showed extraordinarily high reactivity and enantioselectivity (up to 99% yield, up to >99% ee and up to 1,000,000 TON). In addition, two types of other tetradentate ligands f-phamida and f-phamide were also synthesized and evaluated.
科研通智能强力驱动
Strongly Powered by AbleSci AI