立体中心
铱
催化作用
化学
硼
三氟甲基
不对称氢化
有机化学
高分子化学
对映选择合成
药物化学
烷基
作者
Marcus G. Schrems,Eva Neumann,Andreas Pfaltz
标识
DOI:10.1002/anie.200702555
摘要
Even notoriously unreactive substrates such as tetrasubstituted unfunctionalized olefins can be hydrogenated with high efficiency and excellent enantioselectivity using readily accessible chiral Ir catalysts. In this way, two adjacent stereogenic centers can be introduced in a single step (see scheme for an example; BArF=tetrakis(3,5-di(trifluoromethyl)phenyl)borate, o-Tol=ortho-tolyl).
科研通智能强力驱动
Strongly Powered by AbleSci AI