化学
位阻效应
不对称氢化
组合化学
催化作用
还原消去
可扩展性
对映体
计算化学
配体(生物化学)
对映体过量
对映选择合成
密度泛函理论
桥接(联网)
计算
催化加氢
有机化学
过程(计算)
非共价相互作用
立体异构
化学选择性
均相催化
串联
作者
Hao Wang,Longxue Xiang,Yu Chen,Xu Tang,Jiahui Wu,Longsheng Zheng,Xiuxiu Li,Peiyuan Yu,Zhenghui Guan,Xumu Zhang
摘要
Herein, we report a simple, one-pot, scalable process for the preparation of a series of enamides, which were subsequently hydrogenated with high efficiency and excellent enantioselectivity to the corresponding chiral amides using the Rh-ZhangPhos catalyst. This methodology is practical and facilitates easy postreaction handling, with the hydrogenation providing nearly perfect stereoselectivity. DFT studies uncovered distinct rate-determining steps for competing enantiomeric pathways: migrational insertion for the major product and reductive elimination for the minor product, challenging conventional assumptions of a unified mechanistic origin. Noncovalent interaction analysis, particularly steric repulsion in the reductive elimination step, offers a theoretical rationale for long-standing empirical strategies in bisphosphine ligand design, bridging experiment, and computation in asymmetric hydrogenation.
科研通智能强力驱动
Strongly Powered by AbleSci AI