化学
选择性
取代基
密度泛函理论
非共价相互作用
磷酸
计算化学
刚度(电磁)
立体化学
蛋白质-蛋白质相互作用
分子间力
分子
组合化学
立体异构
分子间相互作用
氨基酸
聚合物
分子构象
作者
Ran Zhang,Zihao Li,Shu‐Yu Zhang,Abing Duan
标识
DOI:10.1021/acs.orglett.6c03162
摘要
Abstract Chiral phosphoric acids (CPAs) can regulate reaction selectivity via catalyst–substrate noncovalent interactions (NCIs). Most studies remain macroscopic and have not addressed how CPA structures modulate the interaction strength and thereby selectivity. This study reveals that, in CPA-catalyzed N-hydroxyalkylation reactions, the CPA backbone rigidity and substituent structure promote stronger interactions, thereby enhancing enantioselectivity. An ordered π system facilitates the formation of more pronounced π–π stacking.
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