化学
动力学分辨率
催化作用
铜
对映选择合成
组合化学
手性配体
配体(生物化学)
环加成
氨基酸
离子
分辨率(逻辑)
三唑
立体化学
点击化学
高分子化学
肽
有机化学
螯合作用
动能
光学活性
反应条件
作者
Zekai Fang,T Nie,Yu Lan,Qilong Cai,Xiaoming Wang
摘要
Copper-catalyzed azide-alkyne cycloaddition (CuAAC) is a cornerstone reaction in modern chemistry. Although binuclear catalytic mechanisms have been widely proposed and certain binuclear complexes exhibit good activity, asymmetric CuAAC still relies on the in situ assembly of copper salts with chiral ligands. Herein, guided by the postulated reaction mechanism, we employ a preassembled chiral binuclear copper catalyst with a well-defined chiral pocket to achieve efficient kinetic resolution of alkyne-functionalized azlactones with azides. This catalyst contains two copper(I) ions within a single chiral ligand framework, providing a rigid planar scaffold, stable coordination geometry, and a semicircular chiral cavity. Both triazole products and recovered azlactones are obtained in high enantiopurity and can be rapidly converted into chiral α-quaternary amino acid derivatives. This study establishes chiral binuclear copper complexes as an effective platform for enantioselective CuAAC.
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