化学
差向异构体
芳基
单糖
催化作用
配体(生物化学)
铜
动力学分辨率
糖苷
偶联反应
动能
联轴节(管道)
有机化学
组合化学
立体化学
对映选择合成
生物化学
烷基
受体
机械工程
物理
量子力学
工程类
作者
Tian‐Yang Liu Hou,Yi‐Xian Li,Yue‐Mei Jia,Chu‐Yi Yu
标识
DOI:10.1002/adsc.202300997
摘要
Abstract We report a strategy for stereoselective O‐aryl‐glycoside synthesis by copper‐catalyzed cross‐coupling of a variety of anomeric sugars and (hetero)aromatic iodides. Stereocontrol of the α/β selectivity can be successfully realized by slight structural modifications of the oxalic diamide ligands. Mechanistic studies indicated a dynamic kinetic resolution (DKR) reaction mechanism controlled by the ligand structures. This reaction could be performed on gram scale, and has also been applied to the synthesis of some natural products.
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