化学
糖基化
芳基
催化作用
糖苷
立体选择性
钌
组合化学
立体化学
有机化学
生物化学
烷基
作者
Wei‐Yu Shi,H.-L. Li,Xue‐Ya Gou,Yu‐Yong Luan,Nian Zheng,Zhi‐Jie Niu,Zhe Zhang,Xue‐Yuan Liu,Yong‐Min Liang
标识
DOI:10.1002/adsc.202200549
摘要
Abstract C ‐Aryl glycoside is a class of structural motifs with important medicinal value. Herein, a remote C−H glycosylation strategy enabled by Ruthenium(II)‐catalyzed with mostly α‐stereoselectivity is described. This approach exhibits great functional group compatibility with various glycosides and arylamides. A series of experiments provided strong evidence for the free radical mechanism and reversible C−H activation process, and a possible mechanism was proposed. magnified image
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