Abstract
AbstractC‐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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