Ni-Catalyzed and Pentafluorobenzoate-Leaving-Group-Enabled Stereoselective C-Aryl Glycosylation
Weilong Wu1, Yiliang Zhang1,2, Bingxin Li1,2
1College of Chemistry and Chemical Engineering and Luoyang Key Laboratory of Green Synthesis and Photofunctional Materials, Luoyang Normal University, Luoyang, Henan 471934, China.
Abstract:
Inspired by the excellent stereoinduction of palladium catalytic glycosylation with glycals via an inner-sphere pathway, a nickel-catalyzed, stereoselective C-aryl glycosylation has been developed for glucals bearing a pentafluorobenzoate (PFB) group at the C3 position. The extremely electron-deficient nature of PFB not only endows stronger activity compared to the traditional leaving groups but also functions as an orientation group, presumably through the strong π-π interactions with the bipyridine ligand coordinated to the nickel center, thereby enabling the β-selective formation of a C-aryl glycosidic bond with aryl iodides as glycosyl acceptors under mild conditions. This method features a broad substrate scope, high efficiency, and scalability, providing a general solution to the synthesis of challenging β-C-glycosides.
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