Abstract
AbstractAn efficient glycosylation method to synthesize 2‐deoxy‐C‐aryl glycosides was developed. This C‐glycosylation strategy is based on a palladium‐catalyzed desulfitative Ferrier‐type coupling reaction of glycals and sodium arylsulfinates. A series of C‐aryl glycosides were obtained in moderate to good yields with exclusive regio‐ and stereoselectivities. The anomeric selectivity was found to depend on the configuration of the C3 substituent of the glycals.
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