4.7 Article

Photoredox-catalyzed protecting-group-free C-glycosylation with glycosyl sulfinate via the Giese reaction

Journal

CHEMICAL COMMUNICATIONS
Volume 59, Issue 55, Pages 8564-8567

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3cc02361c

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In this study, a protection-group-free and photoredox-catalyzed C-glycosylation method using glycosyl sulfinates and Michael acceptors via the Giese radical addition is reported. This method provides a useful tool for synthesizing C-glycoside analogs of naturally occurring glycoconjugates in chemical biology studies.
C-Glycoside analogs of naturally occurring glycoconjugates are useful tools for chemical biology studies, but their synthesis usually requires protection of the hydroxyl groups of the glycosyl donors. Here we report protecting-group-free and photoredox-catalyzed C-glycosylation with glycosyl sulfinates and Michael acceptors via the Giese radical addition.

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