Iodine-catalyzed thioglycosylation yields up to 97% of thioglycosides in peptides, suggesting a new pathway for glycochemistry applications.
An efficient iodine-catalyzed thioglycosylation reaction for the synthesis of indole thioglycosides and S-glycosylated peptides is reported. This method employs molecular iodine as a metal-free catalyst and thioglycosides as sulfur donors, achieving high yields (up to 97%) under mild conditions. The reaction is compatible with a broad range of substrates, including various monosaccharide-derived thioglycosides and indoles with different substituents. Additionally, the method is successfully applied to the functionalization of tryptophan-containing peptides, yielding thioglycopeptide derivatives in moderate to good yields. The study not only expands the synthetic accessibility to S-linked glycopeptides but also provides a valuable approach for peptide functionalization in glycochemistry.
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Huang et al. (2025) studied this question.
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