吲哚试验
碘
色氨酸
催化作用
化学
组合化学
有机化学
生物化学
氨基酸
作者
Jie Huang,Fenglian Wei,Bin Wu,Wen‐Wu Sun
标识
DOI:10.1021/acs.joc.5c01715
摘要
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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