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Stereoselective Synthesis of 2-Deoxythiosugars from Glycals.

Xueying YouYifei CaiChenyu XiaoLijuan MaYong WeiTianpeng XieLei ChenHui Yao
Published in: Molecules (Basel, Switzerland) (2022)
2-deoxythiosugars are more stable than 2-deoxysugars occurring broadly in bioactive natural products and pharmaceutical agents. An effective and direct methodology to stereoselectively synthesize α-2-deoxythioglycosides catalyzed by AgOTf has been developed. Various alkyl thiols and thiophenols were explored and the desired products were formed in good yields with excellent α-selectivity. This method was further applied to the syntheses of S -linked disaccharides and late-stage 2-deoxyglycosylation of estrogen, L-menthol, and zingerone thiols successfully.
Keyphrases
  • ionic liquid
  • room temperature
  • fluorescent probe
  • estrogen receptor
  • visible light