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Palladium-Catalyzed O -Glycosylation through π-π Interactions.

Yangxing SunKeke RenZhentao ZhangYanzhi LiNengzhong WangHui ZengNianyu HuangXiao-Xi LiWei-Qiao DengHui Yao
Published in: Organic letters (2024)
A stereodivergent synthesis of β- and α- O -glycosides using 3- O -quinaldoyl glucals was developed by palladium catalysis at 60 and 110 °C respectively. Various alcohols, monosaccharides, and amino acid were glycosylated to form β- and α- products in good yields with high stereoselectivity. Mechanistic studies indicated no classic Pd-N (quinoline) coordination, but π-π stacking interactions promoted the anomeric stereodiversity. The practicality was demonstrated by glycosylating natural products/drugs and synthesizing a complex tetrasaccharide.
Keyphrases
  • amino acid
  • molecular docking
  • reduced graphene oxide
  • gold nanoparticles
  • visible light