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Organocatalytic atroposelective synthesis of naphthoquinone thioglycosides from aryl-naphthoquinones and thiosugars.

Yuling WuWu-Jingyun ZhouLaiping YaoYadi NiuHongli ZhaoCheng PengBo HanWei HuangGu Zhan
Published in: Chemical communications (Cambridge, England) (2023)
In this study, we report an organocatalytic formal coupling strategy for aryl-naphthoquinones with thiosugars that provides straightforward access to the axially chiral naphthoquinone thioglycoside with excellent stereoselectivity. Mechanistic studies revealed the key role of H-bonding in stereochemical recognition. The reaction pathway involves the atroposelective addition, followed by stereoretentive oxidation of the hydroquinone intermediate.
Keyphrases
  • electron transfer
  • room temperature
  • mass spectrometry
  • visible light