Publications by authors named "David Antal"

Article Synopsis
  • - The study investigates how O-peracetylated and O-perbenzoylated glycals with different substituents react with various nucleophiles in the presence of Lewis acids.
  • - Specific nucleophiles, such as simple alcohols and chloride ions, led to the formation of allylic substituted products with distinct axial stereoselectivity.
  • - Interestingly, when benzyl thiol was used, a rearrangement occurred, producing thioglycosides, and a sugar-derived thiol generated both allylic substituted and rearranged products.
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