Abstract
Pentose
and hexose sugars are abundant constituents of waste biomass, making them
sustainable, chiral building blocks for organic synthesis. The demand for
chiral saturated heterocyclic rings from the pharmaceutical industry is
increasing as they provide well-defined three-dimensional frameworks that show
increased metabolic resistance. Through the formation of thioacetals, sugars may
be manipulated in their straight-chain form and dehydrated selectively under
basic conditions at C-2. This approach was applied to an array of sugars and
extended to the production of useful chiral THFs via further selective
dehydration reactions.
Supplementary materials
Title
ThioacetalChemrxivSI
Description
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