Chiral reagents in glycosylation and modification of carbohydrates

Chem Soc Rev. 2018 Feb 5;47(3):681-701. doi: 10.1039/c7cs00432j.

Abstract

Carbohydrates play a significant role in numerous biological events, and the chemical synthesis of carbohydrates is vital for further studies to understand their various biological functions. Due to the structural complexity of carbohydrates, the stereoselective formation of glycosidic linkages and the site-selective modification of hydroxyl groups are very challenging and at the same time extremely important. In recent years, the rapid development of chiral reagents including both chiral auxiliaries and chiral catalysts has significantly improved the stereoselectivity for glycosylation reactions and the site-selectivity for the modification of carbohydrates. These new tools will greatly facilitate the efficient synthesis of oligosaccharides, polysaccharides, and glycoconjugates. In this tutorial review, we will summarize these advances and highlight the most recent examples.

Publication types

  • Review

MeSH terms

  • Carbohydrates / chemistry*
  • Glycosylation
  • Molecular Conformation
  • Stereoisomerism

Substances

  • Carbohydrates