Diastereoselective synthesis of vicinal amino alcohols

Org Biomol Chem. 2012 Jun 14;10(22):4311-26. doi: 10.1039/c2ob25357g. Epub 2012 Apr 25.

Abstract

The vicinal amino alcohol is a common motif in natural products and pharmaceuticals. Amino acids constitute a natural, inexpensive, and enantiopure choice of starting material for the synthesis of such functionalities. However, the matters concerning diastereoselectivity are not obvious. This Perspective takes a look in the field of diastereoselective synthesis of vicinal amino alcohols starting from amino acids using various methods.

MeSH terms

  • Aldehydes / chemical synthesis
  • Amino Alcohols / chemical synthesis*
  • Glucosides / chemistry*
  • Molecular Structure
  • Oxidation-Reduction
  • Pyrimidinones / chemistry*
  • Stereoisomerism

Substances

  • Aldehydes
  • Amino Alcohols
  • Glucosides
  • Pyrimidinones
  • vicine