Aniline-catalyzed reductive amination as a powerful method for the preparation of reducing end-"clickable" chitooligosaccharides

Bioconjug Chem. 2013 Apr 17;24(4):544-9. doi: 10.1021/bc3003716. Epub 2013 Mar 22.

Abstract

Functionalized oligosaccharides are useful intermediates to prepare products for biological research or for the development of advanced functional materials. Here, we report the unprecedented use of aniline as an efficient organocatalyst reaction with "clickable" (azide or alkyne) amine for the transimination-mediated reductive amination of a chitooligosaccharide. Moreover, we demonstrate that alkyne-bearing aniline constitutes an excellent tool for the easy derivatization of chitosan oligosaccharides. Evidence for such improvement has been illustrated by the straightforward design of a FRET substrate to probe chitinase activity and of amphiphilic polycaprolactone-grafted-chitosan. This efficient methodology paves the way to the preparation of novel chitosan oligosaccharide-based advanced materials.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amination
  • Aniline Compounds / chemistry*
  • Carbohydrate Conformation
  • Catalysis
  • Click Chemistry*
  • Molecular Sequence Data
  • Oligosaccharides / chemical synthesis*
  • Oligosaccharides / chemistry
  • Oxidation-Reduction

Substances

  • Aniline Compounds
  • Oligosaccharides
  • aniline