Synthesis of Amino-Bridged Oligosaccharide Mimetics
✍ Scribed by Janna Neumann; Joachim Thiem
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 571 KB
- Volume
- 2010
- Category
- Article
- ISSN
- 1434-193X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Synthesis of amino‐bridged oligosaccharides using reductive amination opens rapid access to novel glycomimetic target structures as potential ligands for the receptor protein NKR P1 of natural killer cells. Emphasis was laid on fast and facile synthetic routes. The carbonyl building blocks were easily obtained by oxidation with Dess–Martin periodinane or iodoxybenzoic acid (IBX). For the required amino‐functionalized units, reduction of azide precursors was advantageous, and generation of the novel oligosaccharides was achieved by subsequent reductive amination. The target saccharide structures feature a bridging nitrogen atom inserted between two non‐anomeric positions as well as including one anomeric position.
📜 SIMILAR VOLUMES
In multivalent glycoligands including cluster glycosides, one type of sugar epitope is normally clustered. Such molecules have been valuable tools for investigation and inhibition of cell adhesion processes. They have, for example, served as in vitro antiadhesives in mannose-specific bacterial adhes