Synthesis of Amino-Bridged Oligosaccharide Mimetics

被引:13
|
作者
Neumann, Janna [1 ]
Thiem, Joachim [1 ]
机构
[1] Univ Hamburg, Fac Sci, Dept Chem, D-20146 Hamburg, Germany
关键词
Carbohydrate mimetics; Reductive amination; Oxidation; Oligosaccharides; Bridging ligands; Natural killer cell; IODOXYBENZOIC ACID IBX; CARBOHYDRATE-RECOGNITION; DERIVATIVES; ACTIVATION; ALCOHOLS; LIGANDS; ANTIGEN; NKR-P1; CELLS;
D O I
10.1002/ejoc.200901106
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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.
引用
收藏
页码:900 / 908
页数:9
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