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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Stereoselective synthesis of a novel Galf-disaccharide mimic: β-D-galactofuranosyl-(l-5)-β-D-galactofuranosyl motif of mycobacterial cell walls
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Stereoselective synthesis of a novel Galf-disaccharide mimic: β-D-galactofuranosyl-(l-5)-β-D-galactofuranosyl motif of mycobacterial cell walls

机译:立体选择性合成新型Galf-二糖模拟物:分枝杆菌细胞壁的β-D-半乳糖呋喃糖基-(l-5)-β-D-半呋喃糖醇基序

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摘要

A Galf-disaccharide mimic, an analogue of the acceptor substrates of mycobacterial Gal/-transferases, was obtained by nucleophilic addition of a L-arabinofurano-alkyne to iminogalactitol-derived nitrone. Remarkably, the nucleophilic addition could be performed highly efficiently and stereoselectively in the presence of diethylzinc in toluene using protected nitrone and alkynyl sugar as reaction partners and thus opens a concise approach to a diversity of disaccharide mimics.
机译:Galf-二糖模拟物是分枝杆菌Gal /-转移酶受体底物的类似物,是通过将L-阿拉伯呋喃糖炔基向亚氨基半乳糖醇衍生的腈亲核加成而获得的。值得注意的是,亲核加成反应可以在甲苯中存在二乙基锌的情况下,使用受保护的硝酮和炔基糖作为反应伙伴,高效而立体地进行,从而为多种二糖模拟物提供了一种简洁的方法。

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