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离子液体在甘露糖苷化过程中的β导向性:一种具有选择性构建1,2-顺式-β-D-甘露糖连接潜力的新方法(英文)
Theβ-directing effect of ionic liquid in mannopyranosylation:a potential access to stereoselective construction of the 1,2-cis-β-D-mannopyranosyl linkage
【摘要】 首次报道了甲基咪唑型离子液体在进行6-O-乙酰基-2,3,4-O-三-苄基-甘露糖三氯乙酰业胺酯供体与离子液体载体的糖基化过程中的β导向性,并对该反应进行了深入研究,探讨了出现该现象的潜在机理。在对反应条件进行了优化之后,我们发展了一种选择性构建1,2-顺式-β-D-甘露糖连接的全新方法。
【Abstract】 We report a novel P-directing effect of imidazolium based ionic liquid,which was observed when we conducted the glycosylation of a 6-O-acetyl-2,3,4-tri-O-benzyl-mannose trichloroacetimidate donor with a modified ionic liquid support acceptor. The mechanism was investigated and a hypothesis was proposed.After optimization of the reaction conditions,an innovative method for the selective construction of 1,2-cis-β-D-mannopyranosyl linkage was developed.
【关键词】 离子液体负载策略;
糖基化;
立体选择性;
【Key words】 Ionic liquid supported strategy; Glycosylation; Stereoselectivity;
【Key words】 Ionic liquid supported strategy; Glycosylation; Stereoselectivity;
【基金】 National Natural Science Foundation of China (Grant No.20732001) ;the State New Drug Innovation(the Ministry of Science and Technology of China,Grant No. 2009ZX09501-011)
- 【文献出处】 Journal of Chinese Pharmaceutical Sciences ,中国药学(英文版) , 编辑部邮箱 ,2011年06期
- 【分类号】O636.1
- 【下载频次】69