One-step conversion of unprotected sugars to β-glycosyl azides using 2-chloroimidazolinium salt in aqueous solution

One-step conversion of unprotected sugars to β-glycosyl azides using 2-chloroimidazolinium salt in aqueous solution
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DOI:
10.1039/b905761g
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发表时间:
2009-01-01
影响因子:
4.9
通讯作者:
Shoda, Shin-ichiro
Shoda, Shin-ichiro
中科院分区:
化学2区
文献类型:
--
作者:
Tanaka, Tomonari;Nagai, Hikaru;Shoda, Shin-ichiro

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在2-氯-1,3-二甲基咪唑鎓氯化物(DMC)的作用下,无保护的糖与叠氮化钠反应,在水中直接合成了多种β-糖基叠氮化合物。
Various beta-glycosyl azides have been synthesized directly in water by the reaction of unprotected sugars and sodium azide mediated by 2-chloro-1,3-dimethylimidazolinium chloride (DMC).