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Issue 23, 2009
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One-step conversion of unprotected sugars to β-glycosyl azides using 2-chloroimidazolinium salt in aqueous solution

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Abstract

Various β-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).

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

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Publication details

The article was received on 23 Mar 2009, accepted on 27 Apr 2009 and first published on 13 May 2009


Article type: Communication
DOI: 10.1039/B905761G
Citation: Chem. Commun., 2009,0, 3378-3379
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    One-step conversion of unprotected sugars to β-glycosyl azides using 2-chloroimidazolinium salt in aqueous solution

    T. Tanaka, H. Nagai, M. Noguchi, A. Kobayashi and S. Shoda, Chem. Commun., 2009, 0, 3378
    DOI: 10.1039/B905761G

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