Jump to main content
Jump to site search

Issue 23, 2009
Previous Article Next Article

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

Author affiliations

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

Back to tab navigation

Supplementary files

Article information


Submitted
23 Mar 2009
Accepted
27 Apr 2009
First published
13 May 2009

Chem. Commun., 2009, 3378-3379
Article type
Communication

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, 3378
DOI: 10.1039/B905761G

Social activity

Search articles by author

Spotlight

Advertisements