Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1367972 | Bioorganic & Medicinal Chemistry Letters | 2005 | 4 Pages |
Abstract
1-Glycosyl-4-phenyl triazoles have been prepared via a copper-mediated [3 + 2] cycloaddition of glycosyl azides with phenylacetylene. These triazoles have been evaluated for their ability to inhibit the enzymatic activity of glycosidases.
Graphical abstractGlycosyl triazoles have been prepared by a ‘click’ reaction between glycosyl azides and alkynes. These triazoles are inhibitors of β-galactosidases from Escherichia coli and bovine liver.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Lauren L. Rossi, Amit Basu,