Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5286622 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Glycosylation of a variety of alcohols with 3,4,6-tri-O-acetyl-2-N-dimethylphosphoryl-2-deoxy-α-d-glucopyranosyl trichloroacetimidate as a glycosyl donor provided the corresponding coupled products in high yields and good β-selectivity. N-Dimethylphosphoryl-protection stayed stable under acidic and basic conditions for further elaboration of the glucosamine-containing oligosaccharides.
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Authors
You Yang, Biao Yu,