Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5272512 | Tetrahedron Letters | 2010 | 6 Pages |
Abstract
6,5-Fused sugar-derived spiroaminals have been synthesized from the azido esters obtained via the nucleophilic substitution reactions of unstable Michael adducts derived from 1-nitro sugars. Most of the spiroaminals synthesized showed moderate but selective inhibitory activities toward some glycosidases.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
A.P. John Pal, Yashwant D. Vankar,