Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1389975 | Carbohydrate Research | 2006 | 12 Pages |
Abstract
Selective and per-O-acylation of carbohydrate derivatives using acyl chlorides and Al2O3, a solid support reagent, is reported. This protocol does not require the addition of any base or activator. This methodology has been further extended to the selective acylation of carbohydrate diols and the one-pot preparation of acetylated glycosyl chlorides direct from free reducing sugars. The yields obtained in most of the cases are excellent.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Pallavi Tiwari, Anup Kumar Misra,