| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1386094 | Carbohydrate Research | 2006 | 7 Pages |
Abstract
Conditions of the butadiene telomerization with benzylated aldoses with a free anomeric hydroxyl, which efficiently furnish the corresponding octadienyl compounds have been determined. Deprotection and hydrogenation of the telomers over Pd/C led to the octyl glycosides.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Alla Bessmertnykh, Françoise Hénin, Anna Serra-Muns, Jacques Muzart, Henri Baillia,