Amine-Induced Deacylation of Carbohydrate Derivatives Under Anhydrous Conditions
Methanolysis of acylated carbohydrate derivatives was effectively performed using tertiary amines in the absence of water at room temperature. The reaction was performed with acetylated and benzoylated alditols, aldoses, lactones, orthoesters, glycosides, and disaccharides. N-methyl-pyrrolidine prov...
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Veröffentlicht in: | Journal of carbohydrate chemistry 1993-01, Vol.12 (1), p.13-22 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Methanolysis of acylated carbohydrate derivatives was effectively performed using tertiary amines in the absence of water at room temperature. The reaction was performed with acetylated and benzoylated alditols, aldoses, lactones, orthoesters, glycosides, and disaccharides. N-methyl-pyrrolidine proved to be especially suitable for synthetic purposes and deacylated compounds were obtained in excellent yields. The mild conditions employed and the minimum work-up needed make this method appropriate for the deacylation of labile compounds. |
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ISSN: | 0732-8303 1532-2327 |
DOI: | 10.1080/07328309308018537 |