Dale et al. discussed the role of the hydroxyl groups in the interaction of sugars with the /3-glucosidase by investigating the inhibitory effects of some monosaccharides and their derivatives against the enzyme [1]. We planned to investigate the role of glycon hydroxyl groups via a kinetic study on
Synthesis of 6-Deoxy and 3,6-Dideoxy Derivatives from Unprotected Glycosides Employing the Mitsunobu Reaction
β Scribed by Dancy, Isabelle ;Laupichler, Lothar ;Rollin, Patrick ;Thiem, Joachim
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 861 KB
- Volume
- 1993
- Category
- Article
- ISSN
- 0947-3440
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β¦ Synopsis
Abstract
Starting with unprotected hexopyranoside derivatives, an efficient synthesis of 6βdeoxyβ and 3,6βdideoxyhexopyranosides was achieved in two consecutive steps involving a highly regioselective Mitsunobu reaction and subsequent desulfurization.
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The following compounds have been prepared for use as glycosyl donors: 1