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    Reaction of Glyconitriles with Organometallic Reagents: Access to Acyl β‑<i>C</i>‑Glycosides

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    A new strategy for the synthesis of acyl β-<i>C</i>-glycosides is described. The reactivity of glyconitriles toward organometallic reagents such as organomagnesium or organolithium derivatives was studied, affording acyl β-<i>C</i>-glycosides in moderate to good yields. In this study, glycal formation was efficiently prevented by deprotonating the hydroxyl group in position 2 of the glyconitriles during the process
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