Single and dual glycoside clustering around calix[4]arene scaffolds via click Thiol-ene coupling and azide-alkyne cycloaddition

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Abstract

We present the first synthesis of calix[4]arene-based S-glycoclusters via photoinduced multiple thiol-ene coupling of tetra- and octa-allyl calix[4]arenes with peracetylated glucosyl thiol (67-88% yields). Moreover we describe the dual clustering at the upper and lower rim of a calix[4]arene with two different sugars (galactose and glucose) via sequential copper(i)-catalyzed azide-alkyne cycloaddition and photoinduced thiol-ene coupling. © 2009 The Royal Society of Chemistry.

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Fiore, M., Chambery, A., Marra, A., & Dondoni, A. (2009). Single and dual glycoside clustering around calix[4]arene scaffolds via click Thiol-ene coupling and azide-alkyne cycloaddition. Organic and Biomolecular Chemistry, 7(19), 3910–3913. https://doi.org/10.1039/b912686d

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