In this communication, our attention will be focused on the accomplishment of a synthetic patway based on the efficient azide/alkynes 1,3-dipolar cycloaddition for obtaining molecules showing a rigid lipophilic core represented by the triptycene skeleton that is linked, by the arene rings, to six sugar moieties, through six triazole units as spacers.

Synthesis of Enantiopure Sugar-Decorated Triptycene Derivatives

MINUTI, Lucio;TEMPERINI, Andrea;
2014

Abstract

In this communication, our attention will be focused on the accomplishment of a synthetic patway based on the efficient azide/alkynes 1,3-dipolar cycloaddition for obtaining molecules showing a rigid lipophilic core represented by the triptycene skeleton that is linked, by the arene rings, to six sugar moieties, through six triazole units as spacers.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11391/1296500
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