Synthesis of enantiopure sugar-decorated six-armed triptycene derivatives

Synthesis of enantiopure sugar-decorated six-armed triptycene derivatives

A new class of molecules with a triptycene rigid core surrounded by six monosaccharide residues was synthesized. Hexakis(bromomethyl) substituted triptycene was converted into a six-armed triptycene azide (2,3,6,7,14,15-hexakis(azidomethyl)-9,10-dihydro-9,10-[1’,2’]benzenoanthracene). The key step o...

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Bibliographic Details
Main Authors: Paola Bonaccorsi, Maria Luisa Di Gioia, Antonella Leggio, Lucio Minuti, Teresa Papalia, Carlo Siciliano, Andrea Temperini, Anna Barattucci
Format: Article
Language:English
Published: Beilstein-Institut 2013-11-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
azide derivatives
click chemistry
glycoconjugates
2-propyn-1-yl β-D-glycopyranosides
triptycene
Online Access:https://doi.org/10.3762/bjoc.9.278

Internet

https://doi.org/10.3762/bjoc.9.278

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