Single and dual glycoside clustering around calix[4]arene scaffolds via click thiol–ene coupling and azide–alkyne cycloaddition-Reference-Cited by-同舟云学术

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

Published:2009 Issue:19 Volume:7 Page:3910
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Fiore Michele,Chambery Angela,Marra Alberto,Dondoni Alessandro

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2009/OB/B912686D

Reference37 articles.

1. Sugar Calixarenes: Preparation of Calix[4]arenes Substituted at the Lower and Upper Rims withO-Glycosyl Groups

2. Calixsugars:† Preparation of Upper Rim O-Ketopyranosyl Calix[4]arenes

3. Synthesis and Properties ofO-Glycosyl Calix[4]Arenes (Calixsugars)

4. Glycoside-Clustering Round Calixarenes toward the Development of Multivalent Carbohydrate Ligands. Synthesis and Conformational Analysis of Calix[4]arene O- and C-Glycoconjugates

5. Synthesis of sialoclusters appended to calix[4]arene platforms via multiple azide-alkyne cycloaddition. New inhibitors of hemagglutination and cytopathic effect mediated by BK and influenza A viruses

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