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When cyclodextrins meet click chemistry

Year: 2012

Journal: European Journal of Organic Chemistry Issue 22, August 2012, Pages 4087-4105, 20120922

Authors: Faugeras, P.-A.ab, Boëns, B.a, Elchinger, P.-H.ab, Brouillette, F.b, Montplaisir, D.b, Zerrouki, R.b, Lucas, R.c

Last authors: Lucas, R

Organizations: a Laboratoire de Chimie des Substances Naturelles, EA1069, 123 Avenue Albert Thomas, 87060 Limoges, France b Centre de Recherche sur les Matériaux Lignocellulosiques, Université du Québec à Trois-Rivières, 3351 boul. des Forges, Trois-Rivières, QC G9A 5H7, Canada c Laboratoire Science des Procédés Céramiques et de Traitements de Surface, UMR CNRS 6638, 12 Rue Atlantis, 87068 Limoges, France

Country: France, Canada

Cyclodextrins are important building blocks in organic chemistry. This review deals with the role of click chemistry in this family of cyclic oligosaccharides, focusing on the different areas of chemistry, including chromatography, biological applications, the elaboration of superstructures, and metal detection, that benefit from this reaction. In this paper, attention is given to organic modifications by using functionalizations such as azidation and propargylation and to click chemistry grafting onto the two faces of cyclodextrins. Research papers where cyclodextrins are not directly involved in a click chemistry reaction are not considered. A summary of chemical advances in the fields of chromatography, biological applications, the elaboration of superstructures, and metal detection is given when cyclodextrins meet the copper-catalyzed azide-alkyne cycloaddition reaction.