Using click chemistry to access mono- and ditopic β-cyclodextrin hosts substituted by chiral amino acids. - Université de Rennes Accéder directement au contenu
Article Dans Une Revue Carbohydrate Research Année : 2011

Using click chemistry to access mono- and ditopic β-cyclodextrin hosts substituted by chiral amino acids.

Diem Ngan Tran
  • Fonction : Auteur
  • PersonId : 767288
  • IdRef : 13495369X
Claire Blaszkiewicz
  • Fonction : Auteur
Karine Philippot
Eric Monflier

Résumé

A wide range of chiral mono- and ditopic cyclodextrin-based receptors have been synthesized by CuI-catalyzed azide-alkyne cycloaddition starting from mono-6-azido-β-cyclodextrin and chiral amino acids. Of interest, microwaves proved very efficient to access a wide range of ditopic β-cyclodextrin receptors with quantitative yields.

Domaines

Chimie organique

Dates et versions

hal-00753314 , version 1 (19-11-2012)

Identifiants

Citer

Diem Ngan Tran, Claire Blaszkiewicz, Stéphane Menuel, Alain Roucoux, Karine Philippot, et al.. Using click chemistry to access mono- and ditopic β-cyclodextrin hosts substituted by chiral amino acids.. Carbohydrate Research, 2011, 346 (2), pp.210-8. ⟨10.1016/j.carres.2010.11.024⟩. ⟨hal-00753314⟩
175 Consultations
0 Téléchargements

Altmetric

Partager

Gmail Facebook X LinkedIn More