Addressing the scope of the azide-nitrile cycloaddition in glycoconjugate chemistry. The assembly of C-glycoclusters on a calix[4] arene scaffold through tetrazole spacers

Alessandro Dondoni; Alberto Marra

doi:10.1016/j.tet.2007.03.045

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Addressing the scope of the azide-nitrile cycloaddition in glycoconjugate chemistry. The assembly of C-glycoclusters on a calix[4] arene scaffold through tetrazole spacers

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Addressing the scope of the azide-nitrile cycloaddition in glycoconjugate chemistry. The assembly of C-glycoclusters on a calix[4] arene scaffold through tetrazole spacers

Alessandro Dondoni et Alberto Marra

Tetrahedron, Vol.63(27), pp.6339-6345

02/07/2007

DOI: https://doi.org/10.1016/j.tet.2007.03.045

Résumé

Chemistry

Chemistry, Organic

Physical Sciences

Science & Technology

New glycoclusters constituted of ribosylmethyl, galactosylmethyl, and glucosylmethyl fragments assembled on a calix[ 4] arene platform by means of propoxytetrazole spacers have been prepared by coupling the corresponding sugar azides with p-toluenesulfonyl cyanide, and then reacting 1-glycosylmethyl-5-sulfonyl-tetrazole derivatives thus formed with a calix[ 4] arene tetrol. (c) 2007 Elsevier Ltd. All rights reserved.

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Détails

Titre: Addressing the scope of the azide-nitrile cycloaddition in glycoconjugate chemistry. The assembly of C-glycoclusters on a calix[4] arene scaffold through tetrazole spacers
Créateurs - sans rôle: Alessandro Dondoni - University of Ferrara
Alberto Marra - Univ Ferrara, Chim Organ Lab, Dipartimento Chim, I-44100 Ferrara, Italy
Détails de publication: Tetrahedron, Vol.63(27), pp.6339-6345
Éditeur: Elsevier
Nombre de pages: 7
Identifiants: 99163058809311
Unité académique: Institut des Biomolécules Max Mousseron - IBMM
Langue: English
Type de ressource: Journal article