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Click Glycodendrimers Containing 27, 81, and 243 Modified Xylopyranoside Termini

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 74, Issue 14, Pages 5071-5074

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo900554b

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Funding

  1. Universities Bordeaux I and Reims Champagne-Ardenne
  2. Centre National de la Recherche Scientifique (CNRS)
  3. Institut Universitaire de France
  4. Contrats d'objectifs in Europol'Agro framework (Glycoval program)
  5. Ministere de la Recherche et de la Technologie

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A series of large glycodendrimers containing 27, 81, and 243 terminal modified xylose branches from the first (G(1)-27) to the third generation (G(3)-243) were synthesized from 2'-azidoethyl 2,3,4-tri-O-acetyl-beta-D-xylopyranoside and alkynyl-terminated dendrimers by click chemistry that is confirmed to be an excellent method to obtain large glyco-dendtimers exemplified by the use of modified xylose. The dendrimers were first characterized by H-1 NMR, C-13{H-1} NMR, elemental analysis, and IR spectroscopy. The size progression in the series was also demonstrated using both DOSY NMR and size exclusion chromatography (SEC), the latter technique showing the good polydispersity of all the dendrimers. The size measured by dynamic light scattering (DLS) for the dendrimer G(3)-243 is close to that obtained by the DOSY NMR method.

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