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Synthesis and solvodynamic diameter measurements of closely related mannodendrimers for the study of multivalent carbohydrate-protein interactions. | LitMetric

Synthesis and solvodynamic diameter measurements of closely related mannodendrimers for the study of multivalent carbohydrate-protein interactions.

Beilstein J Org Chem

Pharmaqam, Department of Chemistry, Université du Québec à Montréal, P. O. Box 8888, Succ. Centre-ville, Montréal, Québec, Canada H3C 3P8.

Published: August 2014

AI Article Synopsis

  • - The paper discusses the creation of dendrimers that contain mannopyranosides to investigate how subtle structural changes affect carbohydrate-protein binding interactions.
  • - Various dendrimers were synthesized, including two trimers, three 9-mers, and one 27-mer, using a method called azide-alkyne cycloaddition (CuAAc), focusing on the distances between specific carbon atoms.
  • - The sizes of the 9-mer dendrimers were measured using a technique called pulsed-field-gradient-stimulated echo (PFG-STE) NMR, revealing diameters of 3.0, 2.5, and 3.4 nm for the different samples.

Article Abstract

This paper describes the synthesis of three closely related families of mannopyranoside-containing dendrimers for the purpose of studying subtle structural parameters involved in the measurements of multivalent carbohydrate-protein binding interactions. Toward this goal, two trimers 5 and 9, three 9-mers 12, 17, 21, and one 27-mer 23, varying by the number of atoms separating the anomeric and the core carbons, were synthesized using azide-alkyne cycloaddition (CuAAc). Compound 23 was prepared by an efficient convergent strategy. The sugar precursors consisted of either a 2-azidoethyl (3) or a prop-2-ynyl α-D-mannopyranoside (7) derivative. The solvodynamic diameters of 9-mer 12, 17, and 21 were determined by pulsed-field-gradient-stimulated echo (PFG-STE) NMR experiments and were found to be 3.0, 2.5, and 3.4 nm, respectively.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4144466PMC
http://dx.doi.org/10.3762/bjoc.10.157DOI Listing

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