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      Design and Creativity in Synthesis of Multivalent Neoglycoconjugates

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          Abstract

          From the authors' opinion, this chapter constitutes a modest extension of the seminal and inspiring contribution of Stowell and Lee on neoglycoconjugates published in this series [C. P. Stowell and Y. C. Lee, Adv. Carbohydr. Chem. Biochem., 37 (1980) 225–281]. The outstanding progresses achieved since then in the field of the “glycoside cluster effect” has witnessed considerable creativity in the design and synthetic strategies toward a vast array of novel carbohydrate structures and reflects the dynamic activity in the field even since the recent chapter by the Nicotra group in this series [F. Nicotra, L. Cipolla, F. Peri, B. La Ferla, and C. Radaelli, Adv. Carbohydr. Chem. Biochem., 61 (2007) 353–398]. Beyond the more classical neoglycoproteins and glycopolymers (not covered in this work) a wide range of unprecedented and often artistically beautiful multivalent and monodisperse nanostructures, termed glycodendrimers for the first time in 1993, has been created. This chapter briefly surveys the concept of multivalency involved in carbohydrate–protein interactions. The topic is also discussed in regard to recent steps undertaken in glycobiology toward identification of lead candidates using microarrays and modern analytical tools. A systematic description of glycocluster and glycodendrimer synthesis follows, starting from the simplest architectures and ending in the most complex ones. Presentation of multivalent glycostructures of intermediate size and comprising, calix[ n]arene, porphyrin, cyclodextrin, peptide, and carbohydrate scaffolds, has also been intercalated to better appreciate the growing synthetic complexity involved. A subsection describing novel all-carbon-based glycoconjugates such as fullerenes and carbon nanotubes is inserted, followed by a promising strategy involving dendrons self-assembling around metal chelates. The chapter then ends with those glycodendrimers that have been prepared using commercially available dendrimers possessing varied functionalities, or systematically synthesized using either divergent or convergent strategies.

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            Polyvalent Interactions in Biological Systems: Implications for Design and Use of Multivalent Ligands and Inhibitors

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                Author and article information

                Journal
                Adv Carbohydr Chem Biochem
                Adv Carbohydr Chem Biochem
                Advances in Carbohydrate Chemistry and Biochemistry
                Elsevier Inc.
                0065-2318
                2162-5530
                8 April 2010
                2010
                8 April 2010
                : 63
                : 165-393
                Affiliations
                [1]Department of Chemistry, Université du Québec à Montréal, Montréal, Québec, H3C 3P8, Canada
                Article
                S0065-2318(10)63006-5
                10.1016/S0065-2318(10)63006-5
                7112031
                20381707
                f0d65a9b-5c53-4e2b-95da-8948f17da99a
                Copyright © 2010 Elsevier Inc. All rights reserved.

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                Article

                multivalency,glycoside cluster effect,protein–carbohydrate interactions,multivalent neoglycoconjugate,synthetic inhibitors,antiadhesin,click chemistry,nanostructures,carbon-based nanostructures,glyco-fullerodendrimers,glyco-nanotubes,self-assembly,glycoclusters,glycodendrons,glycodendrimers,biological investigations,ella,elisa,nephelometry,itc,hemagglutination inhibition

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