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Macro-Glycoligands

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Cover of 'Macro-Glycoligands'

Table of Contents

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    Book Overview
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    Chapter 1 Synthesis of Chain-End Functionalized Glycopolymers via Cyanoxyl-Mediated Free Radical Polymerization (CMFRP)
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    Chapter 2 Protecting-Group-Free Synthesis of Well-Defined Glycopolymers Featuring Negatively Charged Oligosaccharides
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    Chapter 3 Glycopolymers Prepared by Ring-Opening Metathesis Polymerization Followed by Glycoconjugation Using a Triazole-Forming “Click” Reaction
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    Chapter 4 Protecting-Group-Free Synthesis of Glycopolymers and Their Binding Assay with Lectin and Influenza Virus
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    Chapter 5 Carbohydrate-Based Initiators for the Cationic Ring-Opening Polymerization of 2-Ethyl-2-Oxazoline
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    Chapter 6 Heterofunctional Glycopolypeptides by Combination of Thiol-Ene Chemistry and NCA Polymerization
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    Chapter 7 Preparation of Proteoglycan Mimetic Graft Copolymers
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    Chapter 8 Galactosylated Polymer Nano-objects by Polymerization-Induced Self-Assembly, Potential Drug Nanocarriers.
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    Chapter 9 Synthetic Approach to Biotinylated Glyco-Functionalized Quantum Dots: A New Fluorescent Probes for Biomedical Applications
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    Chapter 10 Surface Modification of Polydivinylbenzene Microspheres with a Fluorinated Glycopolymer Using Thiol-Halogen Click Chemistry
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    Chapter 11 Glycopolymer-Grafted Polymer Particles for Lectin Recognition
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    Chapter 12 Synthesis of Non-spherical Glycopolymer-Decorated Nanoparticles: Combing Thiol-ene with Catecholic Chemistry
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    Chapter 13 Synthetic Approach to Glycopolymer Base Nanoparticle Gold(I) Conjugate: A New Generation of Therapeutic Agents
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    Chapter 14 Multivalent Glycopolymer-Coated Gold Nanoparticles
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    Chapter 15 Modulation of Multivalent Protein Binding on Surfaces by Glycopolymer Brush Chemistry
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    Chapter 16 Oriented Immobilized Sialyloligo-macroligand Microarray
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    Chapter 17 Glycocalyx Remodeling with Glycopolymer-Based Proteoglycan Mimetics
Attention for Chapter 2: Protecting-Group-Free Synthesis of Well-Defined Glycopolymers Featuring Negatively Charged Oligosaccharides
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Chapter title
Protecting-Group-Free Synthesis of Well-Defined Glycopolymers Featuring Negatively Charged Oligosaccharides
Chapter number 2
Book title
Macro-Glycoligands
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3130-9_2
Pubmed ID
Book ISBNs
978-1-4939-3129-3, 978-1-4939-3130-9
Authors

Luca Albertin

Abstract

Control of the macromolecular architecture is essential to enable sophisticated functions for glycopolymers and to allow a precise correlation between these functions and the polymer structure. A number of biologically important ligands are negatively charged oligosaccharides that are difficult to manipulate in organic solvent and that are hardly amenable to protection/deprotection strategies. RAFT polymerization is a simple and robust technique that enables the synthesis of well-defined glycopolymers directly in aqueous solution and starting from unprotected vinyl glycomonomers. Here I describe how RAFT polymerization can be combined with reductive amination to transform negatively charged oligosaccharides having 5-20 monosaccharide units into well-defined glycopolymers directly in water and without the need to resort to protecting-group chemistry.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 2 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 2 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 50%
Researcher 1 50%
Readers by discipline Count As %
Chemical Engineering 1 50%
Chemistry 1 50%