About this item
- Title
- Synthesis of Neoglycopeptides via Click Chemistry
- Content partner
- The University of Auckland Library
- Collection
- ResearchSpace@Auckland
- Description
Novel chemical methods to access homogeneous samples of glycopeptides and glycoproteins and their mimetics, so-called neoglycopeptides and neoglycoproteins, have developed rapidly in recent years owing to an increased need to investigate both their roles in molecular biology and their potential as therapeutic agents. This article summarizes the application of the copper-catalyzed azide-alkyne cycloaddition for the chemical synthesis of neoglycopeptides and neoglycoproteins.
- Format
- Research paper
- Research format
- Journal article
- Date created
- 2010
- Creator
- Miller, N / Williams, Geoffrey / Brimble, Margaret
- URL
- http://hdl.handle.net/2292/7986
- Related subjects
- Neoglycopeptides / Neoglycoproteins / Glycosylation / Conjugation / Azide-alkyne cycloadditon / Click chemistry / AZIDE-ALKYNE CYCLOADDITION / GLCNAC-MODIFIED PROTEINS / T-CELL EPITOPE / 1,3-DIPOLAR CYCLOADDITION / GLYCOPEPTIDE ANTIGENS / TERMINAL ALKYNES / DERIVATIVES / VACCINES / CONSTRUCTION / INDUCTION
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