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Issue 1, 2013
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A general and convergent synthesis of diverse glycosylphosphatidylinositol glycolipids

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Abstract

Glycosylphosphatidylinositol (GPI) glycolipids anchor a large number of proteins in the cell membrane of eukaryotic cells. Their conserved pseudopentasaccharide core carries additional phosphoethanolamine, saccharide and lipid substituents. These structural variations are characteristic for a species or a tissue but their functional significance remains largely unknown. Studies that would link a specific function to a structurally unique GPI rely on availability of homogeneous samples of these glycolipids. To address this need we have developed a general synthetic route to GPI glycolipids. Our convergent synthesis starts from common building blocks and relies on a fully orthogonal set of protecting groups that enables the regioselective introduction of phosphodiesters and efficient assembly of the GPI glycans. Here, we report on the development of this synthetic strategy, evaluation of the set of protecting groups with respect to phosphorylation methods, evaluation of the assembly plan for the GPI glycan, optimization of the glycosylation reactions, and the application of this strategy to the total syntheses of four structurally diverse branched GPI glycolipids.

Graphical abstract: A general and convergent synthesis of diverse glycosylphosphatidylinositol glycolipids

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Publication details

The article was received on 12 Sep 2012, accepted on 12 Oct 2012 and first published on 01 Nov 2012


Article type: Edge Article
DOI: 10.1039/C2SC21515B
Citation: Chem. Sci., 2013,4, 468-481
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    A general and convergent synthesis of diverse glycosylphosphatidylinositol glycolipids

    Y. Tsai, S. Götze, I. Vilotijevic, M. Grube, D. V. Silva and P. H. Seeberger, Chem. Sci., 2013, 4, 468
    DOI: 10.1039/C2SC21515B

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