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February 14, 2008Angewandte Chemie International Edition156 citations

From Disulfide‐ to Thioether‐Linked Glycoproteins

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GBGonçalo J. L. BernardesEGElizabeth J. GraysonSTSam Thompson

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Abstract

Strengthening the bond: The introduction of a thiol tag in combination with chemoselective ligation to form a disulfide-linked bioconjugate is a selective and useful method for site-selective protein glycosylation. The phosphine-mediated desulfurization of such glycoconjugates to their reductant-resistant thioether-linked counterparts completes a convergent, site-selective synthesis of thioether-linked glycoproteins (see scheme). Supporting information for this article is available on the WWW under http: //www. wiley-vch. de/contents/jc₂002/2008/z704381ₛ. pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

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Cite This Study

Bernardes et al. (2008) studied this question.

synapsesocial.com/papers/69dcc3bcf3d3790cb7133b0chttps://doi.org/10.1002/anie.200704381
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