Issue 42, 2009

Direct chemoselective synthesis of glyconanoparticles from unprotected reducing glycans and glycopeptide aldehydes

Abstract

Chemoselective oxime coupling was used for facile conjugation of unprotected, reducing glycans and glycopeptide aldehydes with core–shell gold nanoparticles carrying reactive aminooxy groups on the organic shell.

Graphical abstract: Direct chemoselective synthesis of glyconanoparticles from unprotected reducing glycans and glycopeptide aldehydes

Supplementary files

Article information

Article type
Communication
Submitted
16 Jun 2009
Accepted
21 Sep 2009
First published
01 Oct 2009

Chem. Commun., 2009, 6367-6369

Direct chemoselective synthesis of glyconanoparticles from unprotected reducing glycans and glycopeptide aldehydes

M. B. Thygesen, K. K. Sørensen, E. Cló and K. J. Jensen, Chem. Commun., 2009, 6367 DOI: 10.1039/B911676A

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