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Issue 42, 2009
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Direct chemoselective synthesis of glyconanoparticles from unprotected reducing glycans and glycopeptide aldehydes

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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

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Publication details

The article was received on 16 Jun 2009, accepted on 21 Sep 2009 and first published on 01 Oct 2009


Article type: Communication
DOI: 10.1039/B911676A
Citation: Chem. Commun., 2009,0, 6367-6369

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    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, 0, 6367
    DOI: 10.1039/B911676A

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