Direct chemoselective synthesis of glyconanoparticles from unprotected reducing glycans and glycopeptide aldehydes
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Direct chemoselective synthesis of glyconanoparticles from unprotected reducing glycans and glycopeptide aldehydes. / Thygesen, Mikkel Boas; Sørensen, Kasper Kildegaard; Cló, Emiliano; Jensen, Knud Jørgen.
In: Chemical Communications, No. 42, 11.2009, p. 6367-9.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Direct chemoselective synthesis of glyconanoparticles from unprotected reducing glycans and glycopeptide aldehydes
AU - Thygesen, Mikkel Boas
AU - Sørensen, Kasper Kildegaard
AU - Cló, Emiliano
AU - Jensen, Knud Jørgen
PY - 2009/11
Y1 - 2009/11
N2 - 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.
AB - 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.
KW - Aldehydes
KW - Glycopeptides
KW - Gold
KW - Metal Nanoparticles
KW - Oximes
KW - Polysaccharides
U2 - 10.1039/b911676a
DO - 10.1039/b911676a
M3 - Journal article
C2 - 19841779
SP - 6367
EP - 6369
JO - Chemical Communications
JF - Chemical Communications
SN - 1359-7345
IS - 42
ER -
ID: 32636580