Deprotected C-glycopyranosyl-ketones have been conjugated by a chemoselective approach to a peptide or an amino acid bearing an aminooxy group on the N-terminus or on the side-chain, respectively. The coupling reaction, performed in aqueous media, does not require protecting groups on the peptide or saccharide moieties, nor auxiliary coupling reagents.

Peri, F., Cipolla, L., LA FERLA, B., Dumy, P., Nicotra, F. (1999). A highly convergent approach to O- and N-linked glycopeptide analogues. GLYCOCONJUGATE JOURNAL, 16, 399-404.

A highly convergent approach to O- and N-linked glycopeptide analogues

PERI, FRANCESCO;CIPOLLA, LAURA FRANCESCA;LA FERLA, BARBARA;NICOTRA, FRANCESCO
1999

Abstract

Deprotected C-glycopyranosyl-ketones have been conjugated by a chemoselective approach to a peptide or an amino acid bearing an aminooxy group on the N-terminus or on the side-chain, respectively. The coupling reaction, performed in aqueous media, does not require protecting groups on the peptide or saccharide moieties, nor auxiliary coupling reagents.
Articolo in rivista - Articolo scientifico
GLYCOPEPTIDES, PEPTIDOMIMETICS
English
399
404
6
Peri, F., Cipolla, L., LA FERLA, B., Dumy, P., Nicotra, F. (1999). A highly convergent approach to O- and N-linked glycopeptide analogues. GLYCOCONJUGATE JOURNAL, 16, 399-404.
Peri, F; Cipolla, L; LA FERLA, B; Dumy, P; Nicotra, F
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/16935
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