138730-66-2Relevant academic research and scientific papers
Synthesis of 2-aminoethyl glycosides of chitooligosaccharides
Yudina,Tsvetkov, Yu. E.,Nifantiev
, p. 2932 - 2941 (2016/09/28)
2-Aminoethyl glycosides of chitotriose, chitopentaose, and chitoheptaose were synthesized. The successive extension of the oligosaccharide chain by two monosaccharide residues was carried out using a monosaccharide acceptor and a disaccharide donor, in which amino groups were protected by phthaloyl groups, benzyl moieties were used as a permanent protection for the hydroxy groups at C(3) and C(6), and acetyl or chloroacetyl groups were employed as a temporary protection for the hydroxy group at C(4).
Synthesis of a core trisaccharide as a versatile building block for N-glycans and glycoconjugates
Unverzagt, Carlo
, p. 1369 - 1376 (2007/10/03)
N-Linked oligosaccharides from glycoproteins (N-glycans) can be conveniently assembled with a building block approach. A protected form of the core trisaccharide (β-mannosyl chitobiose) was identified as a key building block. The chitobiose part of the co
Synthesis of fully and partially benzylated glycosyl azides via thioalkyl glycosides as precursors for the preparation of N-glycopeptides
Kerekgyarto, Janos,Agoston, Karoly,Batta, Gyula,Kamerling, Johannis P.,Vliegenthart, Johannes F. G.
, p. 7189 - 7192 (2007/10/03)
Fully O-benzylated mono-, di- and trisaccharide glycosyl azides representing the reducing terminal of the core structure of N-glycans were synthesized. Totally and partially benzylated thioalkyl glucosamine glycosides were converted into the corresponding
