RUS  ENG
Full version
JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2019 Volume 29, Issue 6, Pages 680–682 (Mi mendc1629)

Communications

Synthesis of N-acetyllactosamine based branched hexasaccharide

I. M. Ryzhov, M. S. Savchenko, G. V. Pazynina, S. V. Tsygankova, I. S. Popova, T. V. Tyrtysh, N. V. Bovin

M.M. Shemyakin–Yu.A. Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: The protected spacer-armed branched tri-N-acetyllactosamine has been synthesized as a building block for the synthesis of biantennary ABH blood group antigens. The key synthetic step is the simultaneous glycosylation of the 3′- and 6′-OH groups of an N-acetyllactosamine glycosyl acceptor by N-Troc-lactosamine trichloroacetimidate.

Language: English

DOI: 10.1016/j.mencom.2019.11.026



© Steklov Math. Inst. of RAS, 2025