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Updated: Apr 6, 2026

Metabolic Glycoengineering of Sialic Acid Using N-acyl-modified Mannosamines
Published on: November 25, 2017
β-Mannosylation with 4,6-benzylidene protected mannosyl donors without preactivation
Mads Heuckendorff1, Pernille Sørensen Bols, Collin Bartholomew Barry
1Department of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen Ø, Denmark. cmp@chem.ku.dk bols@chem.ku.dk.
Abstract:
Mannosylations with benzylidene protected mannosyl donors were found to be β-selective even when no preactivation was performed. It was also found that the kinetic β-product in some cases anomerizes fast to the thermodynamically favored α-anomer under typical reaction conditions.
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