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Updated: Sep 20, 2026

Chemo-enzymatic Synthesis of N-glycans for Array Development and HIV Antibody Profiling
Published on: February 5, 2018
Synthesis of an unnatural N-glycan-linked dolichyl pyrophosphate precursor
Yuko Nakahara1, Tomoharu Nonaka, Hironobu Hojo
1Institute of Glycotechnology, Department of Applied Biochemistry, Tokai University, Kitakaname 1117, Hiratsuka, Kanagawa 259-1292, Japan.
Abstract:
An unnatural alpha-D-mannopyranose-linked chitobiosyl dolichyl pyrophosphate, a stereoisomer of the N-glycan biosynthesis intermediate, was synthesized. The protected trisaccharide, alpha-D-Man-(1-->4)-beta-D-GlcNAc-(1-->4)-D-GlcNAc, carrying a 4-methylbenzoyl group was prepared for the convenience of a TLC analysis. 1-O-Phosphorylation, condensation with dolichyl phosphate, and subsequent deprotection afforded the title compound.
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