posted on 2018-05-14, 00:00authored byShuang Yang, Qi Liu, Guangyan Zhang, Xiaoxi Zhang, Zhehui Zhao, Pingsheng Lei
An
approach was developed to synthesize chondroitin sulfate-E (CS-E)
oligosaccharides by adopting a postglycosylation-transformation strategy:
different from all of the traditional approaches, the characteristic
groups of CS-E were introduced following the assembly of the oligosaccharides.
The adjusted strategy rendered an easy chain elongation strategy.
All of the elongation steps generated high yields with excellent glycosylation
outcomes. An orthogonally protected disaccharide was used as the building
block to provide flexibility for the group transformation and derivatization
at the N-2 position of the GalNAc residue and the O-1,5 positions of the GlcA residue, thereby providing ready
access for the further examination of the structure–activity
relationship (SAR) of CS-E molecules.