Chemical preparation of sialyl Lewis x using an enzymatically synthesized sialoside building block
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Hierarchical and Programmable One-Pot Oligosaccharide Synthesis
Published on: September 6, 2019
Hongzhi Cao1, Shengshu Huang, Jiansong Cheng
1Department of Chemistry, University of California, One Shields Avenue, Davis, CA 95616, USA.
Abstract:
The sialyl Lewis x tetrasaccharide with a propylamine aglycon was assembled by chemoselective glycosylation from a p-tolyl thioglycosyl donor obtained from an enzymatically synthesized sialodisaccharide. Combining the advantages of highly efficient enzymatic synthesis of sialoside building blocks, and diverse chemical glycosylation, this chemoenzymatic approach is practical for obtaining complex sialosides and their analogues.
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