A Solution to Chemical Pseudaminylation via a Bimodal Glycosyl Donor for Highly Stereocontrolled α- and β-Glycosylation
Author:
Affiliation:
1. Department of Chemistry, State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Hong Kong, P. R. China
2. School of Chemistry, The University of Sydney, Sydney, Australia
Funder
Research Grants Council, University Grants Committee
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b00990
Reference40 articles.
1. Sialic acids of a new type from the lipopolysaccharides of Pseudomonas aeruginosa and Shigella boydii
2. The occurrence and biological significance of the α-keto-sugars pseudaminic acid and legionaminic acid within pathogenic bacteria
3. Structure of a new pseudaminic acid-containing capsular polysaccharide of Acinetobacter baumannii LUH5550 having the KL42 capsule biosynthesis locus
4. Structure of the capsular polysaccharide of Acinetobacter baumannii ACICU containing di-N-acetylpseudaminic acid
5. Chemical structure of the carbohydrate backbone of the lipopolysaccharide from Piscirickettsia salmonis
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