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Targeting Cysteine Thiols for in Vitro Site-specific Glycosylation of Recombinant Proteins
Published on: October 4, 2017
Synthetic study of cytosaminomycins using the intramolecular glycosylation as a key step
1Faculty of Education, Yokohama National University, Tokiwadai 79-2, Hodogaya-ku, Yokohama 240-8501, Japan.
Nucleic Acids Research. Supplement (2001)
|September 27, 2003
Abstract:
2',6'-Dideoxy-beta-D-hexopyranosyl pyrimidine nucleoside, which is a component of anticoccidal antibiotics--cytosaminomycins, was synthesized in a stereoselective manner via the intramolecular pyrimidine delivery method. Further glycosylaion of the 4'-position with a glycosyl fluoride gave the disaccharide nucleoside skeleton of the cytosaminomycins.
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