Journal
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
Volume 6, Issue -, Pages -Publisher
BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.6.18
Keywords
block synthesis; human milk oligosaccharides; sialyllacto-N-neotetraose epimer; sialyllacto-N-tetraose; trisaccharide thioglycoside donors
Categories
Funding
- Deutsche Forschungsgemeinschaft [470, A5]
- Fonds der Chemischen Industrie
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alpha,2-3- and alpha,2-6-sialylated lactosaminide precursor structures obtained by various enzymatic procedures could be used for glycosylations employing triflic acid/N-iodosuccinimide. Easily accessible selectively protected lactoside derivatives served as acceptor disaccharides to give the corresponding human milk pentasaccharides in good yields. These were characterized by spectroscopic means in the form of their peracetylated derivatives.
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