Abstract
An efficient synthesis of buffalo milk pentasaccharide derivative via a 3+2 strategy is described. The use of a trisaccharide isopropyl thioglycoside as a latent glycosyl donor and the application of two well-defined regioselective glycosylations significantly simplified the target preparation.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Buffaloes
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Carbohydrate Conformation
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Carbohydrate Sequence
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Milk / chemistry*
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Models, Molecular
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Molecular Sequence Data
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Oligosaccharides / chemical synthesis*
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Oligosaccharides / chemistry
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Oligosaccharides / isolation & purification