The use of versatile intermediates is very important for various oligosaccharide syntheses. Choices of the suitable protective groups are important for regio- and stereo-selective oligosaccharides syntheses. Synthetic strategy often determines whether the synthesis is successful or not. Protective groups must hold up against a variety of reaction conditions to construct an organic molecule but each group must be de-protected selectively for the following reaction. Thus, selective introduction and removal of protective groups are important in organic chemistry.
The page below shows chemical synthetic reagents and enzymes.
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Glycoscience
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Cyclodextrins [Functional Oligosaccharides]
Glycolipids [Functional Oligosaccharides]
Glycoproteins, Glycopeptides [Functional Oligosaccharides]
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Milk Oligosaccharides [Functional Oligosaccharides]
Natural Glycosides [Functional Oligosaccharides]
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Phosphated Sugars [Functional Oligosaccharides]
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Glycosyl Azides, Aminoethyl Glycosides, Aminopropyl Glycosides [Glyco Building Blocks]
Glycosyl Donors [Glyco Building Blocks]
MP Glycosides [Glyco Building Blocks]
Protected Sugars [Oligosaccharides by Component Sugar]
Sugar Building Blocks by Target Oligosaccharides
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Alloses [Glycoscience]
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