151072-07-0Relevant articles and documents
Protecting groups for carbohydrate synthesis
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Page/Page column 20-21, (2010/02/14)
The invention provides collections of orthogonally-protected monosaccharides as universal building blocks for the synthesis of glycoconjugates of non-carbohydrate molecules, neo-glycoconjugates and oligosaccharides. This orthogonal protection strategy all
Synthesis of a tetrasaccharide donor corresponding to the O-specific polysaccharide of Shigella dysenteriae type 1
Pozsgay,Glaudemans,Robbins,Schneerson
, p. 259 - 273 (2007/10/02)
O-(2,4-Di-O-benzoyl-3-O-chloroacetyl-α-L-rhamnopyranosyl)-(1 → 2)-O-(3,4,6-tri-O-benzoyl-α-D-galactopyranosyl)-(1 → 3)-O-(2-acetamido-4,6-di-O-acetyl-2-deoxy-α-D-glucopyranosyl)-(1 → 3)-2,4-di-O-benzoyl-α-L-rhamnopyranosyl trichloroacetimidate (1) was syn