89821-77-2Relevant articles and documents
Synthesis of the hyper-branched core tetrasaccharide motif of chloroviruses
Mishra, Bijoyananda,Manmode, Sujit,Walke, Gulab,Chakraborty, Saptashwa,Neralkar, Mahesh,Hotha, Srinivas
, p. 1315 - 1328 (2021/02/26)
Chemical synthesis of complex oligosaccharides, especially those possessing hyper-branched structures with one or multiple 1,2-cisglycosidic bonds, is a challenging task. Complementary reactivity of glycosyl donors and acceptors and proper tuning of the s
Glycoconjugates and use thereof as vaccine against Shigella flexneri serotype 3a and X
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Page/Page column 87-89, (2014/09/03)
The present invention relates to compounds derived from sugars which reproduce the epitopes of Shigella flexneri serotypes 3a and X and to the use thereof for the preparation of vaccine compositions. More specifically, the subject matter of the present in
Studies on carbohydrates XVIII. Synthesis of tetrasaccharide corresponding to biological repeat units of Serratia marcescens O18 polysaccharide
Zhang,Mao,Chen,Cai
, p. 2283 - 2290 (2007/10/02)
The synthesis of a blocked tetrasaccharide portion of the biological repeat unit, [→2)L-Rhapα(1→2)L-Rhapα(1→2)L-Rhapα(1→6)D-GlcNAcpα(1→], of the Serratia marcescens O18 polysaccharide was described. The key intermediate compounds was 3,4-blocked -L-rhamno