5531-09-9Relevant articles and documents
Synthesis of heparin saccharides. V. Anomeric O benzyl derivatives of L idopyranosyluronic acid
Kiss,Wyss
, p. 1399 - 1402 (1976)
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ACIDIC DYSTROGLYCAN OLIGOSACCHARIDE COMPOUND AND METHOD FOR MAKING SAME
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Paragraph 0074; 00113; 00130, (2019/07/20)
A synthetic dystroglycan oligosaccharide comprising Formula (I) wherein a repeating disaccharide motif consists of Glucuronic Acid (ClcA) and Xylose (Xyl) having a defined glycosyl connection GlcA-β-(1→3)-Xyl-α-(1→3)-GlcA; wherein either end of the synthetic dystroglycan oligosaccharide is conjugatable with chemical or biological vehicle or support; wherein the non-reducing terminal (II) is conjugatable with any oligosaccharides or groups that can modify a hydroxyl functionality; and wherein the reducing terminal is conjugatable with any tags, oligosaccharides or anything that can modify a hydroxyl functionality.
Total synthesis of viscumneoside III of Viscum coloratum
Zou, Lei,Zhang, Zixue,Chen, Xiaowen,Chen, Hua,Zhang, Yi,Li, Jianqi,Liu, Yu
, p. 2376 - 2382 (2018/04/06)
The first total synthesis of viscumneoside III, a promising anti-angina pectoris dihydroflavone O-glycoside isolated from Viscum coloratum was described here. Trichloroaceti-midate was employed as the apiofuranosyl donor to construct the key building block of homoeriodictyol-7-O-β-D-apiosyl-(1 → 2)-β-D-glycoside (1). The longest linear sequence (from 2 to 1) in the synthetic route required thirteen steps and afforded the final product 1 with an overall yield of 6.3%.