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Direct synthesis of β-d-Xyl-(1→2)-β-d-Man-(1→4)-α-d-Glc-OME: a trisaccharide component of the Hyriopsis schlegelii glycosphingolipid

✍ Scribed by David Crich; Zongmin Dai


Book ID
104258906
Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
179 KB
Volume
39
Category
Article
ISSN
0040-4039

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✦ Synopsis


Almtraet. A synthesis of the target trisaccharide is described in which the key l~,-mannosylation is achieved in high yield and selectivity through reaction of the sulfoxide 7 with acceptor 8, meAiated with triflic anhydride.

The xylosylation was best coudueted using trihenzoyl xylopyranosyl bromide and silver triflate.


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Synthesis of Protected Hexp-(1 → 4)-β-D-
✍ van Dorst, Johannes A. L. M. ;Voskamp, Anton F. ;Kamerling, Johannis P. ;Vliegen 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 866 KB

## Abstract Three trisaccharide derivatives of the type β‐D‐Hex__p__‐(1 → 4)‐β‐D‐Glc__p__NAc(1 → 2)‐α‐D‐Man__p__‐(1 → O)(CH~2~)~7~CH~3~ have been synthesized, with Hex being either glucose (15), 4‐deoxy‐4‐fluorogalactose (20), or 4‐deoxygalactose (27). These trisaccharides have been designed for th