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
No coin nor oath required. For personal study only.
✦ 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.
📜 SIMILAR VOLUMES
## 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