Highly Efficient Regio- and Stereoselective Synthesis of β-(1→6)-Branched β-(1→3)-Linked Glucohexaose and Its Analogue
✍ Scribed by Yue-Tao Yi; Qian-Fei Zhao; Feng-Zhen Qian; Jun Ning
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 87 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0256-7660
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📜 SIMILAR VOLUMES
The branched, sulfur-linked tetrasaccharide S-(beta-D-glucopyranosyl)-(1-->3)-S-[(6-S-beta-D-glucopyranosyl)-3,6-dit hio- beta-D-glucopyranosyl]-(1-->3)-S-3-thio-D-glucopyranose (9) has been conveniently prepared by SN2 displacement of the triflate group in 1,2:5,6-di-O-isopropylidene-3-O-trifluorom
## Abstract Lauryl glycoside of β‐__D__‐Gic__p__‐(1 → 3)‐[β‐__D__‐Glc__p__‐(1 → 6)‐] __a__‐__D__‐Glc__p__‐(1 → 3)‐β‐__D__‐Glc__p__‐(1 → 3)‐[β‐__D__‐Glc__p__‐(1 → 6)‐] __a__‐__D__‐Glc__p__‐(1 → 3)‐β‐__D__‐Glc__p__‐(1 → 3)‐[β‐__D__‐Glc__p__‐(1 → 6)‐]β‐__D__‐Glc__p__ was synthesized through 3 + 3 + 3
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