The title compound, C 18 H 22 O 7 S, is the product of the per-Oacetylation and thioglycosylation of the hexose l-(+)rhamnopyranose. The structure has a chair conformation and the thiophenyl group on the anomeric carbon (C-1) is in an axial position.
✦ LIBER ✦
A simple method for the synthesis of ethyl 2,3,4-tri-O-acetyl-1-thio-β-l-rhamnopyranoside
✍ Scribed by Tsuyoshi Fujiwara; Kiyoshi Arai
- Book ID
- 108308822
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- English
- Weight
- 195 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0008-6215
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