## Summarv: A novel and efficient synthesis of 2,6-dideoxy-a-glycosides was developed by use of phenyl 2,6-anhydro-1,2-dithio-D-altropyranosides as glycosyl donors in a highly stereocontrolled glycosyla tion . Highly stereocontrolled synthesis of 2,6-dideoxy glycosides is of considerable interest
The use of 2,6-anhydro-2-thio glycopyranosyl fluoride for a highly α-stereoselective glycosylation
✍ Scribed by Kazunobu Toshima; Satsuki Mukaiyama; Takashi Ishiyama; Kuniaki Tatsuta
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 89 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
## Gycosy1ation.r of lhe I-O-aceryl-2,6-anhydro3-thio sugar 3 with alcohols in the presence of several Lewis acids in CH2Cl2 proceeded smoothly to give the corresponding &Cl-glycosides with high srereocontrol in high yields. and the selectivity of the gIycosylaLon was highly independent on Lewis a
1999 carbohydrates carbohydrates U 0500 47 -218 2-Deoxy-2-iodo-α-mannopyranosyl and -talopyranosyl Acetates: Highly Stereoselective Glycosyl Donors for the Synthesis of 2-Deoxyα-glycosides. -Reactions of the title compounds with various glycosyl acceptors in the presence of TmsOTf are found to yiel
## Abstract For Abstract see ChemInform Abstract in Full Text.