Syntheses of 2',3'-Dideoxy-D-C-nucleosides from γ-Lactone. -A versatile method for the synthesis of 2',3'-dideoxy-D-C-nucleosides such as (X)/(XI) and (XVII)/(XVIII) starting from γ-lactone (I) is presented. None of the target compounds shows significant activities against HBV and HIV as well as si
✦ LIBER ✦
γ-Spiroketal γ-Lactones from 2-(γ-Hydroxyalkyl)furans: Syntheses of epi -Pyrenolides D and Crassalactone D
✍ Scribed by Pavlakos, Elias; Georgiou, Thomas; Tofi, Maria; Montagnon, Tamsyn; Vassilikogiannakis, Georgios
- Book ID
- 117990008
- Publisher
- American Chemical Society
- Year
- 2009
- Tongue
- English
- Weight
- 266 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1523-7060
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
ChemInform Abstract: Syntheses of 2′,3′-
✍
Y. XIANG; J. DU; C. K. CHU
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 35 KB
👁 1 views
ChemInform Abstract: Direct Synthesis of
✍
R. D. RIEKE; M. S. SELL; H. XIONG
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 37 KB
ChemInform Abstract: Novel Syntheses of
✍
A. R. KATRITZKY; D. FENG; H. LANG
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 33 KB
👁 1 views
Stereochemical features of the [1,2]-Wit
✍
Katsuhiko Tomooka; Makoto Kikuchi; Kazunobu Igawa; Ping-Huai Keong; Takeshi Naka
📂
Article
📅
1999
🏛
Elsevier Science
🌐
French
⚖ 247 KB
The Winig rearrangement of D-galactono-y-lactone derived [~O-glycoside is shown to al't~rd [5-C-glycoside (retention product), a potentially useful intermediate tbr zaragozic acid synthesis. By contrast, the rearrangement of the D-xylonolactone-derived counterpart was found to violate the retention
ChemInform Abstract: Stereochemical Feat
✍
Katsuhiko Tomooka; Makoto Kikuchi; Kazunobu Igawa; Ping-Huai Keong; Takeshi Naka
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 36 KB
👁 2 views