The chemistry of L-ascorbic and D-isoascorbic acids. 2. R and S glyceraldehydes from a common intermediate
β Scribed by Mikkilineni, Amarendra B.; Kumar, Praveen; Abushanab, Elie
- Book ID
- 126942036
- Publisher
- American Chemical Society
- Year
- 1988
- Tongue
- English
- Weight
- 701 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Ascorbic and D-isoascorbic acids were employed in syntheses of 9-(2 0 ,3 0 ,4 0 -trihydroxybutyl)adenines protected at 3 0 and 4 0 oxygens (all four enantiomers) and at 2 0 oxygen (2 0 S,3 0 R and 2 0 S,3 0 S enantiomers).
Taking advantage of the high functionality of an enantiopure protected syn-2R-amino-l,3,4-triol derivative, easily available on a multigram scale from Disoascorbic acid, several biologically active compounds have been synthesized such as the (2S,3R)-3-amino-2-hydroxydecanoic acid (AHDA), the N-termi