## Abstract For Abstract see ChemInform Abstract in Full Text.
Determination of the absolute stereochemistry of Etzionin
✍ Scribed by Esther Vaz; Miryam Fernandez-Suarez; Luis Muñoz
- Book ID
- 104359913
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 178 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0957-4166
No coin nor oath required. For personal study only.
✦ Synopsis
The absolute configuration of Etzionin, a marine peptide-like compound isolated in 1989 from a red tunicate collected from the Red Sea has been determined by a combination of synthetic and spectroscopic procedures. Finally, its absolute stereochemistry has been established as 3S,3%R.
📜 SIMILAR VOLUMES
## Absolute stereochemistry of panaxynol was determined by exciton chirality method.
First enantioselective synthesis of quinolizidine 207I has been achieved and the absolute stereochemistry of natural quinolizidine 207I was determined to be 1S,4S,10S by the present chiral synthesis using GC analysis with b-dextrin chiral column on co-injection with racemate.