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.
โฆ LIBER โฆ
Determination of the Absolute Stereochemistry of Cyclosmenospongine
โ Scribed by Utkina, Natalia K.; Denisenko, Vladimir A.; Scholokova, Olga V.; Makarchenko, Aleksandra E.
- Book ID
- 126957106
- Publisher
- American Chemical Society
- Year
- 2003
- Tongue
- English
- Weight
- 55 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0163-3864
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Determination of the absolute stereochem
โ
Esther Vaz; Miryam Fernandez-Suarez; Luis Muรฑoz
๐
Article
๐
2003
๐
Elsevier Science
๐
English
โ 178 KB
Determination of the Absolute Stereochem
โ
Esther Vaz; Miryam Fernandez-Suarez; Luis Munoz
๐
Article
๐
2003
๐
John Wiley and Sons
โ 57 KB
๐ 2 views
## Abstract For Abstract see ChemInform Abstract in Full Text.
Determination of absolute stereochemistr
โ
Chul Shim Sang; Yeong Koh Hun; Chang Suk-ku
๐
Article
๐
1985
๐
Elsevier Science
๐
French
โ 123 KB
## Absolute stereochemistry of panaxynol was determined by exciton chirality method.
Absolute Stereochemistry Determination o
โ
Geonseek Ryu; Byoung Wook Choi; Bong Ho Lee
๐
Article
๐
2003
๐
John Wiley and Sons
โ 70 KB
๐ 2 views
Determination of the Absolute Stereochem
โ
Tse, Bruno; Blazey, Charles M.; Tu, Ben; Balkovec, James
๐
Article
๐
1997
๐
American Chemical Society
๐
English
โ 186 KB
First enantioselective synthesis of (+)-
โ
Naoki Toyooka; Hideo Nemoto
๐
Article
๐
2003
๐
Elsevier Science
๐
French
โ 205 KB
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.