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(E/Z)-Isomerization of 3′-Epilutein
✍ Scribed by Péter Molnár; József Deli; Erzsébet Ősz; Zoltán Matus; Gyula Tóth; Ferenc Zsila
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- German
- Weight
- 250 KB
- Volume
- 87
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
3′‐Epilutein (=(all‐E,3__R__,3′S,6′R)‐4′,5′‐didehydro‐5′,6′‐dihydro‐β,β‐carotene‐3,3′‐diol; 1), isolated from the flowers of Caltha palustris, was submitted to both thermal isomerization and I~2~‐catalyzed photoisomerization. The structures of the main products (9__Z__)‐1, (9′Z)‐1, (13__Z__)‐1, (13′Z)‐1, (15__Z__)‐1, and (9__Z__,9′Z)‐1 were determined based on UV/VIS, CD, ^1^H‐NMR, and MS data.
📜 SIMILAR VOLUMES
1H and 15N NMR chemical shifts of 12 semicyclic amidinium salts are reported. Their E/Z equilibria in solution were analyzed by 1D and 2D 1H and 15N NMR techniques. In the solid state the Z-conÐguration is observed.
## Abstract The temperature and concentration dependence of the ^1^H NMR spectra of four anilinomethylenemalonic acid derivatives were determined in CDCl~3~ and DMSO‐__d__~6~ to assign the __E__–__Z__ isomers and to investigate the formation of intra‐ and intermolecular hydrogen bonds. Chemical shi