Preparation and Spectroscopic Characterization of (9Z,9′Z)-Lutein (Neolutein C)
✍ Scribed by Péter Molnár; Erzsébet Ősz; Gyula Tóth; Ferenc Zsila; József Deli
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- German
- Weight
- 89 KB
- Volume
- 89
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The preparation of pure, crystalline (9__Z__,9′Z)‐lutein (neolutein C; 2) by I~2~‐catalyzed photoisomerization of (all‐E)‐lutein (1) is described. The structure of 2 was unambiguously determined by UV/VIS, CD, and NMR spectroscopy, as well as by mass spectrometry, and the complete assignment of the ^13^C‐NMR spectrum of this carotenoid is presented for the first time.
📜 SIMILAR VOLUMES
In order to study the effect of the double bonds geometry of linolenic acid (18:3 n-3) on its biological activities, (gz,12Z, I 5E)-and (9E, I 2Z, 15Z)-octadecatrienoic acids, found in many refined vegetable oils, were made by total synthesis. Synthesis of 18:3 A9c, 12c, 1St involves a Wittig reacti
3Z,6E)-l-Bromododeca-3,6-diene, a common intermediate in the synthesis of labelled 12t linoleic acid and 14t arachidonic acid, was obtained from (E)-3-nonyl-l-ol, in four steps, via conventional functional manipulations. Cross-coupling of this bromododecadiene with the Grignard reagent of l-chloro-5