Synthesis, Isolation, and Full Spectroscopic Characterization of Eleven (Z)-Isomers of (3R,3′R)-Zeaxanthin
✍ Scribed by Gerhard Englert; Klaus Noack; Emil A. Broger; Ernst Glinz; Max Vecchi; Reinhard Zell
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- German
- Weight
- 818 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
1. Introduction.
-Starting from the optically pure hydroxyketone 1, an efficient synthesis of (3R,3'R)-zeaxanthin (2) was described recently [l]. The final step involves a double Wittig condensation. Developmental efforts to improve the yield of 2 have Scheme. Synthesis of (2.E)-Zeaxanthenals and ( 2 , E ) -2eaxanthins HO 8 ",,, 4 -3 F no e 5 ! j -HO w-c1-1 3 4 (7Z,9E) 5 (7E,9€) 6 (72.92) 7 (7€,92) 2 (all-E) 18 (92.92) 13 (72) 19 (72,92,7'2) 14 (92) 20 (72,112,7'2) 15 (132) 21 (92,132,92) 17 (72,7'2) 23 (72,92,112,7'2,92) 16 (152) 22 (72,92,7'2,92) 9 (all-€) 10 (72) 11 (92) 12 (72,92) I )
📜 SIMILAR VOLUMES
Racemic dg-sulpiride, (R)-(+)-dg-sulpiride and (S)-(-)-dg-sulpiride (with three deuterium atoms in the methoxy function ortho to the benzamide), as well as (R)-(+)-sulpiride and (S)-(-)-sulpiride were synthesized. The structures were characterized by melting points, IR, 1H-NMR, GC-MS and polarimetry