## Abstract The allenic C~37~ skeletal carotenoid all‐__trans__‐(3__S__, 5__R__, 6__R__, 3′__S__, 5′__R__, 6′__S__)‐peridinin, isolated from __Amphidinium carterae__ by an improved isolation procedure, was subjected to a detailed ^1^H and ^13^C NMR spectroscopic analysis. Complete assignments of th
NMR assignments of selected bacterial carotenoids
✍ Scribed by Bjart Frode Lutnaes; Jostein Krane; Synnøve Liaaen-Jensen
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 81 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1102
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✦ Synopsis
Abstract
Complete ^1^H and ^13^C NMR assignments for selected carotenoids from purple and green phototropic bacteria are reported for the first time. Assignments are made for the all‐E isomers of OH‐rhodopin (1, 1,2,1′,2′‐tetrahydro‐ψ,ψ‐carotene‐1,1′‐diol), rhodovibrin (2, 1′‐methoxy‐3′,4′‐didehydro‐1,2,1′,2′‐tetrahydro‐ψ,ψ‐carotene‐1‐ol), anhydrorhodovibrin (3, 1‐methoxy‐3,4‐didehydro‐1,2‐dihydro‐ψ,ψ‐carotene), 2‐ketorhodovibrin (4, 1′‐hydroxy‐1‐methoxy‐3,4,3′,4′‐tetradehydro‐1,2, 1′,2′‐tetrahydro‐ψ,ψ‐carotene‐2‐one) and chlorobactene (5, ϕ,ψ‐carotene). Copyright © 2002 John Wiley & Sons, Ltd.
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