NMR studies on natural all‐trans‐(9′Z,11′Z)‐(3R,3′S,5′R,6′R)‐pyrrhoxanthin, an acetylenic C37‐skeletal nor‐carotenoid butenolide

Magnetic Resonance in Chemistry

Volumn 31, Issue 10, 1993, Pages 910-915

  Englert, Gerhard ^a   Aakermann, Torunn ^b   Liaaen‐Jensen, Synnøve ^b  

^a F HOFFMANN LA ROCHE LTD   (Switzerland)

^b NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

Author keywords

1H,13C 2D COSY; 1H,1H 2D COSY; Pyrrhoxanthin; ROESY; T ROESY TOCSY

Indexed keywords

EID: 84958369699     PISSN: 07491581     EISSN: 1097458X     Source Type: Journal    
DOI: 10.1002/mrc.1260311007     Document Type: Article

References (23)

1. Synthesis of the 4-alkylidenebutenolide carotenoids, peridinin and pyrrhoxanthin
2. Recent progress in the synthesis of butenolide carotenoids and retinoids
3. NMR of carotenoids - new experimental techniques
4. Configuration of cross-conjugated caroten-20-als: 2D NMR study on four isomers of renierapurpurin-20-al
5. 1D and 2D NMR study of some allenic carotenoids of the fucoxanthin series
6. NMR of carotenoids: novel experimental techniques
7. Structure determination of a tetrasaccharide: transient nuclear Overhauser effects in the rotating frame
8. Algal carotenoids 47-NMR study of all-trans-peridinin, including complete1H and13C NMR assignments
9. Total assignment of the1H and13C spectra of peridinin
10. Algal Carotenoids. 48. Structural Assignments of Geometrical Isomers of Fucoxanthin.