1H NMR, electronic-absorption and resonance-Raman spectra of isomeric okenone as compared with those of isomeric β-carotene, canthaxanthin, β-apo-8′-carotenal and spheroidene-Reference-Cited by-同舟云学术

1H NMR, electronic-absorption and resonance-Raman spectra of isomeric okenone as compared with those of isomeric β-carotene, canthaxanthin, β-apo-8′-carotenal and spheroidene

Published:1998-05 Issue:5 Volume:54 Page:727-743
ISSN:1386-1425
Container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
language:en
Short-container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy

Author:

Fujii Ritsuko,Chen Chun-Hai,Mizoguchi Tadashi,Koyama Yasushi

Publisher

Elsevier BV

Subject

Spectroscopy,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry

Reference20 articles.

1. 1H NMR spectra of the all-trans, 7-cis, 9-cis, 13-cis and 15-cis isomers of β-carotene: elongation of the double bond and shortening of the single bond toward the center of the conjugated chain as revealed by vicinal coupling constants

2. Y. Hu, H. Hashimoto, G. Moine, U. Hengartner, Y. Koyama, J. Chem. Soc. Perkin II (1997) 2699.

3. Raman and infrared spectra of the all-trans, 7-cis, 9-cis, 13-cis and 15-cis isomers of β-carotene: Key bands distinguishing stretched or terminal-bent configurations form central-bent configurations

4. Isolation of cis-trans isomers of canthaxanthin by high-performance liquid chromatography using a calcium hydroxide column and identification of their configurations by 1H NMR spectroscopy

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