The NMR spectra of olefinic protons in the four representative conjugated fatty acid methyl esters, methyl cis ‐9, trans ‐11‐octadecadienoate, methyl trans ‐9, trans ‐11‐octadecadienoate, methyl α eleostearate, and methyl β eleostearate, were studied. The chemical shift of each olefinic proton in these compounds was determined by considering their intramolecular environment. Coupling constants were also obtained as the results of spectral analysis.
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Suzuki et al. (1970) studied this question.
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