Glass R L, Krick T P, Sand D M, Rahn C H, Schlenk H
Lipids. 1975 Nov;10(11):695-702. doi: 10.1007/BF02532763.
Fatty acids, recently reported as constituents of certain fish lipids, were identified to be derivatives of furan (furanoid fish fatty acids). 12,15-Epoxy-13,14-dimethyleicosa-12,14-dienoic acid is predominant among the furan acids and is associated with bis-homologs in regard to chain length. Monomethyl acids, such as 12,15-epoxy-13-methyleicosa-12,14-dienoic, are present in appreciable amounts. The structures were concluded from oxidative degradations, from mass spectrometry of methyl esters of the novel acids and fatty acids derived from them by opening the ring, and from nuclear magnetic resonance, infrared, and Raman spectra. The results from chemical procedures and from spectrometric methods were in agreement with those obtained with authentic methyl 9,12-epoxyoctadeca-9,11-dienoate. The number of substituents at the furan ring greatly influences hydrogenation, hydrogenolysis, and hydrolysis reactions of the ring.
脂肪酸,最近被报道为某些鱼类脂质的成分,被鉴定为呋喃的衍生物(呋喃类鱼脂肪酸)。12,15-环氧-13,14-二甲基二十碳-12,14-二烯酸是呋喃酸中占主导地位的,并且在链长方面与双同系物相关。单甲基酸,如12,15-环氧-13-甲基二十碳-12,14-二烯酸,大量存在。这些结构是通过氧化降解、新型酸及其开环衍生的脂肪酸甲酯的质谱分析以及核磁共振、红外和拉曼光谱得出的。化学程序和光谱方法的结果与用 authentic methyl 9,12-epoxyoctadeca-9,11-dienoate得到的结果一致。呋喃环上取代基的数量极大地影响环的氢化、氢解和水解反应。