Department of Chemistry, York University, M3J IP3, Downsview, Ontario, Canada.
J Chem Ecol. 1984 May;10(5):795-807. doi: 10.1007/BF00988544.
The title compounds were prepared by six different routes, and recommendations are given for the more convenient procedures in laboratory-scale syntheses. Modifications in the literature preparations of the 9E,11E and 9E,11Z isomers are described. Baseline separation of a prepared mixture of all four isomers of the (9Z, 11Z), (9E, 11E), (9E, 11Z), and (9Z, 11E)-9,11-hexadecadienals was achieved using GC methods with standard capillary columns. [(13)C]NMR spectroscopy of the alkene carbon atoms clearly differentiates between theZ,Z, E,E and eitherE,Z orZ,E isomers of the precursor dienols and thus of the dienals.
标题化合物通过六种不同的路线制备,并为实验室规模合成中更方便的程序提供了建议。描述了文献中制备 9E,11E 和 9E,11Z 异构体的修改。使用 GC 方法和标准毛细管柱对(9Z,11Z)、(9E,11E)、(9E,11Z)和(9Z,11E)-9,11-十六碳二烯醛的所有四种异构体的混合物进行了基线分离。烯碳原子的[(13)C]NMR 光谱清楚地区分了前体二烯醇的 Z,Z,E,E 和 E,Z 或 Z,E 异构体,因此也区分了二烯醛。