作者:R. Rossi、A. Carpita
DOI:10.1016/0040-4020(77)80262-7
日期:1977.1
The (S)-enantiomers of (Z)- and (E)-14-methyl-8-hexadecen-1-ol, 1 and 4, respectively, and of (Z)- and (E)-14-methyl-8-hexadecenal, 6 and 7, respectively, which are sex pheromone components of dermestid beetles, have been synthesized in high optical purity starting from optically pure (S)-2-methyl-1-butanol. The preparation of 1 has been carried out using a new general method for reducing stereoselectively
(Z)-和(E)-14-甲基-8-十六烯-1-醇的(S)-对映体分别为1和4,以及(Z)-和(E)-14-甲基-8的(S)-对映体-hexadecenal,6和7,分别,这是皮蠹的性信息素组分,已在由光学纯(启动用高光学纯度被合成小号)-2-甲基-1-丁醇。1的制备已使用一种新的通用方法进行,该方法用于将立体选择性和高产率的ω-炔醇还原为相应的(E)-烯醇。的光学纯的旋光1,4,6和7已经建立。