作者:Hiroki Soeda、Ryo Towada、Yusuke Ogura、Tomoyo Mohri、Georg Pohnert、Shigefumi Kuwahara
DOI:10.1016/j.tet.2019.02.012
日期:2019.3
The proposed structure for a moss-produced acetylenic oxylipin (10-keto-type structure) was synthesized from a known glycidol derivative by an 11-step sequence involving epoxide ring opening with a terminal acetylene and enzymatic hydrolysis of a methyl ester intermediate. The NMR spectra of the proposed structure was, however, different from those of the natural oxylipin, which prompted us to synthesize
由已知的缩水甘油衍生物通过11步序列合成由苔藓生产的炔基环氧丙烷的拟议结构(10-酮型结构),该步骤涉及用末端乙炔进行环氧基开环和甲酯中间体的酶促水解。但是,所提出结构的NMR谱图不同于天然脂蛋白的NMR谱图,这促使我们合成其9-表位异构体和两个非对映体12-酮型位置异构体。三种异构体的NMR谱与天然脂类的NMR谱的比较表明,天然脂族实际上是两种非对映异构体位置异构体的混合物。