Chemical speculation on the biosynthesis of hyperelodione D leads to its structural reassignment via a concise total synthesis. The key step is a bioinspired, Diels–Alder cascade reaction between E,E-α-farnesene and a naturally occurring quinone that generates three rings and six stereocentres.
对 Hyperelodione D
生物合成的
化学推测通过简明的全合成导致其结构重新分配。关键步骤是E 、 E - α-法呢烯和天然醌之间的仿生狄尔斯-阿尔德级联反应,产生三个环和六个立构中心。