作者:Bernard Riss、Bernard Muckensturm
DOI:10.1016/s0040-4020(01)80090-9
日期:1989.1
Bisabolangelone is a sesquiterpenoid well known for its strong antifeeding properties against phytophagous insects. In this communication, we describe the total synthesis of the target molecule, following a model study, wich shows the possibilities to cyclizise γ-acetylenic alcohols, in view to obtain 2-(2-alkenylidene)-tetrahydrofurans, an essential moiety of bisabolangelone.
Bisabolangelone是一种倍半萜类化合物,以其对食草性昆虫的强抗食性而闻名。在此交流中,我们通过模型研究描述了目标分子的总合成,这表明环化γ-炔醇的可能性,以期获得2-(2-亚链烯基)-四氢呋喃,这是双硼苯醌的基本组成部分。