Takahashi Kazunori, Akao Ryuichi, Honda Toshio
Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41, Shinagawa-ku, Tokyo 142-8501, Japan.
J Org Chem. 2009 May 1;74(9):3424-9. doi: 10.1021/jo900369t.
Diastereoselective total synthesis of trifarienols A and B, trifarane-type sesquiterpenes isolated from the Malaysian Cheilolejeunea trifaria, was achieved via an intramolecular Hosomi-Sakurai reaction of the aldehyde to construct a substituted bicyclo[3.3.1]nonane skeleton having the exo-methylene moiety of the target compounds in one step.
从马来西亚的三瓣唇鳞苔中分离得到的三瓣苔醇A和B(三瓣烷型倍半萜)的非对映选择性全合成,是通过醛的分子内保土谷-樱井反应一步构建具有目标化合物外亚甲基部分的取代双环[3.3.1]壬烷骨架来实现的。