作者:Xuanjia Peng、Xuegong She、Ying Su、Tongxin Wu、Xinfu Pan
DOI:10.1016/j.tetlet.2004.02.136
日期:2004.4
A novel approach has been found and the first total synthesis of (±)-Salvirecognine was accomplished by using it. In which intramolecular cyclization and Friedel–Crafts alkylation took place simultaneously to afford key intermediates for synthesis of aromatic tricyclic diterpenoids.
已经发现了一种新颖的方法,并且通过使用它完成了第一个(±)-Salvirecognine的全合成。其中分子内环化和Friedel-Crafts烷基化同时发生,从而提供了合成芳族三环二萜的关键中间体。