A novel approach to synthesis of tricyclic diterpenoid
Author/Authors :
Peng، نويسنده , , Xuanjia and She، نويسنده , , Xuegong and Su، نويسنده , , Ying and Wu، نويسنده , , Tongxin and Pan، نويسنده , , Xinfu، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2004
Pages :
3
From page :
3283
To page :
3285
Abstract :
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.
