Author/Authors :
Tian، نويسنده , , Hua and Jiao، نويسنده , , Xiaozhen and Xie، نويسنده , , Ping and Liang، نويسنده , , Xiaotian، نويسنده ,
Abstract :
The first total synthesis of beauveriolide I (1a), a selective ACAT inhibitor, is described. The key steps in this synthesis involved a diastereoselective aldol condensation sequence and a macrocyclization.
