An enantio- and stereocontrolled route to epopromycin B via cinchona alkaloid-catalyzed Baylis–Hillman reaction
Author/Authors :
Iwabuchi، نويسنده , , Yoshiharu and Sugihara، نويسنده , , Tatsuya and Esumi، نويسنده , , Tomoyuki and Hatakeyama، نويسنده , , Susumi، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2001
Pages :
5
From page :
7867
To page :
7871
Abstract :
An enantio- and stereocontrolled route to epopromycin B having the epoxy-β-aminoketone pharmacophore is developed based on the cinchona alkaloid-catalyzed Baylis–Hillman reaction of N-Fmoc-leucinal.
