Entry into the bi-aryl moiety of the TMC-95 proteasome inhibitors via the Stille protocol
Author/Authors :
Albrecht، نويسنده , , Brian L. and Williams، نويسنده , , Robert M، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2001
Pages :
3
From page :
2755
To page :
2757
Abstract :
The synthesis of the bi-aryl moiety of the TMC-95 natural products has been achieved via a palladium-catalyzed Stille cross-coupling reaction of an aryl stannane tyrosine derivative and 7-iodoisatin.
