AbstractA metal‐free intramolecular annulation of 2‐aryloxybenzaldehydes to xanthones is disclosed, which proceeds through the direct oxidative coupling of an aldehyde CH bond and aromatic CH bonds using tetrabutylammonium bromide (TBAB) as a promoter in aqueous medium. This strategy works smoothly in the presence of both electron‐donating and electron‐withdrawing groups, and displays good tolerance towards catalytically reactive substituents, thus promising further functionalizations of xanthone products.magnified image
AbstractA metal‐free intramolecular annulation of 2‐aryloxybenzaldehydes to xanthones is disclosed, which proceeds through the direct oxidative coupling of an aldehyde CH bond and aromatic CH bonds using tetrabutylammonium bromide (TBAB) as a promoter in aqueous medium. This strategy works smoothly in the presence of both electron‐donating and electron‐withdrawing groups, and displays good tolerance towards catalytically reactive substituents, thus promising further functionalizations of xanthone products.magnified image
[EN] SPIROINDOLINONE DERIVATIVES<br/>[FR] DÉRIVÉS DE SPIROINDOLINONE
申请人:HOFFMANN LA ROCHE
公开号:WO2009077357A1
公开(公告)日:2009-06-25
There are provided compounds of the formula (I), and pharmaceutically acceptable salts and esters thereof, wherein W, V, X, Y, A, R and R' are as described herein, processes for making said compounds and methods for using them, in particular as anticancer agents.