摘要
An efficient and simple procedure for the synthesis of novel isatin derivatives is described. Michael addition of aniline Schiff bases of isatin or p-toluidine Schiff bases of isatin to fumaric esters affords the Michael adduct com- pounds in good to high yields in the presence of K2CO3 and tetrabutylammonium bromide （TBAB） under sol- vent-free conditions. Repeating of this reaction about spiro[l,3-dioxolane-2,3＇-indol]-2＇（l＇H）-one, as a Michael do- nor, in the presence of 1,4-diazabicyclo[2.2.2]octane （DABCO） gives Michael adducts in remarkable yields under the same conditions.
An efficient and simple procedure for the synthesis of novel isatin derivatives is described. Michael addition of aniline Schiff bases of isatin or p-toluidine Schiff bases of isatin to fumaric esters affords the Michael adduct com- pounds in good to high yields in the presence of K2CO3 and tetrabutylammonium bromide （TBAB） under sol- vent-free conditions. Repeating of this reaction about spiro[l,3-dioxolane-2,3＇-indol]-2＇（l＇H）-one, as a Michael do- nor, in the presence of 1,4-diazabicyclo[2.2.2]octane （DABCO） gives Michael adducts in remarkable yields under the same conditions.
