Synthesis and application of modified silica sulfuric acid as a solid acid heterogeneous catalyst in Michael addition reactions
作者:Mohammad Ali Zolfigol、Hojat Veisi、Farajollah Mohanazadeh、Alireza Sedrpoushan
DOI:10.1002/jhet.659
日期:2011.7
Modified silicasulfuricacid (MSSA) as a new type of silicasulfuricacid was prepared and effectively used in the conjugate addition of indole, pyrrole, and thiols with Michael acceptors under mild conditions at room temperature. Also, MSSA was used as a catalyst for the synthesis of 1,1,3‐tri‐indolyl compounds in good to excellent yield at room temperature. J. Heterocyclic Chem., (2011).
We evaluated the influence of solvent on the alumina‐promoted C3‐alkylation of indoles with α,β‐unsaturatedketones. We found that lipophilic solvents were generally superior to hydrophilic ones with hexanes offering the 3‐alkyl indole products in high yields. Thus, we demonstrate an inexpensive and procedurally simple new process that pairs acidic alumina with hexanes to achieve this important Michael
In situ generation of Iron(<scp>iii</scp>) dodecyl sulfate as Lewis acid-surfactant catalyst for synthesis of bis-indolyl, tris-indolyl, Di(bis-indolyl), Tri(bis-indolyl), tetra(bis-indolyl)methanes and 3-alkylated indole compounds in water
Iron(III) dodecyl sulfate as Lewis acid-surfactant catalyst was prepared in situ and effectively used in the synthesis of bis(indolyl)methanes and Michael reactions of indoles with α,β-unsaturated carbonyl compounds in water. Also, this method was used for the synthesis of 1,1,3-tri-indolyl compounds, producing good to excellent yield at room temperature.