Potassium phosphate or silica sulfuric acid catalyzed conjugate addition of thiols to α, β-unsaturated ketones at room temperature under solvent-free conditions
Potassium phosphate and silica sulfuric acid have been found to be useful and highly efficient catalysts for conjugate addition of thiols to α, β-unsaturated ketones under solvent- free conditions, at room temperature. Silica sulfuric acid (SSA) was found to be suitable for electron-deficient enones while potassium phosphate was found to effect thia-Michael addition with both, electron-deficient as well as electron-rich conjugated ketones.
