38266-46-5Relevant articles and documents
Highly efficient Michael addition reaction of amines catalyzed by silica-supported aluminum chloride
Saidi, Mohammad R.,Pourshojaei, Yaghoub,Aryanasab, Fezzeh
experimental part, p. 1109 - 1119 (2009/09/08)
Aliphatic and aromatic amines undergo smooth nucleophilic addition to α,β-unsaturated compounds in the presence of a catalytic amount of silica-supported aluminum chloride at 60°C and under solvent-free conditions to produce the corresponding β-amino compounds in excellent yields. This method is simple and convenient and works efficiently under mild conditions. This catalyst can used again without losing its activity three times. Copyright Taylor & Francis Group, LLC.