123736-03-8Relevant academic research and scientific papers
Copper-Catalyzed Conjugate Addition of Trialkylaluminium to α,β-Unsaturated Carbonyl Compounds
Kabbara, Jazid,Flemming, Steffen,Nickisch, Klaus,Neh, Harribert,Westermann, Juergen
, p. 743 - 754 (2007/10/02)
The Michael-type reaction of copper-catalyzed trialkylaluminium reagents with α,β-unsaturated carbonyl compounds is a useful and simple procedure for the transfer of hydrocarbon substituents.The scope of this process and the effect of chlorotrimethylsilane as additive were investigated.Preparatively useful results were generally obtainde from enones even with higher organoaluminium reagents, whereas the reaction with α,β-unsaturated aldehydes was limited to the use of trimethylaluminium.
CuX3Li2-catalysed Conjugate Addition of Dialkylmagnesium Reagents to α,β-Unsaturated Carbonyl Compounds
Reetz, Manfred T.,Kindler, Alois
, p. 2509 - 2510 (2007/10/02)
Copper salts of the type CuX3Li2 (X = halogen) catalyse the conjugate addition of dialkylmagnesium compounds to α,β-unsaturated carbonyl compounds in the presence or absence of Me3SiCl as an additive, the organomagnesium compounds being prepared from α-ol
