1204199-72-3Relevant academic research and scientific papers
CuCl-catalyzed stereoselective conjugate addition of Grignard reagents to 2,3-allenoates
He, Jian,Lu, Zhan,Chai, Guobi,Fu, Chunling,Ma, Shengming
experimental part, p. 2719 - 2724 (2012/04/18)
CuCl was found to be an efficient catalyst for the conjugate addition of 2,3-allenoates with Grignard reagents to synthesize poly-substituted β,γ-unsaturated alkenoates with high stereoselectivity in good to excellent yields. Primary, secondary, and terti
Ferric chloride hexahydrate-catalyzed highly regio- And stereoselective conjugate addition reaction of 2,3-allenoates with grignard reagents: An efficient synthesis of β,γ-alkenoates
Chai, Guobi,Lu, Zhan,Fu, Chunling,Ma, Shengming
supporting information; experimental part, p. 1946 - 1954 (2011/02/26)
Ferric chloride hexahydrate was shown to be an efficient catalyst for the conjugate addition of 2,3-allenoates with alkyl-, aryl-, or vinyl-Grignard reagents to synthesize polysubstituted β,γ-unsaturated alkenoates with high regio- and stereoselectivity.
