Asymmetric Direct Michael Addition of Acetophenone to α,β-Unsaturated Aldehydes
Wenjun Li, Wenbin Wu, Juanjuan Yang, Xinmiao Liang, Jinxing Ye*
*Engineering Research Centre of Pharmaceutical Process Chemistry, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. of China, Email: yejxecust.edu.cn
W. Li, W. Wu, J. Yang, X. Liang, J. Ye, Synthesis, 2011, 1085-1091.
DOI: 10.1055/s-0030-1258459
see article for more reactions
Abstract
An asymmetric direct Michael addition of α,β-unsaturated aldehydes with acetophenone catalyzed by a Jørgensen-Hayashi catalyst in methanol gave δ-keto aldehydes in up to 82% yield and 98% ee.
see article for more examples
Key Words
1,5-Diketones, Michael Addition, Organocatalysis, Asymmetric Catalysis, Ketones, Aldehydes, Enals
ID: J66-Y2011-0920