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Asymmetric Michael addition of malonates to enones catalyzed by a siloxy amino acid lithium salt
Authors:Masanori Yoshida  Mao Narita  Keisuke Hirama  Shoji Hara
Affiliation:Division of Chemical Process Engineering, Graduate School of Engineering, Hokkaido University, Sapporo 060-8628, Japan
Abstract:Siloxy amino acid lithium salt, O-tert-butyldiphenylsilyl l-serine lithium salt, was found to be an effective catalyst for the asymmetric Michael addition reaction of malonates to enones.
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