Asymmetric Michael addition of malonates to enones catalyzed by a siloxy amino acid lithium salt |
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Authors: | Masanori Yoshida Mao Narita Keisuke Hirama Shoji Hara |
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Affiliation: | Division of Chemical Process Engineering, Graduate School of Engineering, Hokkaido University, Sapporo 060-8628, Japan |
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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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