Symmetry 2011, 3(2), 155-164; doi:10.3390/sym3020155
Article

Primary Amino Acid Lithium Salt-Catalyzed Asymmetric Michael Addition of Carbon Nucleophiles to Enones

Received: 18 February 2011; in revised form: 6 April 2011 / Accepted: 7 April 2011 / Published: 8 April 2011
(This article belongs to the Special Issue Asymmetric Organocatalysis)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Asymmetric Michael addition of carbon nucleophiles, nitroalkanes and a β-ketoester, to enones was investigated by using a primary amino acid lithium salt as a catalyst.
Keywords: amino acid; asymmetric synthesis; organocatalysis; michael addition
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MDPI and ACS Style

Yoshida, M.; Hirama, K.; Narita, M.; Hara, S. Primary Amino Acid Lithium Salt-Catalyzed Asymmetric Michael Addition of Carbon Nucleophiles to Enones. Symmetry 2011, 3, 155-164.

AMA Style

Yoshida M, Hirama K, Narita M, Hara S. Primary Amino Acid Lithium Salt-Catalyzed Asymmetric Michael Addition of Carbon Nucleophiles to Enones. Symmetry. 2011; 3(2):155-164.

Chicago/Turabian Style

Yoshida, Masanori; Hirama, Keisuke; Narita, Mao; Hara, Shoji. 2011. "Primary Amino Acid Lithium Salt-Catalyzed Asymmetric Michael Addition of Carbon Nucleophiles to Enones." Symmetry 3, no. 2: 155-164.

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