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Issue 4, 2018
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Catalytic asymmetric enamine protonation reaction

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Enantioselective protonation, delivery of a proton to a carbanion intermediate, is the most straightforward and fundamental method for the preparation of a chiral tertiary carbon stereocenter. Recent efforts for this objective have been realized through enamine catalysis, which has now become a prominent catalytic strategy enabling a range of fascinating chiral transformations. This review will summarize recent advances in the field of enantioselective enamine protonation for the synthesis of optically active carbonyl compounds. Dynamic kinetic resolutions of α-substituted carbonyl compounds through enamine intermediates will be discussed as well.

Graphical abstract: Catalytic asymmetric enamine protonation reaction

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The article was received on 24 Oct 2017, accepted on 16 Dec 2017 and first published on 18 Dec 2017

Article type: Review Article
DOI: 10.1039/C7OB02615C
Citation: Org. Biomol. Chem., 2018,16, 510-520
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    Catalytic asymmetric enamine protonation reaction

    N. Fu, L. Zhang and S. Luo, Org. Biomol. Chem., 2018, 16, 510
    DOI: 10.1039/C7OB02615C

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