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Issue 4, 2018
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Catalytic asymmetric enamine protonation reaction

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Abstract

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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Article information


Submitted
24 Oct 2017
Accepted
16 Dec 2017
First published
18 Dec 2017

Org. Biomol. Chem., 2018,16, 510-520
Article type
Review Article

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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