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Review
. 2023 Jul;23(7):e202200198.
doi: 10.1002/tcr.202200198. Epub 2022 Sep 29.

(Thio)urea Containing Chiral Ammonium Salt Catalysts

Affiliations
Review

(Thio)urea Containing Chiral Ammonium Salt Catalysts

Mario Waser et al. Chem Rec. 2023 Jul.

Abstract

(Thio)-urea-containing bifunctional quaternary ammonium salts emerged as powerful non-covalently interacting organocatalysts over the course of the last decade. The most commonly employed catalysts in this field are either based on Cinchona alkaloids, α-amino acids, or trans-cyclohexane-1,2-diamine. Our group has been heavily engaged in the design and use of such catalysts, i. e. trans-cyclohexane-1,2-diamine-based ones for around 10 years now, and it is therefore the intention of this short personal account to provide an overview of the, at least in our opinion, most significant and pioneering achievements in this field by looking on catalyst design and asymmetric method development, with a special focus on our own contributions.

Keywords: (thio)-ureas; H-bonding; asymmetric organocatalysis; ion pairing catalysis; quaternary ammonium salts.

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References

    1. For comprehensive overviews:
    1. M. J. O'Donnell, in: Catalytic Asymmetric Syntheses, 2nd ed. (Ed: I. Ojima), Wiley-VCH, New York, 2000, pp. 727-755;
    1. K. Maruoka (Ed.) Asymmetric Phase Transfer Catalysis, Wiley-VCH, Weinheim, 2008;
    1. M. R. Vitale, S. Oudeyer, V. Levacher, J. F. Brière, Radical and Ion-Pairing Strategies in Asymmetric Organocatalysis, Elsevier, 2017.
    1. For selected reviews:

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