(Thio)urea Containing Chiral Ammonium Salt Catalysts
- PMID: 36175162
- DOI: 10.1002/tcr.202200198
(Thio)urea Containing Chiral Ammonium Salt Catalysts
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.
© 2022 The Authors. The Chemical Record published by The Chemical Society of Japan and Wiley-VCH GmbH.
References
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- For comprehensive overviews:
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- M. J. O'Donnell, in: Catalytic Asymmetric Syntheses, 2nd ed. (Ed: I. Ojima), Wiley-VCH, New York, 2000, pp. 727-755;
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- K. Maruoka (Ed.) Asymmetric Phase Transfer Catalysis, Wiley-VCH, Weinheim, 2008;
-
- M. R. Vitale, S. Oudeyer, V. Levacher, J. F. Brière, Radical and Ion-Pairing Strategies in Asymmetric Organocatalysis, Elsevier, 2017.
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- For selected reviews:
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