1. Hydrogen bonding phase-transfer catalysis with ionic reactants: enantioselective synthesis of γ-fluoroamines
- Author
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Kirsten E. Christensen, David M. H. Ascough, Alberto Fontana, Giulia Roagna, Gabriele Pupo, Anna Chiara Vicini, Andrés A. Trabanco, Francesco Ibba, Antonio Misale, Aldo Peschiulli, Robert S. Paton, Daniel Oehlrich, and Véronique Gouverneur
- Subjects
Chemistry ,Hydrogen bond ,Communication ,Diastereomer ,Enantioselective synthesis ,Ionic bonding ,General Chemistry ,010402 general chemistry ,Alkali metal ,01 natural sciences ,Biochemistry ,Combinatorial chemistry ,Catalysis ,0104 chemical sciences ,Colloid and Surface Chemistry ,Electrophile ,Reactivity (chemistry) - Abstract
Ammonium salts are used as phase-transfer catalysts for fluorination with alkali metal fluorides. We now demonstrate that these organic salts, specifically azetidinium triflates, are suitable substrates for enantioselective ring opening with CsF and a chiral bis-urea catalyst. This process, which highlights the ability of hydrogen bonding phase-transfer catalysts to couple two ionic reactants, affords enantioenriched γ-fluoroamines in high yields. Mechanistic studies underline the role of the catalyst for phase-transfer, and computed transition state structures account for the enantioconvergence observed for mixtures of achiral azetidinium diastereomers. The N-substituents in the electrophile influence the reactivity, but the configuration at nitrogen is unimportant for the enantioselectivity.
- Published
- 2020
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