Litcius/Paper detail

Hydrogen Bonding Phase-Transfer Catalysis with Ionic Reactants: Enantioselective Synthesis of γ-Fluoroamines

Giulia Roagna, David M. H. Ascough, Francesco Ibba, Anna Chiara Vicini, Alberto Fontana, Kirsten E. Christensen, Aldo Peschiulli, Daniel Oehlrich, Antonio Misale, Andrés A. Trabanco, Robert S. Paton, Gabriele Pupo, Véronique Gouverneur

2020Journal of the American Chemical Society75 citationsDOIOpen Access PDF

Abstract

-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.

Topics & Concepts

ChemistryEnantioselective synthesisCatalysisElectrophileReactivity (psychology)Hydrogen bondIonic bondingIonic liquidAlkali metalPhase (matter)DiastereomerRing (chemistry)Organic chemistryInorganic chemistryCombinatorial chemistryMoleculeIonAlternative medicinePathologyMedicineFluorine in Organic ChemistryInorganic Fluorides and Related CompoundsSynthesis and Reactions of Organic Compounds