Literature DB >> 29431882

Counterion-Induced Asymmetric Control in Ring-Opening of Azetidiniums: Facile Access to Chiral Amines.

Deyun Qian1,2, Min Chen1,2, Alex C Bissember3, Jianwei Sun1,2.   

Abstract

Counterion-induced stereocontrol is a powerful tool in organic synthesis. However, such enantiocontrol on tetrahedral ammonium cations remains challenging. Described here is the first example of using chiral anion phase-transfer catalysis to achieve intermolecular ring-opening of azetidiniums with excellent enantioselectivity (up to 97 % ee). Precise control over the formation and reaction of the chiral ion pair as well as inhibition of the background reaction by the biphasic system is key to the success of the reaction.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  asymmetric catalysis; chirality; organocatalysis; phase-transfer catalysis; small ring systems

Year:  2018        PMID: 29431882     DOI: 10.1002/anie.201712395

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  4 in total

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

Authors:  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
Journal:  J Am Chem Soc       Date:  2020-08-05       Impact factor: 15.419

2.  Hydrogen Bonding Phase-Transfer Catalysis with Alkali Metal Fluorides and Beyond.

Authors:  Gabriele Pupo; Véronique Gouverneur
Journal:  J Am Chem Soc       Date:  2022-03-16       Impact factor: 16.383

3.  Synthesis of optically active 2-substituted azetidine-2-carbonitriles from chiral 1-arylethylamine via α-alkylation of N-borane complexes.

Authors:  Eiji Tayama; Nobuhiro Nakanome
Journal:  RSC Adv       Date:  2021-07-06       Impact factor: 4.036

4.  Synthesis of tertiary alkyl fluorides and chlorides by site-selective nucleophilic ring-opening reaction of α-aryl azetidinium salts.

Authors:  Eiji Tayama; Kohei Kawai
Journal:  RSC Adv       Date:  2021-12-13       Impact factor: 3.361

  4 in total

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