Literature DB >> 26577251

Kinetic Resolution of β-Sulfonyl Ketones through Enantioselective β-Elimination using a Cation-Binding Polyether Catalyst.

Liang Li1, Yidong Liu1, Yang Peng1, Lei Yu1, Xiaoyan Wu1, Hailong Yan2.   

Abstract

Reported herein is the first enantioselective β-elimination reaction catalyzed by a chiral cation-binding polyether. By using this catalytic protocol, a wide range of β-sulfonyl ketones could be effectively resolved with high stereoselectivity (S up to >300). Key to the success of this process is the favorable secondary interactions of the catalyst with the Lewis basic groups on the sulfone substrate. The enone product of this process can be easily converted into the racemic starting material, and allows an effective recycling and overall synthesis of chiral β-sulfonyl ketones in high yield and excellent enantioselectivity.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  asymmetric catalysis; ion pairs; kinetic resolution; organocatalysis; sulfones

Year:  2015        PMID: 26577251     DOI: 10.1002/anie.201508127

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


  3 in total

1.  Biomimetic catalytic transformation of toxic α-oxoaldehydes to high-value chiral α-hydroxythioesters using artificial glyoxalase I.

Authors:  Sang Yeon Park; In-Soo Hwang; Hyun-Ju Lee; Choong Eui Song
Journal:  Nat Commun       Date:  2017-04-04       Impact factor: 14.919

2.  Total synthesis of aristolactam alkaloids via synergistic C-H bond activation and dehydro-Diels-Alder reactions.

Authors:  Mallu Chenna Reddy; Masilamani Jeganmohan
Journal:  Chem Sci       Date:  2017-03-23       Impact factor: 9.825

3.  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 in total

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