Literature DB >> 33205853

London Dispersion Interactions Rather than Steric Hindrance Determine the Enantioselectivity of the Corey-Bakshi-Shibata Reduction.

Christian Eschmann1, Lijuan Song1,2, Peter R Schreiner1.   

Abstract

The well-known Corey-Bakshi-Shibata (CBS) reduction is a powerful method for the asymmetric synthesis of alcohols from prochiral ketones, often featuring high yields and excellent selectivities. While steric repulsion has been regarded as the key director of the observed high enantioselectivity for many years, we show that London dispersion (LD) interactions are at least as important for enantiodiscrimination. We exemplify this through a combination of detailed computational and experimental studies for a series of modified CBS catalysts equipped with dispersion energy donors (DEDs) in the catalysts and the substrates. Our results demonstrate that attractive LD interactions between the catalyst and the substrate, rather than steric repulsion, determine the selectivity. As a key outcome of our study, we were able to improve the catalyst design for some challenging CBS reductions.
© 2020 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.

Entities:  

Keywords:  CBS reduction; asymmetric catalysis; borane reduction; noncovalent interactions; steric repulsion

Year:  2021        PMID: 33205853     DOI: 10.1002/anie.202012760

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


  8 in total

1.  Kinetic Analysis of a Cysteine-Derived Thiyl-Catalyzed Asymmetric Vinylcyclopropane Cycloaddition Reflects Numerous Attractive Noncovalent Interactions.

Authors:  Amanda K Turek; Marcus H Sak; Scott J Miller
Journal:  J Am Chem Soc       Date:  2021-09-23       Impact factor: 16.383

2.  Noncovalent CH-π and π-π Interactions in Phosphoramidite Palladium(II) Complexes with Strong Conformational Preference.

Authors:  Matej Žabka; Lavakumar Naviri; Ruth M Gschwind
Journal:  Angew Chem Int Ed Engl       Date:  2021-11-03       Impact factor: 16.823

3.  Hydrogen Atom Transfer Driven Enantioselective Minisci Reaction of Alcohols.

Authors:  Avene C Colgan; Rupert S J Proctor; David C Gibson; Padon Chuentragool; Antti S K Lahdenperä; Kristaps Ermanis; Robert J Phipps
Journal:  Angew Chem Int Ed Engl       Date:  2022-04-27       Impact factor: 16.823

4.  An induced-fit model for asymmetric organocatalytic reactions: a case study of the activation of olefins via chiral Brønsted acid catalysts.

Authors:  Ingolf Harden; Frank Neese; Giovanni Bistoni
Journal:  Chem Sci       Date:  2022-07-04       Impact factor: 9.969

5.  London Dispersion Favors Sterically Hindered Diarylthiourea Conformers in Solution.

Authors:  Lars Rummel; Marvin H J Domanski; Heike Hausmann; Jonathan Becker; Peter R Schreiner
Journal:  Angew Chem Int Ed Engl       Date:  2022-06-14       Impact factor: 16.823

6.  Deployment of Sulfinimines in Charge-Accelerated Sulfonium Rearrangement Enables a Surrogate Asymmetric Mannich Reaction.

Authors:  Minghao Feng; Ivan Mosiagin; Daniel Kaiser; Boris Maryasin; Nuno Maulide
Journal:  J Am Chem Soc       Date:  2022-07-15       Impact factor: 16.383

7.  Extension of an Atom-Atom Dispersion Function to Halogen Bonds and Its Use for Rational Design of Drugs and Biocatalysts.

Authors:  Wiktoria Jedwabny; Edyta Dyguda-Kazimierowicz; Katarzyna Pernal; Krzysztof Szalewicz; Konrad Patkowski
Journal:  J Phys Chem A       Date:  2021-02-23       Impact factor: 2.781

8.  Computational Investigation on the Origin of Atroposelectivity for the Cinchona Alkaloid Primary Amine-Catalyzed Vinylogous Desymmetrization of N-(2-t-Butylphenyl)maleimides.

Authors:  Nicolò Tampellini; Paolo Righi; Giorgio Bencivenni
Journal:  J Org Chem       Date:  2021-08-04       Impact factor: 4.354

  8 in total

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