Journal article

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


Authors listEschmann, C; Song, LJ; Schreiner, PR

Publication year2021

Pages4823-4832

JournalAngewandte Chemie International Edition

Volume number60

Issue number9

ISSN1433-7851

Open access statusGreen

DOI Linkhttps://doi.org/10.1002/anie.202012760

PublisherWiley


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.



Citation Styles

Harvard Citation styleEschmann, C., Song, L. and Schreiner, P. (2021) London Dispersion Interactions Rather than Steric Hindrance Determine the Enantioselectivity of the Corey-Bakshi-Shibata Reduction, Angewandte Chemie International Edition, 60(9), pp. 4823-4832. https://doi.org/10.1002/anie.202012760

APA Citation styleEschmann, C., Song, L., & Schreiner, P. (2021). London Dispersion Interactions Rather than Steric Hindrance Determine the Enantioselectivity of the Corey-Bakshi-Shibata Reduction. Angewandte Chemie International Edition. 60(9), 4823-4832. https://doi.org/10.1002/anie.202012760


Last updated on 2025-10-06 at 11:21