Journalartikel

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


AutorenlisteEschmann, C; Song, LJ; Schreiner, PR

Jahr der Veröffentlichung2021

Seiten4823-4832

ZeitschriftAngewandte Chemie International Edition

Bandnummer60

Heftnummer9

ISSN1433-7851

Open Access StatusGreen

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

VerlagWiley


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.



Zitierstile

Harvard-ZitierstilEschmann, 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-ZitierstilEschmann, 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



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