Journalartikel
Autorenliste: Eschmann, C; Song, LJ; Schreiner, PR
Jahr der Veröffentlichung: 2021
Seiten: 4823-4832
Zeitschrift: Angewandte Chemie International Edition
Bandnummer: 60
Heftnummer: 9
ISSN: 1433-7851
Open Access Status: Green
DOI Link: https://doi.org/10.1002/anie.202012760
Verlag: Wiley
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-Zitierstil: Eschmann, 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-Zitierstil: Eschmann, 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