Issue 29, 2021

Bifunctional squaramide catalyzed asymmetric synthesis of chiral α-mercaptosilanes

Abstract

Bifunctional squaramide-catalyzed nucleophilic addition of thiophenols to easily available β-silyl α,β-unsaturated carbonyl compounds has been successfully developed. A structurally diverse set of chiral α-mercaptosilanes was efficiently prepared in good to excellent yields with acceptable enantioselectivities. The reaction features mild reaction conditions, a broad substrate scope, and easy scale-up.

Graphical abstract: Bifunctional squaramide catalyzed asymmetric synthesis of chiral α-mercaptosilanes

Supplementary files

Article information

Article type
Communication
Submitted
20 May 2021
Accepted
29 Jun 2021
First published
29 Jun 2021

Org. Biomol. Chem., 2021,19, 6412-6416

Bifunctional squaramide catalyzed asymmetric synthesis of chiral α-mercaptosilanes

Y. Zhang, J. Guo, J. Han, X. Zhou, W. Cao and Z. Fu, Org. Biomol. Chem., 2021, 19, 6412 DOI: 10.1039/D1OB00981H

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