Issue 46, 2021

Mechanistic investigations of alcohol silylation with isothiourea catalysts

Abstract

The mechanism of the asymmetric silylation of alcohols with isothiourea catalysts was studied by employing reaction progress kinetic analysis. These reactions were developed by the Wiskur group, and use triphenyl silyl chloride and chiral isothiourea catalysts to silylate the alcohols. While the order of most reaction components was as expected (catalyst, amine base, alcohol), the silyl chloride was determined to be a higher order. This suggested a multistep mechanism between the catalyst and silyl chloride, with the second equivalent of silyl chloride assisting in the formation of the reactive intermediate leading to the rate-determining step. Through the addition of additives and investigating changes in the silyl chloride, an understanding of the catalyst equilibrium emerged for this reaction and provided pathways for further reaction development.

Graphical abstract: Mechanistic investigations of alcohol silylation with isothiourea catalysts

Supplementary files

Article information

Article type
Paper
Submitted
03 Sep 2021
Accepted
04 Nov 2021
First published
17 Nov 2021

Org. Biomol. Chem., 2021,19, 10181-10188

Author version available

Mechanistic investigations of alcohol silylation with isothiourea catalysts

B. K. Redden, R. W. Clark, Z. Gong, Md. M. Rahman, D. V. Peryshkov and S. L. Wiskur, Org. Biomol. Chem., 2021, 19, 10181 DOI: 10.1039/D1OB01732B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements