Issue 39, 2019

Carbonyl and olefin hydrosilylation mediated by an air-stable phosphorus(iii) dication under mild conditions

Abstract

The readily-accessible, air-stable Lewis acid [(terpy)PPh][B(C6F5)4]21 is shown to mediate the hydrosilylation of aldehydes, ketones, and olefins. The utility and mechanism of these hydrosilylations are considered.

Graphical abstract: Carbonyl and olefin hydrosilylation mediated by an air-stable phosphorus(iii) dication under mild conditions

Supplementary files

Article information

Article type
Communication
Submitted
29 Mar 2019
Accepted
16 Apr 2019
First published
16 Apr 2019

Chem. Commun., 2019,55, 5599-5602

Carbonyl and olefin hydrosilylation mediated by an air-stable phosphorus(III) dication under mild conditions

R. J. Andrews, S. S. Chitnis and D. W. Stephan, Chem. Commun., 2019, 55, 5599 DOI: 10.1039/C9CC02460C

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