Issue 17, 2022

Grignard reagent formation via C–F bond activation: a centenary perspective

Abstract

Examples of Grignard reagents obtained by C–F bond activation with magnesium have kept appearing in the literature over the last century. Due to the high bond dissociation energy of the C–F bond, a lot of effort has been invested in the preparation of highly active forms of magnesium for this purpose. Originally, magnesium activation was achieved by the application of additives, notably iodine. Later work focused on the generation of highly active magnesium powder by reduction of magnesium salts with alkali metals (“Rieke magnesium”). Modern approaches to the problem involve the application of Mg(I)–Mg(I) dimers and C–F bond activation performed by a transition metal catalyst followed by transmetallation with a magnesium salt. The purpose of this article is to provide an overview of fluoro-Grignard reagent preparation approaches reported to date.

Graphical abstract: Grignard reagent formation via C–F bond activation: a centenary perspective

Article information

Article type
Feature Article
Submitted
01 Dec 2021
Accepted
06 Jan 2022
First published
06 Jan 2022

Chem. Commun., 2022,58, 2799-2813

Grignard reagent formation via C–F bond activation: a centenary perspective

E. Pietrasiak and E. Lee, Chem. Commun., 2022, 58, 2799 DOI: 10.1039/D1CC06753B

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