Issue 72, 2018

Enantioselective acyl-transfer catalysis by fluoride ions

Abstract

The asymmetric nucleophilic catalysis by fluoride ions at a carbon-based electrophile has been demonstrated for the first time. Using a library of ad hoc designed bifunctional phase-transfer catalysts in which both the anion and the cation are directly involved in the reaction, the desymmetrisation of meso-succinic and -glutaric anhydrides is possible. 19F NMR spectroscopic studies support the intermediacy of an acyl fluoride intermediate.

Graphical abstract: Enantioselective acyl-transfer catalysis by fluoride ions

Supplementary files

Article information

Article type
Communication
Submitted
13 juil. 2018
Accepted
13 août 2018
First published
20 août 2018

Chem. Commun., 2018,54, 10108-10111

Enantioselective acyl-transfer catalysis by fluoride ions

R. Craig, M. Litvajova, S. A. Cronin and S. J. Connon, Chem. Commun., 2018, 54, 10108 DOI: 10.1039/C8CC05692G

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