Issue 4, 2019

Chemistry of detrifluoroacetylatively in situ generated fluoro-enolates

Abstract

This review article comprehensively profiles all literature reports (2015–2018) related to the detrifluoroacetylative in situ generation of fluorine-containing enolates and their reactions with electrophilic reagents. The innovative facets of this unconventional methodology and its synthetic generality for the preparation of fluorine-containing compounds of high medicinal value are highlighted.

Graphical abstract: Chemistry of detrifluoroacetylatively in situ generated fluoro-enolates

Article information

Article type
Review Article
Submitted
15 Nov 2018
Accepted
13 Dis 2018
First published
13 Dis 2018

Org. Biomol. Chem., 2019,17, 762-775

Chemistry of detrifluoroacetylatively in situ generated fluoro-enolates

H. Mei, J. Liu, S. Fustero, R. Román, R. Ruzziconi, V. A. Soloshonok and J. Han, Org. Biomol. Chem., 2019, 17, 762 DOI: 10.1039/C8OB02843E

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