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 11 2018
Accepted
13 12 2018
First published
13 12 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

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