Litcius/Paper detail

Hydroxytrifluoroethylation and Trifluoroacetylation Reactions via SET Processes

Albert Gallego‐Gamo, Roser Pleixats, Carolina Gimbert‐Suriñach, Adelina Vallribera, Albert Granados

2024Chemistry - A European Journal17 citationsDOIOpen Access PDF

Abstract

Hydroxytrifluoroethyl and trifluoroacetyl groups are of utmost importance in biologically active compounds, but methods to tether these motifs to organic architectures have been limited. Typically, the preparation of these compounds relied on the use of strong bases or multistep routes. The renaissance of radical chemistry in photocatalytic, transition metal mediated, and hydrogen atom transfer (HAT) processes have allowed the installation of these medicinally relevant fluorinated motifs. This review provides an overview of the methods available for the direct synthesis of hydroxytrifluoroethyl- and trifluoroacetyl-derived compounds governed by single-electron transfer processes.

Topics & Concepts

The RenaissanceHydrogen atomChemistryCombinatorial chemistryElectron transferOrganic synthesisBiochemical engineeringOrganic chemistryCatalysisGroup (periodic table)EngineeringArt historyArtFluorine in Organic ChemistryRadical Photochemical ReactionsSulfur-Based Synthesis Techniques