The first example of oxidative C–H fluoroalkoxylation of quinoxalinones with fluoroalkyl
alcohols under transition-metal and solvent-free conditions is described. This approach …

Chalcones are a class of naturally occurring flavonoid compounds associated to a variety of
biological and pharmacological properties. Several reviews have been published describing …

Herein, we describe the development and application of a novel benzotriazole-based
reagent toward radical trifluoroethoxylation. Various alkene classes, including styrene …

Herein, we report a highly effective protocol for the cross-coupling of (hetero) aryl bromides
with fluorinated alcohols using the commercially available precatalyst tBuBrettPhos Pd G3 …

Fluorinated substances have outstanding importance in most fields of the chemical industry,
from agrochemicals and material science to pharmaceutical research. Although aryl‐and …

The synthesis of trifluoroethoxylated dihydropyrrolidones via rhodium-catalyzed oxidation
and trifluoroethoxylation of pyrrolidones is presented in this paper. This process realized the …

The trifluoroethyl aryl ethers are important motifs in drug molecules. However, a report
devoted specifically to the study of transition-metal-catalyzed C–H trifluoroethoxylation has …

A Cu-catalyzed cross-coupling reaction between aryl bromides and 9-BBN–OMe to provide
aryl methyl ethers under mild conditions is reported. The oxalamide ligand BHMPO plays a …

Copper-catalyzed oxidative trifluoroethoxylation of aryl boronic acids with CF3CH2OH -
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Herein, we report the metal-free synthesis of polyfluoroalkyl aryl ethers via nucleophilic
substitution of fluorosulfonates, obtained in one pot by bubbling of sulfuryl fluoride (SO2F2) …