A Sandmeyer-type difluoromethylation process has been developed that allows the straightforward conversion of (hetero-)arenediazonium salts into the corresponding difluoromethyl (hetero-)arenes under mild conditions. The actual difluoromethylating reagent, a difluoromethyl–copper complex, is formed in situ from copper thiocyanate and TMS–CF<sub>2</sub>H. The diazonium salts are either preformed or generated in situ from broadly available aromatic amines
The copper-catalyzed trifluoromethylthiolation of pyrroles with a trifluoromethanesulfonyl hype...
The use of TFEDMA, a fluoroalkyl amino reagent, for the difluoromethylation and difluoroacylation of...
A novel Cu-catalyzed <i>gem</i>-difluoroolefination of diazo compounds is described. This transforma...
A copper-promoted trifluoromethylation reaction of aromatic amines is described. This transformation...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A novel strategy for aromatic trifluoromethylation by converting aromatic amino group into CF3 group...
A palladium-catalyzed difluoromethylation of a series of heteroaryl chlorides, bromides and iodides ...
International audienceDifluoromethylated arenes are scaffolds of great interest. We report herein a ...
Treatment of propiolic acid amides with trifluoromethanesulfonic anhydride (Tf2O) leads to the forma...
Copper(I) trifluoromethanethiolate reacts with a range of diazonium salts containing electron-withdr...
The difluoromethyl group (CF2H) is of great interest in the area of medicinal chemistry. However, th...
The trifluoromethylation of carbonyl compounds is accomplished by the stable (trifluoromethyl)zinc r...
A means to trifluoromethylate: The beneficial properties imparted by the trifluoromethylation of aro...
Molecular scaffolds containing alkylfluorine substituents are desired in many areas of chemical rese...
The copper-catalyzed trifluoromethylthiolation of pyrroles with a trifluoromethanesulfonyl hype...
The use of TFEDMA, a fluoroalkyl amino reagent, for the difluoromethylation and difluoroacylation of...
A novel Cu-catalyzed <i>gem</i>-difluoroolefination of diazo compounds is described. This transforma...
A copper-promoted trifluoromethylation reaction of aromatic amines is described. This transformation...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A novel strategy for aromatic trifluoromethylation by converting amino into trifluoromethyl groups v...
A novel strategy for aromatic trifluoromethylation by converting aromatic amino group into CF3 group...
A palladium-catalyzed difluoromethylation of a series of heteroaryl chlorides, bromides and iodides ...
International audienceDifluoromethylated arenes are scaffolds of great interest. We report herein a ...
Treatment of propiolic acid amides with trifluoromethanesulfonic anhydride (Tf2O) leads to the forma...
Copper(I) trifluoromethanethiolate reacts with a range of diazonium salts containing electron-withdr...
The difluoromethyl group (CF2H) is of great interest in the area of medicinal chemistry. However, th...
The trifluoromethylation of carbonyl compounds is accomplished by the stable (trifluoromethyl)zinc r...
A means to trifluoromethylate: The beneficial properties imparted by the trifluoromethylation of aro...
Molecular scaffolds containing alkylfluorine substituents are desired in many areas of chemical rese...
The copper-catalyzed trifluoromethylthiolation of pyrroles with a trifluoromethanesulfonyl hype...
The use of TFEDMA, a fluoroalkyl amino reagent, for the difluoromethylation and difluoroacylation of...
A novel Cu-catalyzed <i>gem</i>-difluoroolefination of diazo compounds is described. This transforma...