A highly efficient Rh-catalyzed carbenoid addition to trifluoromethylthioether for the formation of trifluoromethyl-substituted sulfonium ylide is described. The trifluoromethyl-substituted sulfonium ylide can act as an electrophilic trifluoromethylation reagent, as demonstrated by trifluoromethylation of β-ketoesters and aryl iodides
Sulfoxonium ylides have recently gained prominence as safe carbenoid precursors in metal-catalyzed r...
Methyltrioxorhenium acts as a catalyst (5–10 mol %) for the direct electrophilic trifluoromethylatio...
A convenient strategy for the synthesis of sulfur ylides via rhodium-catalyzed coupling of in situ g...
A highly efficient Rh-catalyzed carbenoid addition to trifluoromethylthioether for the formation o...
Sulfoxonium ylides act as an efficient carbene precursor in rhodium(III)-catalyzed C–H acylmethlyat...
The intra- vs intermolecular transfer-fluoromethylation of aryl fluoromethylthio compounds is propos...
The trifluoromethylthio (SCF3) functional group has been of increasing importance in drug design and...
A novel electrophilic-type trifluoromethylthiolation reagent, a trifluoromethanesulfonyl hypervalent...
[2,3]-Sigmatropic rearrangement of sulfonium ylide generated through metal carbene and sulfide is kn...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
Sulfoxonium ylides have recently gained prominence as safe carbenoid precursors in metal-catalyzed r...
Methyltrioxorhenium acts as a catalyst (5–10 mol %) for the direct electrophilic trifluoromethylatio...
A convenient strategy for the synthesis of sulfur ylides via rhodium-catalyzed coupling of in situ g...
A highly efficient Rh-catalyzed carbenoid addition to trifluoromethylthioether for the formation o...
Sulfoxonium ylides act as an efficient carbene precursor in rhodium(III)-catalyzed C–H acylmethlyat...
The intra- vs intermolecular transfer-fluoromethylation of aryl fluoromethylthio compounds is propos...
The trifluoromethylthio (SCF3) functional group has been of increasing importance in drug design and...
A novel electrophilic-type trifluoromethylthiolation reagent, a trifluoromethanesulfonyl hypervalent...
[2,3]-Sigmatropic rearrangement of sulfonium ylide generated through metal carbene and sulfide is kn...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
International audienceA general method for the α-trifluoromethylthiolation of carbonyl compounds, wi...
Sulfoxonium ylides have recently gained prominence as safe carbenoid precursors in metal-catalyzed r...
Methyltrioxorhenium acts as a catalyst (5–10 mol %) for the direct electrophilic trifluoromethylatio...
A convenient strategy for the synthesis of sulfur ylides via rhodium-catalyzed coupling of in situ g...