Trifluoroethylarenes are found in a variety of biologically active molecules, and strategies for accessing this substructure are important for developing therapeutic candidates and biological probes. Trifluoroethylarenes can be directly accessed via nucleophilic trifluoromethylation of benzylic electrophiles; however, current catalytic methods do not effectively transform electron-deficient substrates and heterocycles. To address this gap, we report a Cu-catalyzed decarboxylative trifluoromethylation of benzylic bromodifluoroacetates. To account for the tolerance of sensitive functional groups, we propose an inner-sphere mechanism of decarboxylation
“Cu–CF3” species have been used historically for a broad spectrum of nucleophilic trifluoromethylati...
“Cu–CF3” species have been used historically for a broad spectrum of nucleophilic trifluoromethylati...
Trifluoromethylated acetylenes and arenes are widely applicable in the synthesis of pharmaceuticals ...
Trifluoroethylarenes are found in a variety of biologically active molecules, and strategies for acc...
Trifluoromethanes play an important role in medicinal chemistry, and methods that enable the rapid s...
Trifluoromethanes play an important role in medicinal chemistry, and methods that enable the rapid s...
The development of efficient methods for accessing fluorinated functional groups is desirable. Herei...
The development of efficient methods for accessing fluorinated functional groups is desirable. Herei...
The development of new synthetic fluorination reactions has important implications in medicinal, agr...
The development of new synthetic fluorination reactions has important implications in medicinal, agr...
Compared with the prefunctionalized substrates in traditional cross-coupling reactions, carboxylic a...
Compared with the prefunctionalized substrates in traditional cross-coupling reactions, carboxylic a...
Compared with the prefunctionalized substrates in traditional cross-coupling reactions, carboxylic a...
ABSTRACT: The ability to convert simple and common substrates into fluoroalkyl derivatives under mil...
Abstract A Cu-mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TM...
“Cu–CF3” species have been used historically for a broad spectrum of nucleophilic trifluoromethylati...
“Cu–CF3” species have been used historically for a broad spectrum of nucleophilic trifluoromethylati...
Trifluoromethylated acetylenes and arenes are widely applicable in the synthesis of pharmaceuticals ...
Trifluoroethylarenes are found in a variety of biologically active molecules, and strategies for acc...
Trifluoromethanes play an important role in medicinal chemistry, and methods that enable the rapid s...
Trifluoromethanes play an important role in medicinal chemistry, and methods that enable the rapid s...
The development of efficient methods for accessing fluorinated functional groups is desirable. Herei...
The development of efficient methods for accessing fluorinated functional groups is desirable. Herei...
The development of new synthetic fluorination reactions has important implications in medicinal, agr...
The development of new synthetic fluorination reactions has important implications in medicinal, agr...
Compared with the prefunctionalized substrates in traditional cross-coupling reactions, carboxylic a...
Compared with the prefunctionalized substrates in traditional cross-coupling reactions, carboxylic a...
Compared with the prefunctionalized substrates in traditional cross-coupling reactions, carboxylic a...
ABSTRACT: The ability to convert simple and common substrates into fluoroalkyl derivatives under mil...
Abstract A Cu-mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TM...
“Cu–CF3” species have been used historically for a broad spectrum of nucleophilic trifluoromethylati...
“Cu–CF3” species have been used historically for a broad spectrum of nucleophilic trifluoromethylati...
Trifluoromethylated acetylenes and arenes are widely applicable in the synthesis of pharmaceuticals ...