A simple and efficient tert-butyl hydroperoxide-mediated direct trifluoromethylation of indazoles using sodium trifluoromethanesulfinate has been developed under metal-free conditions. A library of trifluoromethylated products with broad functionalities has been synthesized with moderate to good yields. A radical mechanistic pathway has been proposed for the present protocol
We describe a simple, metal- and oxidantfree photochemical strategy for the direct trifluoromethylat...
ABSTRACT: The ability to convert simple and common substrates into fluoroalkyl derivatives under mil...
A highly efficient N-trifluoromethylation of nitro-soarenes is reported. The inexpensive and conveni...
A simple and efficient tert-butyl hydroperoxide-mediated direct trifluoromethylation of indazoles us...
Here we report a visible-light-promoted metal-free regioselective C3-H trifluoromehtylation reaction...
Trifluoromethyl-substituted heteroarenes are biologically active compounds and useful building block...
A metal-free and cost-effective synthesis protocol has been initially proposed for the construction ...
A mild and efficient method for the synthesis of 3-trifluoromethylpyrazoles has been established via...
Abed HB, Weissing N, Schoene J, Paulus J, Sewald N, Nazare M. Novel strategy for the preparation of ...
A novel and efficient cascade method has been developed for the diastereoselective preparation of tr...
A convenient approach for the construction of pharmaceutically valuable 3-trifluoromethyl-1,2,4-tria...
The first example of a copper(I)-catalyzed intramolecular aminotrifluoromethylation of unactivated ...
A simple and novel methodology for the synthesis of 3-perfluoroalkylated-2H-indazole derivatives has...
Electrophilic trifluoromethylation reactions have been the latest approach to achieve the fluoroalky...
An efficient, eco-compatible, and very cheap method for the construction of triazoles via eliminativ...
We describe a simple, metal- and oxidantfree photochemical strategy for the direct trifluoromethylat...
ABSTRACT: The ability to convert simple and common substrates into fluoroalkyl derivatives under mil...
A highly efficient N-trifluoromethylation of nitro-soarenes is reported. The inexpensive and conveni...
A simple and efficient tert-butyl hydroperoxide-mediated direct trifluoromethylation of indazoles us...
Here we report a visible-light-promoted metal-free regioselective C3-H trifluoromehtylation reaction...
Trifluoromethyl-substituted heteroarenes are biologically active compounds and useful building block...
A metal-free and cost-effective synthesis protocol has been initially proposed for the construction ...
A mild and efficient method for the synthesis of 3-trifluoromethylpyrazoles has been established via...
Abed HB, Weissing N, Schoene J, Paulus J, Sewald N, Nazare M. Novel strategy for the preparation of ...
A novel and efficient cascade method has been developed for the diastereoselective preparation of tr...
A convenient approach for the construction of pharmaceutically valuable 3-trifluoromethyl-1,2,4-tria...
The first example of a copper(I)-catalyzed intramolecular aminotrifluoromethylation of unactivated ...
A simple and novel methodology for the synthesis of 3-perfluoroalkylated-2H-indazole derivatives has...
Electrophilic trifluoromethylation reactions have been the latest approach to achieve the fluoroalky...
An efficient, eco-compatible, and very cheap method for the construction of triazoles via eliminativ...
We describe a simple, metal- and oxidantfree photochemical strategy for the direct trifluoromethylat...
ABSTRACT: The ability to convert simple and common substrates into fluoroalkyl derivatives under mil...
A highly efficient N-trifluoromethylation of nitro-soarenes is reported. The inexpensive and conveni...