Trifluoromethylated acetylenes and arenes are widely applicable in the synthesis of pharmaceuticals and agrochemicals. In 2010, our group has reported the copper-mediated oxidative trifluomethylation of terminal alkynes and aryl boronic acids. This method allows a wide range of functional group tolerant trifluoromethylated acetylenes and arenes to be easily prepared. After the preliminary mechanistic studies of the oxidative trifluoromethylation of terminal alkyne, an efficient copper-catalyzed oxidative trifluoromethylation of terminal alkynes and aryl boronic acids has been developed. The catalytic protocol is successfully achieved by adding both the substrate and a portion of CF<sub>3</sub>TMS slowly using a syringe pump to the reaction ...
This article describes the copper-catalyzed oxidative trifluoromethylation of heteroarenes and highl...
The introduction of trifluoromethyl groups into organic molecules has attracted great attention in t...
The development of new synthetic fluorination reactions has important implications in medicinal, agr...
Two practical and complementary methods are reported for the synthesis of trifluoromethylated alkyne...
An efficient method for the copper-catalyzed trifluoromethylation of terminal alkenes with an electr...
An efficient method for the direct C(sp)–H difluoromethylation of terminal alkynes and the desilylat...
A novel copper-catalyzed intermolecular trifluoromethylarylation of alkenes is developed using l...
Copper-mediated trifluoromethylation of unsaturated organotrifluoroborates with the Langlois reagent...
An efficient C(sp<sup>3</sup>)–CF<sub>3</sub> bond-forming reaction via Cu-catalyzed oxidative trifl...
An efficient and synthetically convenient method for copper-catalyzed cross-coupling of aryl boronic...
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...
This thesis concerns the use of various potent oxidants in organic synthesis. The main focus is dire...
This thesis concerns the use of various potent oxidants in organic synthesis. The main focus is dire...
A method for the room temperature copper-mediated trifluoromethylation of aryl and heteroaryl boroni...
This article describes the copper-catalyzed oxidative trifluoromethylation of heteroarenes and highl...
The introduction of trifluoromethyl groups into organic molecules has attracted great attention in t...
The development of new synthetic fluorination reactions has important implications in medicinal, agr...
Two practical and complementary methods are reported for the synthesis of trifluoromethylated alkyne...
An efficient method for the copper-catalyzed trifluoromethylation of terminal alkenes with an electr...
An efficient method for the direct C(sp)–H difluoromethylation of terminal alkynes and the desilylat...
A novel copper-catalyzed intermolecular trifluoromethylarylation of alkenes is developed using l...
Copper-mediated trifluoromethylation of unsaturated organotrifluoroborates with the Langlois reagent...
An efficient C(sp<sup>3</sup>)–CF<sub>3</sub> bond-forming reaction via Cu-catalyzed oxidative trifl...
An efficient and synthetically convenient method for copper-catalyzed cross-coupling of aryl boronic...
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...
This thesis concerns the use of various potent oxidants in organic synthesis. The main focus is dire...
This thesis concerns the use of various potent oxidants in organic synthesis. The main focus is dire...
A method for the room temperature copper-mediated trifluoromethylation of aryl and heteroaryl boroni...
This article describes the copper-catalyzed oxidative trifluoromethylation of heteroarenes and highl...
The introduction of trifluoromethyl groups into organic molecules has attracted great attention in t...
The development of new synthetic fluorination reactions has important implications in medicinal, agr...