An efficient method for the direct C(sp)–H difluoromethylation of terminal alkynes and the desilylation–difluoromethylation of (trimethylsilyl)acetylenes is disclosed. The copper-catalyzed transformation provides access to a wide range of structurally diverse CF2H alkynes in good yields, utilizing a (difluoromethyl)zinc reagent and an organic oxidant. The difluoromethylation of important synthons and API’s is showcased. The synthetic utility of these (difluoromethyl)alkynes is demonstrated by selected cycloaddition reactions. Additionally, a slight modification to the reaction conditions allowed the selective preparation of a 2-difluoromethylindole
An efficient and selective hydro-trifluoromethylation of terminal alkynes is developed to enable the...
The title reaction proceeds with acetylenic triflones and isocyanides under mild conditions using co...
The difluoromethylation of terminal alkynes through the use of fluoroform as a source of difluorocar...
International audienceBased on a Castro–Stephens transformation, a coupling reaction between copper ...
International audienceBased on a Castro–Stephens transformation, a coupling reaction between copper ...
International audienceBased on a Castro–Stephens transformation, a coupling reaction between copper ...
Trifluoromethylated acetylenes and arenes are widely applicable in the synthesis of pharmaceuticals ...
A general and facile synthetic method for C(sp<sup>2</sup>)–H difluoroalkylations and perfluoroalky...
Two practical and complementary methods are reported for the synthesis of trifluoromethylated alkyne...
International audienceThe introduction of a double or triple bond to the nitrogen atom of S-perfluor...
International audienceThe introduction of a double or triple bond to the nitrogen atom of S-perfluor...
International audienceThe introduction of a double or triple bond to the nitrogen atom of S-perfluor...
International audienceThe introduction of a double or triple bond to the nitrogen atom of S-perfluor...
The difluoromethyl group (CF2H) is of great importance in medicinal chemistry. We report herein an e...
An efficient oxydifluoroalkylation of hydroxyl-containing alkenes using a copper catalytic system ha...
An efficient and selective hydro-trifluoromethylation of terminal alkynes is developed to enable the...
The title reaction proceeds with acetylenic triflones and isocyanides under mild conditions using co...
The difluoromethylation of terminal alkynes through the use of fluoroform as a source of difluorocar...
International audienceBased on a Castro–Stephens transformation, a coupling reaction between copper ...
International audienceBased on a Castro–Stephens transformation, a coupling reaction between copper ...
International audienceBased on a Castro–Stephens transformation, a coupling reaction between copper ...
Trifluoromethylated acetylenes and arenes are widely applicable in the synthesis of pharmaceuticals ...
A general and facile synthetic method for C(sp<sup>2</sup>)–H difluoroalkylations and perfluoroalky...
Two practical and complementary methods are reported for the synthesis of trifluoromethylated alkyne...
International audienceThe introduction of a double or triple bond to the nitrogen atom of S-perfluor...
International audienceThe introduction of a double or triple bond to the nitrogen atom of S-perfluor...
International audienceThe introduction of a double or triple bond to the nitrogen atom of S-perfluor...
International audienceThe introduction of a double or triple bond to the nitrogen atom of S-perfluor...
The difluoromethyl group (CF2H) is of great importance in medicinal chemistry. We report herein an e...
An efficient oxydifluoroalkylation of hydroxyl-containing alkenes using a copper catalytic system ha...
An efficient and selective hydro-trifluoromethylation of terminal alkynes is developed to enable the...
The title reaction proceeds with acetylenic triflones and isocyanides under mild conditions using co...
The difluoromethylation of terminal alkynes through the use of fluoroform as a source of difluorocar...