A Pd-catalyzed three component reaction involving terminal alkynes, boronic acids, and perfluoroalkyl iodides is presented here. Trisubstituted perfluoroalkenes can be obtained in a highly regio- and stereocontrolled manner by the simultaneous addition of both aryl and CnFm groups across the triple bond in a radical-mediated process. The reaction is operationally simple offering a broad scope and functional group tolerance
Alkene difunctionalization featuring an intramolecular carbometallation step has been developed into...
The site-selective palladium-catalyzed three-component coupling of deactivated alkenes, arylboronic ...
We describe a new catalytic approach to selective functionalization of the strong C–F bonds in trifl...
A Pd-catalyzed difunctionalization of internal alkynes combining boronic acids and perfluoroalkyl io...
A Pd-catalyzed difunctionalization of internal alkynes combining boronic acids and perfluoroalkyl io...
A Pd-catalyzed anti-stereospecific alkyne fluoroalkylboration, including mono-, di-, and perfluoroal...
A palladium-catalyzed aryldifluoroalkylation of alkynes with ethyl difluoroiodoacetate and arylboron...
A novel, four-component synthetic strategy to synthesize a series of β<i>-</i>difluoroalkyl unsatura...
A novel, four-component synthetic strategy to synthesize a series of β<i>-</i>difluoroalkyl unsatura...
An efficient C<sub>sp</sub>–CH<sub>2</sub>CF<sub>3</sub> bond-forming reaction via Pd-catalyzed 2,2,...
A method for regio- and stereoselective anti-addition of the perfluoroalkyl and the triflate group o...
A four-component Pd-catalyzed protocol for direct synthesis of perfluoroalkyl-substituted enones is ...
A trifluoroethylation of alkynes through a palladium-catalyzed decarboxylative coupling reaction was...
A novel protocol for palladium-catalyzed fluoroarylation of 1,1-difluoroallenes was described here. ...
The control of a reaction that can form multiple products is a highly attractive and challenging con...
Alkene difunctionalization featuring an intramolecular carbometallation step has been developed into...
The site-selective palladium-catalyzed three-component coupling of deactivated alkenes, arylboronic ...
We describe a new catalytic approach to selective functionalization of the strong C–F bonds in trifl...
A Pd-catalyzed difunctionalization of internal alkynes combining boronic acids and perfluoroalkyl io...
A Pd-catalyzed difunctionalization of internal alkynes combining boronic acids and perfluoroalkyl io...
A Pd-catalyzed anti-stereospecific alkyne fluoroalkylboration, including mono-, di-, and perfluoroal...
A palladium-catalyzed aryldifluoroalkylation of alkynes with ethyl difluoroiodoacetate and arylboron...
A novel, four-component synthetic strategy to synthesize a series of β<i>-</i>difluoroalkyl unsatura...
A novel, four-component synthetic strategy to synthesize a series of β<i>-</i>difluoroalkyl unsatura...
An efficient C<sub>sp</sub>–CH<sub>2</sub>CF<sub>3</sub> bond-forming reaction via Pd-catalyzed 2,2,...
A method for regio- and stereoselective anti-addition of the perfluoroalkyl and the triflate group o...
A four-component Pd-catalyzed protocol for direct synthesis of perfluoroalkyl-substituted enones is ...
A trifluoroethylation of alkynes through a palladium-catalyzed decarboxylative coupling reaction was...
A novel protocol for palladium-catalyzed fluoroarylation of 1,1-difluoroallenes was described here. ...
The control of a reaction that can form multiple products is a highly attractive and challenging con...
Alkene difunctionalization featuring an intramolecular carbometallation step has been developed into...
The site-selective palladium-catalyzed three-component coupling of deactivated alkenes, arylboronic ...
We describe a new catalytic approach to selective functionalization of the strong C–F bonds in trifl...