An efficient and highly selective approach for intermolecular arylthiocyanation/arylselenocyanation of alkenes has been reported under mild conditions. Using diazonium salts as the arylating agent and ammonium thiocyanate as the thiocyanate source, chemoselective difunctionalization of alkenes has been done under irradiation of visible light. Both styrenes and acrylates work well to deliver various aryl-substituted alkylthiocyanates in good to excellent yields. In addition, hitherto unknown β-aryl alkylselenocyanates were also synthesized using the developed protocol with potassium selenocyanate
The photoactivation of electron donor-acceptor (EDA) complexes has emerged as a sustainable, selecti...
Activated by visible light, arylazo sulfones can serve as multifaceted reactants and are employed in...
In the modern era of chemistry, photoredox catalysis has proven its usefulness in many synthetic app...
An efficient and highly selective approach for intermolecular arylthiocyanation/arylselenocyanation ...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
Introducing aryl- and heteroaryl moieties into molecular scaffolds are often key steps in the synthe...
Organophotocatalyzed three-component 1,2-difluoroacetyl/alkyl/perfluoroalkylative thio/selenocyanati...
Simultaneous sulfonylation/arylation of styrene derivatives is achieved in a photoredox-catalyzed th...
N-Bromosulphonamides, synthesized via direct bromination of sulphonamides, react with several types ...
International audienceTransition metal-catalyzed C-H bond functionalizations have been the focus of ...
The visible light induced C–H bond thiocyanation on the α-site of tertiary enaminones has been reali...
Eosin-Y (EY)-mediated alkylsulfonyl cyanation of olefins was shown to afford alkylsulfonyl nitriles ...
A visible light mediated, metal-free process for the thiocyanation of imidazoheterocycles has been d...
Acyl radicals were smoothly generated from acylsilanes under photoredoxcatalyzed conditions. These r...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
The photoactivation of electron donor-acceptor (EDA) complexes has emerged as a sustainable, selecti...
Activated by visible light, arylazo sulfones can serve as multifaceted reactants and are employed in...
In the modern era of chemistry, photoredox catalysis has proven its usefulness in many synthetic app...
An efficient and highly selective approach for intermolecular arylthiocyanation/arylselenocyanation ...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
Introducing aryl- and heteroaryl moieties into molecular scaffolds are often key steps in the synthe...
Organophotocatalyzed three-component 1,2-difluoroacetyl/alkyl/perfluoroalkylative thio/selenocyanati...
Simultaneous sulfonylation/arylation of styrene derivatives is achieved in a photoredox-catalyzed th...
N-Bromosulphonamides, synthesized via direct bromination of sulphonamides, react with several types ...
International audienceTransition metal-catalyzed C-H bond functionalizations have been the focus of ...
The visible light induced C–H bond thiocyanation on the α-site of tertiary enaminones has been reali...
Eosin-Y (EY)-mediated alkylsulfonyl cyanation of olefins was shown to afford alkylsulfonyl nitriles ...
A visible light mediated, metal-free process for the thiocyanation of imidazoheterocycles has been d...
Acyl radicals were smoothly generated from acylsilanes under photoredoxcatalyzed conditions. These r...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
The photoactivation of electron donor-acceptor (EDA) complexes has emerged as a sustainable, selecti...
Activated by visible light, arylazo sulfones can serve as multifaceted reactants and are employed in...
In the modern era of chemistry, photoredox catalysis has proven its usefulness in many synthetic app...