A visible-light-induced annulation/thiolation of 2-isocyanobiaryls with dialkyl(aryl)disulfides has been established, delivering a sustainable and atom-economic route to 6-organoylthiophenanthridines with wild functional group tolerance and good to excellent yields under oxidant-, base-, and transition-metal-free conditions
Synthetically useful radical thiol–ene reactions can be initiated by visible-light irradiation in th...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...
Aryl borates lie at the heart of carbon–carbon bond couplings, and they are widely applied to the sy...
A mild, efficient and straightforward visible-light-driven method has been developed to construct 1,...
We report a visible light responsive moiety capable of generating highly reactive thioaldehydes. Upo...
An efficient protocol for visible-light-mediated synthesis of a specific class of 1,2,4-dithiazolidi...
A metal-free visible-light-promoted oxidative coupling between thiols and arylhydrazines has been de...
Disclosed is a mild, scalable, visible-light-promoted cross-coupling reaction between thiols and ary...
The general catalytic synthesis of aryl and vinyl thioethers from readily available halides remains ...
We introduce a highly efficient ligation system based on a visible light-induced rearrangement affor...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
Metal-free oxidative radical 1,2-alkylarylation of unactivated alkenes with the α-C(sp3)–H bond of ...
The development of a mild, atom- and step-economical catalytic strategy that effectively generates v...
A metal-free photoredox C–H alkylation of heteroaromatics from readily available carboxylic acids us...
183-191An efficient synthesis of diheteroaryl sulphides has been achieved by visible light photocata...
Synthetically useful radical thiol–ene reactions can be initiated by visible-light irradiation in th...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...
Aryl borates lie at the heart of carbon–carbon bond couplings, and they are widely applied to the sy...
A mild, efficient and straightforward visible-light-driven method has been developed to construct 1,...
We report a visible light responsive moiety capable of generating highly reactive thioaldehydes. Upo...
An efficient protocol for visible-light-mediated synthesis of a specific class of 1,2,4-dithiazolidi...
A metal-free visible-light-promoted oxidative coupling between thiols and arylhydrazines has been de...
Disclosed is a mild, scalable, visible-light-promoted cross-coupling reaction between thiols and ary...
The general catalytic synthesis of aryl and vinyl thioethers from readily available halides remains ...
We introduce a highly efficient ligation system based on a visible light-induced rearrangement affor...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
Metal-free oxidative radical 1,2-alkylarylation of unactivated alkenes with the α-C(sp3)–H bond of ...
The development of a mild, atom- and step-economical catalytic strategy that effectively generates v...
A metal-free photoredox C–H alkylation of heteroaromatics from readily available carboxylic acids us...
183-191An efficient synthesis of diheteroaryl sulphides has been achieved by visible light photocata...
Synthetically useful radical thiol–ene reactions can be initiated by visible-light irradiation in th...
The metal‐free activation of C(sp3)‐H bonds to value‐added products is of paramount importance in or...
Aryl borates lie at the heart of carbon–carbon bond couplings, and they are widely applied to the sy...