A mild, efficient and straightforward visible-light-driven method has been developed to construct 1,2-diarylvinyl sulfides under catalyst- and additive-free conditions. The formation of small amounts of thiyl radicals under visible light irradiation allows the synthesis of 1,2-diarylvinyl sulfides in good yield with an excellent functional group tolerance
We introduce a highly efficient ligation system based on a visible light-induced rearrangement affor...
International audienceAlkyne hydrothiolation – that is, the addition of the SH bond of a thiol acros...
Electron-rich arenes react with aryl and alkyl disulfides in the presence of catalytic amounts of [I...
A mild, efficient and straightforward visible-light-driven method has been developed to construct 1,...
Without any additives and photocatalysts, the visible-light-promoted radical cascade reaction betwee...
The general catalytic synthesis of aryl and vinyl thioethers from readily available halides remains ...
A synthetically useful Z-selective cascade formal thiyl radical addition, 1,3-double bond isomerizat...
An associative electron upconversion is proposed as a key step determining the selectivity of thiol–...
Herein, we have developed a new method for the synthesis of ((methyl-d3)sulfonyl)ethyne, which is co...
A metal-free visible-light-promoted oxidative coupling between thiols and arylhydrazines has been de...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
A mild and practical method for the preparation of disulfides through visible-light-induced photocat...
Herein, a one-step chlorosulfonylation of alkynes via a photocatalytic redox process is described. A...
© 2022 American Chemical Society. All rights reserved.Herein, we report a regioselective visible-lig...
A thiol-alkynylation procedure utilizing the hypervalent iodine alkyne transfer reagent TIPS-ethynyl...
We introduce a highly efficient ligation system based on a visible light-induced rearrangement affor...
International audienceAlkyne hydrothiolation – that is, the addition of the SH bond of a thiol acros...
Electron-rich arenes react with aryl and alkyl disulfides in the presence of catalytic amounts of [I...
A mild, efficient and straightforward visible-light-driven method has been developed to construct 1,...
Without any additives and photocatalysts, the visible-light-promoted radical cascade reaction betwee...
The general catalytic synthesis of aryl and vinyl thioethers from readily available halides remains ...
A synthetically useful Z-selective cascade formal thiyl radical addition, 1,3-double bond isomerizat...
An associative electron upconversion is proposed as a key step determining the selectivity of thiol–...
Herein, we have developed a new method for the synthesis of ((methyl-d3)sulfonyl)ethyne, which is co...
A metal-free visible-light-promoted oxidative coupling between thiols and arylhydrazines has been de...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
A mild and practical method for the preparation of disulfides through visible-light-induced photocat...
Herein, a one-step chlorosulfonylation of alkynes via a photocatalytic redox process is described. A...
© 2022 American Chemical Society. All rights reserved.Herein, we report a regioselective visible-lig...
A thiol-alkynylation procedure utilizing the hypervalent iodine alkyne transfer reagent TIPS-ethynyl...
We introduce a highly efficient ligation system based on a visible light-induced rearrangement affor...
International audienceAlkyne hydrothiolation – that is, the addition of the SH bond of a thiol acros...
Electron-rich arenes react with aryl and alkyl disulfides in the presence of catalytic amounts of [I...