The generation of sulfonyl radicals from sulfonyl azides using visible light and a photoactive iridium complex in THF is described. This process was used to promote sulfonylative and azidosulfonylative cyclizations of enynes to give several classes of highly functionalized heterocycles. The use of THF as the solvent is critical for successful reactions. The proposed mechanism of radical initiation involves the photosensitized formation of a triplet sulfonyl nitrene, which abstracts a hydrogen atom from THF to give a tetrahydrofuran-2-yl radical, which then reacts with the sulfonyl azide to generate the sulfonyl radical
Sulfinamides have widespread applications in organic synthesis, especially for the preparation of S(...
The authors thank the European Research Council under the European Union’s Seventh Framework Program...
To date, nitrogen-centered radicals (NCRs) and sulfur(VI)-centered radicals have received increasing...
The generation of sulfonyl radicals from sulfonyl azides using visible light and a photoactive iridi...
N′-Benzylidene-N-homoallylacetohydrazides were designed and synthesized as novel skeletons for the c...
A highly diastereoselective, visible-light-induced [3 + 2] cycloaddition between N-sulfonyl cyclopro...
A synthetically useful Z-selective cascade formal thiyl radical addition, 1,3-double bond isomerizat...
A plethora of drug molecules and agrochemicals contain the sulfonamide functional group. However, su...
This thesis presents various photocatalytic approaches towards the preparation of the pharmaceutical...
We here have developed an S(O)2–N coupling between phenylsulfinic acid derivatives and aryl azides b...
Recent advances in radical azidation using sulfonyl azides are presented. For instance, radical carb...
The radical azidoalkylation of alkenes that was initially developed with α-iodoesters and α-iodoketo...
Alkyl radicals are obtained by photocatalytic oxidation of readily prepared or commercially availabl...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
An iodine-promoted one-pot radical cyclization reaction of 1,6-enynes with sulfonyl hydrazides to pr...
Sulfinamides have widespread applications in organic synthesis, especially for the preparation of S(...
The authors thank the European Research Council under the European Union’s Seventh Framework Program...
To date, nitrogen-centered radicals (NCRs) and sulfur(VI)-centered radicals have received increasing...
The generation of sulfonyl radicals from sulfonyl azides using visible light and a photoactive iridi...
N′-Benzylidene-N-homoallylacetohydrazides were designed and synthesized as novel skeletons for the c...
A highly diastereoselective, visible-light-induced [3 + 2] cycloaddition between N-sulfonyl cyclopro...
A synthetically useful Z-selective cascade formal thiyl radical addition, 1,3-double bond isomerizat...
A plethora of drug molecules and agrochemicals contain the sulfonamide functional group. However, su...
This thesis presents various photocatalytic approaches towards the preparation of the pharmaceutical...
We here have developed an S(O)2–N coupling between phenylsulfinic acid derivatives and aryl azides b...
Recent advances in radical azidation using sulfonyl azides are presented. For instance, radical carb...
The radical azidoalkylation of alkenes that was initially developed with α-iodoesters and α-iodoketo...
Alkyl radicals are obtained by photocatalytic oxidation of readily prepared or commercially availabl...
Photo-sensitized synthesis of arylsulfides from arenediazonium salts in the presence of eosin Y has ...
An iodine-promoted one-pot radical cyclization reaction of 1,6-enynes with sulfonyl hydrazides to pr...
Sulfinamides have widespread applications in organic synthesis, especially for the preparation of S(...
The authors thank the European Research Council under the European Union’s Seventh Framework Program...
To date, nitrogen-centered radicals (NCRs) and sulfur(VI)-centered radicals have received increasing...