Sulfonamides are key motifs in pharmaceuticals and agrochemicals, spurring the continuous development of novel and efficient synthetic methods to access these functional groups. Herein, we report an environmentally benign electrochemical method which enables the oxidative coupling between thiols and amines, two readily available and inexpensive commodity chemicals. The transformation is completely driven by electricity, does not require any sacrificial reagent or additional catalysts and can be carried out in only 5 min. Hydrogen is formed as a benign byproduct at the counter electrode. Owing to the mild reaction conditions, the reaction displays a broad substrate scope and functional group compatibility
The transfer of nitrogen atoms is extremely valuable in the preparation of medicinal compounds. Here...
We describe a method for the synthesis of sulfonamides through the combination of an organometallic ...
International audienceA sulfonylative Hiyama cross-coupling reaction using gaseous SO$_2$ is describ...
Sulfonamides are key motifs in pharmaceuticals and agrochemicals, spurring the continuous developmen...
Sulfonamides are key motifs in pharmaceuticals and agrochemicals, spurring the continuous developmen...
Sulfonamides are key motifs in pharmaceuticals and agrochemicals, spurring the continuous developmen...
Sulfonyl fluorides are valuable synthetic motifs for a variety of applications, among which sulfur(V...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...
Organosulfur compounds are being widely used in medicinal chemistry, as well as in organic transform...
Sulfonyl fluorides are valuable synthetic motifs which are currently of high interest due to the pop...
A transition metal-free strategy for the dehydrogenative β-sulfonylation of tertiary cyclic amines i...
NH-sulfoximines are emerging as useful and important targets in drug discovery and synthetic organic...
An efficient electrochemical flow process for the selective oxidation of sulfides to sulfoxides and ...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
The transfer of nitrogen atoms is extremely valuable in the preparation of medicinal compounds. Here...
We describe a method for the synthesis of sulfonamides through the combination of an organometallic ...
International audienceA sulfonylative Hiyama cross-coupling reaction using gaseous SO$_2$ is describ...
Sulfonamides are key motifs in pharmaceuticals and agrochemicals, spurring the continuous developmen...
Sulfonamides are key motifs in pharmaceuticals and agrochemicals, spurring the continuous developmen...
Sulfonamides are key motifs in pharmaceuticals and agrochemicals, spurring the continuous developmen...
Sulfonyl fluorides are valuable synthetic motifs for a variety of applications, among which sulfur(V...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...
Organosulfur compounds are being widely used in medicinal chemistry, as well as in organic transform...
Sulfonyl fluorides are valuable synthetic motifs which are currently of high interest due to the pop...
A transition metal-free strategy for the dehydrogenative β-sulfonylation of tertiary cyclic amines i...
NH-sulfoximines are emerging as useful and important targets in drug discovery and synthetic organic...
An efficient electrochemical flow process for the selective oxidation of sulfides to sulfoxides and ...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
The transfer of nitrogen atoms is extremely valuable in the preparation of medicinal compounds. Here...
We describe a method for the synthesis of sulfonamides through the combination of an organometallic ...
International audienceA sulfonylative Hiyama cross-coupling reaction using gaseous SO$_2$ is describ...