Carbon–sulfur bond cross-coupling has become more and more attractive as an alternative
protocol to establish carbon–carbon and carbon–heteroatom bonds. Diverse …

Heterocyclic compounds are considered to be one of the most established structural classes
due to their extensive application in agrochemicals, pharmaceuticals and organic materials …

Sulfonamides are among the most important chemical motifs in pharmaceuticals and
agrochemicals. However, there is no methodology to directly introduce the sulfonamide …

The first electrochemical dehydrogenative C− S bond formation leading to thienoacene
derivatives is described. Several thienoacene derivatives were synthesized by …

An electrochemical method has been developed to achieve the C3-thiolation of quinoline
compounds. Achievements of this new strategy included maximum atom economy, direct …

Recently, sulphur containing molecules have witnessed significant recognition due to their
wide application in various fields. In this regard, the synthesis of such C− S containing …

Monofluoroalkenes are stable and lipophilic amide bioisosteres used in medicinal
chemistry. However, efficient and stereoselective methods for synthesizing Z …

We report the development of an isothiouronium salt as a reagent for the operationally
simple synthesis of cyanomethyl thioesters with high functional group tolerance and …

An effective and proficient process for the synthesis of a variety of thioethers via the one‐
step reaction of benzyl halides, aryl halides, and thiourea is presented. This strategy is a one …

A continuous flow metal‐free protocol for the synthesis of sulfonyl chlorides from thiols and
disulfides in the presence of nitric acid, hydrochloric acid and oxygen was developed. The …