Triazene is one of the most versatile building blocks in organic synthesis. Generally, it is
viewed as a safe equivalent of diazonium salt, thus immediately finding numerous …

Aryltriazenes have emerged as very useful and versatile building blocks in organic synthesis
due to their easy preparation, good stability, multiple reaction sites and mild reaction …

Visible-Light-Induced Photocatalytic Oxidative Decarboxylation of Cinnamic Acids to 1,2-Diketones
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A photo‐induced direct arylation of quinoxalin‐2 (1H)‐ones with aryltriazenes under catalyst‐
free and ambient conditions was developed. The synthetic importance of this methodology …

Abstract Libraries of diaryl‐1, 2‐diketones were synthesized by oxidative coupling of 1‐aryl‐
ethynes with 1‐aryl‐triazenes, employing tetramethylguanidinium ionic liquid …

An I2-mediated approach for selective C–H functionalization of unprotected aniline
derivatives for synthesizing benzils and quinoxaline derivatives from sulfoxonium ylides has …

The bifunctional Lewis acidic ionic liquid (LAIL) catalyzed multicomponent arylsulfonation of
phenols with aryl triazenes and DABSO was developed. By using LAILs as redox and Lewis …

A new ruthenium/dendrimer complex stabilized on the surface of silica‐functionalized nano‐
magnetite was fabricated and well characterized. The nano‐catalyst showed good activity in …

A metal‐free, efficient and environmentally benign protocol for the synthesis of aryldiazo
sulfones from aryltriazenes and sodium aryl/alkyl sulfinates is described. The procedure …

Abstract The 1, 2‐diketone structural motif is present in various natural products and
compounds of biological significance. In addition, these compounds are frequently used as …