Photoinduced chemical transformations have become a promising aspect of organic
synthesis. This review focuses on the recent advancements in harnessing photoinduced …

Aryl halides are one of the most important chemical feedstocks in pharmaceuticals due to its
easy accessibility, inexpensiveness, and widely utilized as aryl radical precursors in organic …

We have presented a carbonate anion assisted photochemical protocol for the C–X bond
activation. Anion− π interactions have been leveraged to generate aryl radicals from easily …

Preparation of S-aryl xanthates via transition-metal-catalyzed or SNAr reactions is
complicated by their further transformations under the utilized conditions. In contrast, S …

Contemporary methods for synthesizing thioesters often necessitate expensive catalysts and
harsh conditions, making their synthesis from chemical feedstocks challenging. Herein, we …

The development of effective strategies to forge C–O and C–S bonds in diverse chemical
spaces is of considerable interest in synthetic organic chemistry. Herein we report a versatile …

Nonsymmetric diarylethenes with an additional “stiff” cyclohexenol ring undergo various
types of tandem transformations launched by light-induced 6π-photocyclization. Among …

In the pharmaceutical sector, functionalized aryl sulfonamides are fundamental building
blocks. The photoexcitation of aryl (hetero) diazonium salts and sulfonamides enabled this …

A simple, efficient, and practical method for the synthesis of S-quinolyl xanthates was
developed via Ts2O-promoted deoxygenative C–H dithiocarbonation of quinoline N-oxides …

We have established a facile and efficient protocol for the generation of germyl radicals by
employing photo‐excited electron transfer (ET) in an electron donor‐acceptor (EDA) …