The multicomponent reactions of quinoxalin‐2 (1H)‐ones has attracted considerable interest
due to their significant biological and chemical activities. The very recent advances (from …

The direct C–H multifunctionalization of quinoxalin-2 (1 H)-ones via multicomponent
reactions has attracted considerable interest due to their diverse biological activities and …

A mild and efficient photochemical multi-component tandem reaction of quinoxalin-2 (1 H)-
ones, alkenes and sulfinic acids is reported. This tandem reaction could be conveniently …

An environmentally friendly strategy for the photocatalyzed three-component reaction
between quinoxalinones, alkenes, and hypervalent iodine (III) reagents is disclosed. The …

The incorporation of sulfonyl fluoride groups into molecules has been proved effective to
enhance their biological activities or introduce new functions. Herein, we report a transition …

The key significance of the radical cascade process is the ease of building complex organic
frameworks. As a result, introducing pharmaceutically important heterocycles to cascade …

A photoredox-catalyzed strategy for difunctionalization of alkenes with readily available
quinoxalin-2 (1H)-ones and inexpensive ICH2CF3/ICH2CF2H was developed. This reaction …

A strategy to synthesize 3‐alkyl quinoxalin‐2 (1H)‐ones and other alkyl N‐heteroarenes via
a photocatalyzed decarbonylative alkylation of quinoxalin‐2 (1H)‐ones and simple N …

A metal‐free multi‐component sulfur dioxide insertion reaction of alkynes, sodium
metabisulfite, aryldiazonium, and quinoxalin‐2‐ones has been developed under visible …

A novel sulfonyl radical triggered selective iodosulfonylation and bicyclization of 1, 6-dienes
has been described for the first time. High selectivity and efficiency, mild reaction conditions …