Transition metal-free C-3 functionalization of quinoxalin-2 (1H)-ones has recently emerged
as a modern sustainable protocol, as C-3 functionalized quinoxalin-2 (1H)-ones offer robust …

The first piezochemically driven decarboxylative coupling of the C–H bond was developed.
The agitation of BaTiO3 via ball milling converts mechanical energy into electrical potential …

Visible light promoted eosin Y catalyzed selective C3-H acylation of quinoxalin-2 (1H)-ones
has been developed in a green and sustainable manner. In contrast to the conventional …

A visible-light-induced chemoselective reactions of quinoxalin-2 (1 H)-ones with
alkylboronic acids in the presence of air (O 2) and N 2 atmosphere was developed under …

A visible light-promoted radical relay of N-allylbromodifluoroacetamide with quinoxalin-2 (1
H)-ones was developed in which 5-exo-trig cyclization and C–C bond formation were …

A visible‐light‐promoted synthesis of quinoxalin‐2 (1H)‐ones has been developed using 9‐
mesityl‐10‐methylacridinium perchlorate as an organo‐photocatalyst. The atmosphere …

Organic synthesis involves the production of important chemical structures using scalable
and cost‐effective methods that are also environmentally friendly. In this review, a detailed …

With aldehydes as the radical precursors under visible-light irradiation, a simple and mild C–
H acylation reaction of quinoxalin-2 (1H)-ones has been achieved. A wide variety of …

A sunlight-promoted sulfenylation of quinoxalin-2 (1 H)-ones using recyclable graphitic
carbon nitride (g-C3N4) as a heterogeneous photocatalyst was developed. Using the …

A practical and efficient methodology for the construction of 3-alkylquinoxalinones through
base promoted direct alkylation of quinoxalin-2 (1H)-ones with phosphonium ylides as …