Comprehensive Summary Sonogashira cross‐coupling protocol, typically showing the
reaction between aryl/vinyl halide and terminal alkyne, has been a widely used protocol for …

The importance of the quinoxaline framework is exemplified by its presence in the well-
known drugs such as varenicline, brimonidine, quinacillin, etc. In the past few years …

We have demonstrated that the T1-state energy of a fluorescence dopant (FD) is close to
that of the thermally activated delayed fluorescence (TADF)-type exciplex co-host, and the …

A new process has been developed for the bromine-promoted sequential (sp2) C=(sp2) C
bond functionalization of (E)-3-styrylquinoxalin-2 (1 H)-ones and furo [b] annulation via the 5 …

The thermally-activated delayed fluorescence (TADF)-sensitizing-fluorescence (TSF)
strategy suffers from a disturbing energy loss caused by the T1 states of the fluorescence …

A novel heavy metal‐free and safe synthetic methodology enabling one‐step conversion of
ketones into corresponding 4, 5, 6, 7‐tetrafluorobenzofurans (F4BFs) has been developed …

A facile, efficient, and simple one‐pot multi‐component protocol for the synthesis of pyrano
[2, 3‐c] pyrazoles has been developed using a cheap and readily available copper catalyst …

A tandem 6π-azacyclization approach for the synthesis of diversified pyrrolo/indolo [1, 2-a]
quinoxalines from amino-cyclopentenones has been developed. The reaction proceeds …

Unsymmetrical one-pot sequential cross-coupling reactions of sterically hindered
tetrabromothiophene with arylboronic acid and an alkyne/alkene to afford selective bi-, tri …

We have established a facile and versatile synthetic methodology for the construction of
tetrazoles and guanidines in the presence of an eco-friendly, inexpensive, easily available …