Quinoxalines, also known as benzo [a] pyrazines, constitute an important class of nitrogen-
containing heterocyclic compounds as a result of their widespread prevalence in natural …

The oxa-Pictet–Spengler reaction is arguably the most straightforward and modular way to
construct the privileged isochroman motif, but its scope is largely limited to benzaldehyde …

Divergent deaminative and denitrative C–N cleavages and cascade transformations using
amines and nitroalkanes have been developed under a highly effective and environmentally …

A new method for directly synthesizing acylated and alkylated quinazoline derivatives by the
epoxide ring-opening reaction in the presence of I2/DMSO with 2-aminobenzamide is …

An acid-functionalized ionic liquid (IL)-catalyzed cascade decarboxylative cyclization of 2-
arylanilines with α-oxocarboxylic acids was developed. This approach offered a sustainable …

A metal-free, peroxide-free, and efficient procedure for the highly selective synthesis of
quinolines and methylquinolines was reported. The main feature of this method was that the …

The synthesis of pyrrolo [1, 2-α] quinoxalines is of importance, because they possess a
variety of biological activities, and interesting fluorescence/photophysical properties …

A catalytic domino reduction–imine formation–intramolecular cyclization–oxidation for the
general synthesis of a wide variety of biologically relevant N‐polyheterocycles, such as …

An array of pyrrolo [1, 2-a] quinoxaline derivatives were achieved with moderate to good
yields via the electrochemical redox reaction, which includes the functionalization of C (sp3) …

A quinazolin-4 (3 H)-one ring system is a privileged heterocyclic moiety with distinctive
biological properties. From this perspective, the development of an efficient strategy for the …