Quinoxalines, a class of N-heterocyclic compounds, are important biological agents, and a
significant amount of research activity has been directed towards this class. They have …

Nucleophilic aromatic substitution (SNAr) is a class of reaction that has become very
important over time. This type of transformation usually proceeds without the use of metal …

The quinoxaline scaffold is a promising platform for the discovery of active chemotherapeutic
agents. Three series of quinoxaline derivatives were synthesized and biologically evaluated …

A new series of 2, 4-disubstituted thiazole derivatives containing 4-(3, 4, 5-trimethoxyphenyl)
moiety was synthesized and evaluated for their potential anticancer activity as tubulin …

A novel, simple and practical method for the regioselective halogenation of fused
heterocyclic N-oxides has been developed. It employs Vilsmeier reagent, generated in situ …

To shed light on the significance of thiazole derivatives in the advancement of cancer
medication and to contribute to therapeutic innovation, we have designed the synthesis and …

The COVID-19 pandemic represents a substantial global challenge, being a significant
cause of mortality in numerous countries. Thus, it is imperative to conduct research to …

In this paper, we report the successful synthesis of new 2-phenyl-3-substituted furo/thieno [2,
3-b] quinoxaline derivatives from 2-chloro-3-methoxyquinoxaline and 2-chloro-3 …

A convenient, one-pot multi-component synthesis of new 2, 4-disubstituted hydrazinyl-
thiazoles was accomplished using different aldehydes/ketones, thiosemicarbazide, and 4 …

An efficient one‐pot reaction has been developed for the synthesis of 2, 3‐
dichloroquinoxaline derivatives 3a–n. The reaction was performed in two steps via a silica …