Since the 1950s, diaryliodonium (III) salts have been demonstrated to participate in various
arylation reactions, forming aryl–heteroatom and aryl–carbon bonds. Incorporating the …

Fused tetracyclic systems containing a quinoline nucleus represent an important class of
heterocyclic bioactive natural products and pharmaceuticals because of their significant and …

This account aims to give a description of the usefulness of diaryliodonium salts in organic
chemistry, including their synthesis and applications in the presence and absence of …

P‐stereogenic compounds are widely used as ligands in asymmetric catalysis and are
present in a myriad of bioactive compounds and pharmaceuticals. Yet, their stereocontrolled …

A three-component cascade cyclization catalyzed by copper was employed to synthesize
quinoline-4-thiols using easily available diaryliodonium salts, alkynyl sulfides, and nitriles as …

The structural motif of chromeno [4, 3-b] pyridine can be found in a wide variety of
pharmaceuticals and bioactive compounds. In this study, we have synthesized 2-(4, 5-di-p …

An efficient and concise one-pot procedure was developed based on a cascade reaction of
3-formylchromones 1 and different types of 1, 1-enediamines (EDAMs) 2 with different …

An efficient and rapid synthesis of multiply substituted quinolines is described. This method
is enabled by a three-component cascade annulation of readily available aryl diazonium …

Developing versatile methodologies to construct various nitrogen-containing heterocycles is
a crucially significant part of contemporary organic chemistry. This review summarizes …

A copper-catalyzed regiocontrolled three-component reaction afforded diversified 4-
aminoquinolines using nitriles, diaryliodoniums, and ynamides. The C7-substituted …