An oxidative annulation of N-arylbenzimidamides with maleimides has been developed for
the first time using a catalytic amount of the [Cp* RhCl2] 2 complex for the synthesis of a …

Over the decades, functionalized heteroaromatic compounds and their scaffolds have drawn
significant attention in synthetic organic chemistry as well as in interdisciplinary sciences …

Regioselectively arylated heteroarenes are privileged scaffolds with remarkable biological
and optoelectronic properties. Traditional arylation approaches based on the transition …

A Ru (II)-catalyzed regioselective direct ortho-amidation of 2-aryl benzo [d] thiazoles
employing acyl azides as a nitrogen source has been accomplished. This approach utilizes …

The necessary use of large amounts of a homogeneous electrolyte represents a major issue
and challenge for the whole sustainability of electrosynthetic procedures. Herein, we report …

A protocol for carbene insertion into the inert C (sp2)–H bond has been established wherein
β-carbolines and isoquinolines are explored as intrinsic directing groups. The Ru (II) …

Abstract Citral (1a), a bioactive component of Cymbopogon citratus (lemongrass) could be
isolated and semi‐synthetic analogs synthesized with improved therapeutic properties …

In this study, an efficient method for the synthesis of benzoxazoles by coupling catechols,
aldehydes and ammonium acetate using ZrCl4 as catalyst in ethanol is reported. A wide …

An efficient metal-free synthesis strategy of benzoxazoles was developed via coupling
catechols, ammonium acetate, and alkenes/alkynes/ketones. The developed methodology …

The site-selective functionalization of aromatic compounds via C–H activation has emerged
as a popular tool in organic synthesis. In this study, we report a regioselective coupling of …