Achieving high molecular complexity can be not trivial, but the exploitation of domino
reactions provides an atom‐and step‐economical method to reach this target. Over the past …

Abstract Site‐selective C (sp3)− H functionalization of unreactive hydrocarbons is always
challenging due to its inherited chemical inertness, slightly different reactivity of various C …

A mild and eco-friendly visible-light-induced protocol for the hydroacylation of quinones with
α-keto acids has been developed. In the absence of any catalyst or additive, the …

A visible‐light induced approach has enabled the synthesis of 3‐alkyl indole from ynones
via Csp3− H bond functionalization. This protocol proceeded under base‐free conditions …

Pnictogens, classified within group 15 elements, play a pivotal role in the constitution of a
diverse array of drug molecules, natural products, and functional materials. Recent research …

A simple one-pot domino protocol has been demonstrated for cascade trifluoromethyl-
amination/sulfoximination of quinones using a Gold (I) catalyzed multicomponent strategy …

A novel eco‐friendly methodology for the synthesis of 3‐selanylindoles has been
established, circumventing the requirement for transition metal catalysis, strong oxidants and …

A facile, efficient, and practical method for copper-catalyzed direct amination of maleimides
and quinones with formamides in the presence of an oxidant KIO 3 has been developed. It …

The direct functionalization of quinones has always fascinated research communities due to
their biological and redox activities and subsequent application. Quinone motifs play a vital …

This article proposes a milder approach for C (sp2=− H functionalization of 2, 2‐disubstituted
cyclopentene‐1, 3‐dione via formal 1° amination utilizing water as a solvent. In addition, this …