The site-selective C–H bond functionalization of heteroarenes can eventually provide
chemists with great techniques for editing and building complex molecular scaffolds. During …

Indole is one of the most important heterocycles in organic synthesis, natural products, and
drug discovery. Recently, tremendous advances in the selective functionalization of indoles …

Alkylation represents an important organic transformation in molecular science to develop
privileged alkylated arenes and heteroarenes. Especially, the direct C–H bond alkylation …

Transition-metal-catalyzed carbene transfer reactions, involving diazo compounds and their
precursors, are powerful tools for creating new C–C bonds. Depending on the involved …

Alkylated indoles are important motifs in various biologically active molecules and drug
candidates. Herein, we report a mild and efficient iron-catalyzed protocol for synthesizing …

Organometallic catalysts have played a key role in accomplishing numerous synthetically
valuable organic transformations that are either otherwise not possible or inefficient. The use …

Copper-catalyzed C–H functionalization is becoming a significant area in organic chemistry.
Copper is now widely used as a catalyst in organic synthesis as it is inexpensive and not …

Selective editing of the benzenoid C− H bonds (C4− C7) in indoles/indolines has received
great interest because functionalized indoles/indolines are featured in many marketed drugs …

Abstract C− H/C− H oxidative coupling has emerged as a straightforward and powerful
technique for the construction of (hetero) biaryls, with substantial application to drug …

Compared with non-ligated Ni–Al bimetallic catalysis, bifunctional ligand-ligated Ni–Al
bimetallic catalysis displays stronger synergism, not only affecting the electronic properties …