C–H activation has surfaced as an increasingly powerful tool for molecular sciences, with
notable applications to material sciences, crop protection, drug discovery, and …

This paper reviewed the recent research progress of organic reactions catalyzed by four
typical earth-abundant and 3d metal catalysts: Mn, Fe, Co, and Ni complexes and mainly …

Abstract Electrochemistry enabled C− H/N− H functionalizations at room temperature by
external oxidant‐free cobalt catalysis. Thus, the sustainable cobalt electrocatalysis manifold …

Electrochemical oxidative C–H/N–H activations have been accomplished with a versatile
cobalt catalyst in terms of [4+ 2] annulations of internal alkynes. The electro-oxidative C–H …

Considerable research attention has been directed towards the use of first‐row transition
metals in organic synthesis. The more abundant, and less expensive cobalt is considered to …

Expansion of the synthetic chemists' toolbox is currently a topic of great interest, with
successes providing access to novel compounds and more efficient routes towards new and …

Herein we describe the synthesis of a family of aryl-Co (III)-carboxylate complexes and their
reactivity with ethyl diazoacetate. Crystallographic, full spectroscopic characterization, and …

A method for cobalt‐catalyzed, carboxylate‐directed functionalization of arene C− H bonds
is reported. Alkynes, styrenes, and 1, 3‐dienes can be coupled with benzoic acids to provide …

A mechanistic understanding of electro-and photocatalytic CO2 reduction is crucial to
develop strategies to overcome catalytic bottlenecks. In this regard, for a new CO2-to-CO …

The merger of cobalt‐catalyzed C− H activation and electrosynthesis provides new avenues
for resource‐economical molecular syntheses, unfortunately their reaction mechanisms …