Conspectus Electrochemistry has been used as a tool to drive chemical reactions for over
two centuries. With the help of an electrode and a power source, chemists are bestowed with …

In recent years, radical C–C bond cleavage reactions have been increasingly understood
and used to perform transformations that complement traditional ionic processes. However …

Vicinal diamines, especially unsymmetrical ones, are among the most common structural
motifs in biologically active molecules, natural products and pharmaceuticals. While the …

The 1, 2-diamine motif is prevalent in natural products, small-molecule pharmaceuticals, and
catalysts for asymmetric synthesis. Transition metal catalyzed alkene diazidation has …

Vicinal diamines are a common structural motif in bioactive natural products, therapeutic
agents, and molecular catalysts, motivating the continuing development of efficient …

Given its many distinct characteristics, electrochemistry represents an attractive approach to
meet the prevailing trends in organic synthesis. In particular, electrocatalysis—a process that …

Despite the extensive applications, selective and diverse access to N, N′-diarylethane-1, 2-
diamines remains, to date, a challenge. Here, by developing a bifunctional cobalt single …

Vicinal diamines are privileged synthetic motifs in chemistry due to their prevalence and
powerful applications in bioactive molecules, pharmaceuticals, and ligand design for …

Inspired by the need for green and sustainable chemistry,(1) synthetic chemists seek more
efficient ways to construct carbon− carbon (C− C) bonds, the essential link in all organic …

Transition-metal-catalyzed remote hydrofunctionalization of alkenes remains an efficient but
challenging protocol in chemical synthesis. Herein, we reported a ligand-controlled …