Conspectus Transition metal-catalyzed carbonylation reactions represent a direct and atom-
economical approach to introduce oxygen functionality into organic compounds, with CO …

Transition metal-catalysed cross-coupling reactions are widely used for construction of
carbon–carbon and carbon–heteroatom bonds. However, compared to aryl or alkenyl …

An unprecedented straightforward reductive amidation of chloroalkanes with nitroarenes
was readily accomplished by merging iron catalysis with visible-light photoredox catalysis. A …

The direct catalytic reductive functionalization of nitroarenes to produce amines with
enhanced properties continues to attract attention for both academic and industrial …

Acid anhydrides are valuable in the chemical industry for their role in synthesizing polymers,
pharmaceuticals, and other commodities, but their syntheses often involve multiple steps …

We herein developed a reductive transamidation reaction between N-acyl benzotriazoles
(AcBt) and organic nitro compounds or NaNO2 under mild conditions. This protocol …

A unique and practical molybdenum-mediated reductive deuteration of nitroarenes for the
selective synthesis of ortho-and para-deuterated anilines has been developed. Using Mo …

We present here a metal-free, visible-light-and triphenylphosphine-mediated intermolecular,
reductive amination between nitroarenes and boronic acids at ambient temperature without …

Comprehensive Summary Transition metal‐catalyzed carbonylation reactions represent a
direct and atom‐economical approach to synthesize carbonyl compounds or their …

Nickel-catalyzed arylcarbamoylation reactions of alkenes of N-(o-haloaryl) acrylamides with
CO and nitroarenes via reductive aminocarbonylation to produce carbamoyl-substituted …