Alcohols are abundant and attractive feedstock molecules for organic synthesis. Many
methods for their functionalization require them to first be converted into a more activated …

A single-atom catalyst with generally regarded inert Zn–N4 motifs derived from ZIF-8 is
unexpectedly efficient for the activation of alcohols, enabling alcohol-mediated alkylation …

Cross‐coupling of nitriles and alcohols offers an environmentally friendly and atom‐
economical method for the synthesis of various valuable compounds. These compounds …

A highly efficient, in situ formed CuCl2/TMEDA catalytic system (TMEDA= N, N, N′, N′-
tetramethylethylene-diamine) for the cross-coupling reaction of aryl acetonitriles with benzyl …

Despite the limited success of copper-catalyzed alkylations,(NNS) CuCl proved to be an
effective catalyst for the sp3 C–H alkylation of fluorene with alcohols. Various primary …

The utilization of earth-abundant, cheap, and nontoxic transition metals in important catalytic
transformations is essential for sustainable development, and iron has gained significant …

The nickel phosphides have garnered increasing attention as an excellent catalytic site in
the fields of electrocatalysis and hydrotreating, but their application in organic synthesis …

The utilization of economical and environmentally benign transition metals in crucial
catalytic processes is pivotal for sustainable advancement in synthetic organic chemistry …

Herein, we have reported a new series of NNS‐donor ligands coordinated Ni (II) complexes
and utilized them as catalytic activator to synthesize N‐alkylated amines and 1, 2 …

The borrowing hydrogenation (BH) and acceptorless dehydrogenative coupling (ADC)
methods emerged as sustainable tools for forging carbon–carbon bonds at remarkably …