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

At the advent of cross-coupling chemistry, carbon electrophiles based on halides or
pseudohalides were the only suitable electrophilic coupling partners. Almost two decades …

Copper-catalyzed stereospecific cross-couplings of boronic esters are reported. Boron “ate”
complexes derived from pinacol boronic esters and tert-butyl lithium undergo stereospecific …

Copper-catalyzed oxidative carbon–heteroatom bond formation: a recent update - Chemical
Society Reviews (RSC Publishing) DOI:10.1039/C5CS00882D Royal Society of Chemistry …

This Perspective article outlines some of the recent advancements completed in the
development of (chiral) metal-free and late-transition metal catalysts for the inter-and …

The reaction of various organozinc pivalates with anthranils provides anilines derivatives,
which cyclize under acidic conditions providing condensed quinolines. Using alkenylzinc …

We report a regioselective, nickel-catalyzed syn-1, 2-carboamination of nonconjugated
alkenyl carbonyl compounds with O-benzoyl hydroxylamine (N–O) electrophiles and …

Carbon dioxide (CO2), as a waste of manufacture, is a cheap and abundant C1 source.
Utilization of CO2 for synthesis of carboxylic acids has been developed. Transition-metal …

Transition‐metal‐catalyzed electrophilic amination has been developed into a powerful tool
for C− N bond construction. So far, O‐benzoylhydroxylamines are the most widely used …

The CuH-catalyzed hydroamination of alkenes and alkynes using a silane and an amine
transfer reagent represents a simple strategy to access chiral amine products. We have …