Differentiating between two highly similar C–H bonds in a given molecule remains a
fundamental challenge in synthetic organic chemistry. Directing group assisted strategies for …

Pd‐catalysis has stood as a pivotal force in synthetic transformations for decades,
maintaining its status as a paramount tool in the realm of C− H bond activation. While …

Organosilicon compounds have shown tremendous potential in drug discovery and their
synthesis stimulates wide interest. Multicomponent cross-coupling of alkenes with silicon …

The directional conversion of methane to ethylene is challenging due to the dissociation of
the C─ H bond and the self‐coupling of methyl intermediates. Herein, a novel W/WO3− x …

Ferrocenyl amines as directing groups for C–H activation have limitations as they are prone
to undergo oxidation, allylic deamination, and β-hydride elimination. The fundamental …

Multicomponent cross-coupling reactions involving alkenes represent a compelling strategy
for accessing three-dimensional molecules, a key pursuit in contemporary medicinal …

Direct arylation of the benzylic C (sp3)–H bond is one of the most straightforward strategies
for the construction of multi-aryl methanes, owing to the extraordinary step and atom …

Transition-metal-catalyzed C–H activation has greatly benefited the synthesis and
development of functional polymer materials, and the construction of multifunctional fused …

The synthetic innovations in generating β-arylethylamines have the potential to propel
advancements in drug discovery, as β-arylethylamines are common structural motifs in …

The development of catalytic methods for the synthesis of enantiopure saturated
heterocycles has been a long-standing challenge in asymmetric catalysis. We describe the …