The annulative π‐extension (APEX) reaction has the potential to have a tremendous impact
on the fields of materials science and bioimaging, as well as on the pharmaceutical …

Nitrogen-containing π-excessive aromatic heterocycles, in particular, carbazoles,
indolocarbazoles, benzocarbazoles, and carbolines have been considered the fundamental …

Annulative π-extension (APEX) has emerged as a powerful and efficient synthetic method
for the construction of polycyclic aromatic hydrocarbons, nanographenes, and π-extended …

Carbon–carbon/carbon–heteroatom bond formation via oxidative transformations is a
heavily explored topic at the frontier of chemistry. Potassium persulfate (K2S2O8) has …

The activation of typically unreactive aromatic C–H bonds by transition-metal catalysis has
been receiving increased attention from the synthetic chemistry community in recent years …

Carbazoles are privileged nitrogen heterocycles that are present in a wide range of natural
products, pharmaceuticals, and functional materials. Due to their wide application, various …

The direct introduction of alkenyl groups into the indole framework avoiding its preliminary
functionalization can be carried out using different synthetic strategies. Transition‐metal …

The catalytic conversion of lignin into heterocyclic aromatic compounds holds significant
promise not only for expanding lignin's utility in pharmaceutical synthesis but also for …

Considering their unique electronic properties and diverse biological activities,
regioselective access to fused aromatic compounds is significantly important in the field of …

The synthesis of functionalized carbazoles as privileged nitrogen heterocycles has emerged
as a central topic in drug discovery and material science. We herein disclose the rhodium …