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

The cation− π interaction is an attractive noncovalent interaction between a cation and a π
system. Due to the stronger interaction energy than those of the other π interactions, such as …

Chromone and flavone are both central backbones of natural products and clinical
medicines. Synthesis of diversely functionalized chromones and flavones constitutes …

Nitration of aromatic compounds represents a powerful and widely used transformation that
allows introducing nitro group into aromatic systems. New synthetic strategies for aromatic …

Nitroaromatic compounds play an important role in organic synthesis, medicinal chemistry
and chemical industry. Among the recently reported synthetic methods to access …

Inhibition of the RNA-binding protein LIN28 and disruption of the protein–RNA interaction of
LIN28–let-7 with small molecules holds great potential to develop new anticancer …

An additive-free, visible light-driven annulation between N-aryl amino acids and maleimide
to form tetrahydroquinolines (THQs) is disclosed. Photochemical activation of an electron …

An efficient C3–H functionalization of indazole has been demonstrated. Notably, this method
involves chelation-free radical C–H nitration on 2H-indazole. The radical mechanism was …

An efficient and cost-effective copper-mediated aerobic oxidative C–H iodination and
nitration of indoles via double C–H functionalization is reported. The domino process …

A mild and selective radical nitration/nitrosation of indoles with NaNO2 using K2S2O8 as
oxidant is developed. Free (NH)‐indoles and N‐methyl indoles furnished 3‐nitro‐and 3 …