Direct fluoroalkoxylation reactions of (hetero) arenes, carbon‐carbon multiple bonds, and
substitution reactions at Csp3 carbon centers by CF3O, CHF2O, and (CF3) 2CFO groups are …

A solvent free strategy for the mechanochemical synthesis of 3-acylchromones has been
developed via FeCl3-nanocellulose mediated dehydrative coupling of ortho …

An alternative strategy for the mechanochemical defluorinative acylation of ortho‐
hydroxyarylenaminones has been developed to synthesise 3‐acylchromones utilizing CF3 …

Among a wide array of synthetic amides, N-aryl/alkyl amides are an important class of
structural motifs having significant importance in pharmaceutical and agrochemical …

The addition of an amine group to a heteroaromatic system is a challenging synthetic
process, yet it is an essential one in the development of many bioactive molecules. Here, we …

Among the tools available to chemists for drug design of bioactive compounds, the
bioisosteric replacement of atoms or groups of atoms is the cornerstone of modern …

Comprehensive Summary The trifluoromethoxy functional group has received increasing
attention in recent years due to its distinctive properties such as good metabolic stability …

The stoichiometric defluorinative functionalization of ArCF3 is a conceptually appealing
research target. It enables the challenging late-stage functionalization of CF3-containing …

An environmentally friendly, metal-free, and efficient C (sp2)–S coupling reaction protocol
between aniline and low-cost tetraalkylthiuram disulfides was developed to synthesize aryl …

Aromatic amines (AAs), ubiquitous in industrial applications, pose significant environmental
hazards due to their resistance to conventional wastewater treatments. Peracetic acid (PAA) …