All fluorochemicals—including elemental fluorine and nucleophilic, electrophilic, and radical
fluorinating reagents—are prepared from hydrogen fluoride (HF). This highly toxic and …

Introduction Covalent drug discovery has traditionally focused on targeting cysteine, but the
amino acid is often absent in protein binding sites. This review makes the case to move …

A sustainable, mechanochemical procedure for the synthesis of sulfur (VI) fluorides starting
from readily available sulfur (VI) 2-methylimidazoles as stable S (VI) precursors has been …

An increased interest to expand three-dimensional chemical space for the design of new
materials and medicines has created a demand for isosteric replacement groups of …

Flame retardancy is a desirable property of polymer materials, and the molecular design of
novel flame-retardant structures considers three main aspects:(i) the chemical structure …

An effective method was explored for the selective synthesis of sulfonamides and
sulfenamides using sodium sulfinates and amines as starting materials. This method offers …

A modular synthesis of sulfondiimidoyl fluorides—the double aza‐analogues of sulfonyl
fluorides—allowing variation of the carbon and both nitrogen‐substituents is reported. The …

Aryl fluorosulfates of varying complexities have been used in amination reactions in water
using a new Pd oxidative addition complex (OAC‐1) developed specifically to match the …

Aryl fluorosulfates of varying complexities have been used in amination reactions in water
using a new Pd oxidative addition complex (OAC) developed specifically to match the needs …

The development of mild, selective, efficient, and economical chemical transformations is a
foundation of modern synthetic organic chemistry. These chemical processes may be …