The formation of carbon‐fluorine (C‐F) bonds is an important research field in organic
synthesis because the insertion of a fluorine atom into an organic compound can alter its …

Numerous procedures focus on inserting the fluorine atom into the carbon frameworks of
synthetically useful target molecules using various nucleophilic fluorinating reagents …

In recent years, there has been a dramatic increase in available methods for the installation
of fluorine and fluorine-containing functional groups in organic molecules, 1− 4 and the …

Fluorinated compounds are intriguing for the development of pharmaceuticals,
agrochemicals, and materials, and thus, much effort has been exerted to develop more …

Fluoroalkylation reaction, featuring the transfer of a fluoroalkyl group to a substrate, is a
straightforward and efficient method for the synthesis of organofluorine compounds. In …

Despite increasing pharmaceutical importance, fluorinated arenes remain difficult to
synthesize. Particularly, developing general methods that enables to introduce fluoride on …

Fluorinated organic molecules are increasingly being prepared for a variety of applications,
including pharmaceutical products. However, the supply chain to access the necessary raw …

The presence of aryl C–F bonds in pharmaceuticals and agrochemicals is increasing
rapidly. Incorporation of a fluorine substituent into biologically relevant molecules yields …

The unique and desirable properties of fluorinated compounds in pharmaceutical,
agrochemical, and materials sciences have driven the development of remote fluorination …

Transition metal catalyzed transformations using fluorinating reagents have been developed
extensively for the preparation of synthetically valuable fluorinated targets. This is a topic of …