Hypervalent iodine (III) compounds have found wide application in modern organic
chemistry as environmentally friendly reagents and catalysts. Hypervalent iodine reagents …

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 …

This review summarizes the progress in the fluorination and fluoroalkylation of electron‐rich
systems with diverse fluorine (F) and fluoroalkyl (Rfn) reagents employing hypervalent …

The site-selective modification of amino acids, peptides, and proteins has always been an
intensive topic in organic synthesis, medicinal chemistry, and chemical biology due to the …

A 4-tetrafluoropyridinylthio group was suggested as a new photoredox-active moiety. The
group can be directly installed on difluorostyrenes in a single step by the thiolene click …

Herein we report the design and synthesis of hypervalent trifluoromethylthio-iodine (III)
reagent 1 and the elucidation of its structure by NMR spectroscopy and X-ray …

Hypervalent iodine compounds have found broad application in modern organic chemistry
as reagents and catalysts. Cyclic hypervalent iodine reagents based on the benziodoxole …

Hypervalent iodine compounds are powerful reagents for the development of novel
transformations. As they exhibit low toxicity, high functional group tolerance, and stability in …

Perfluorocarbons, saturated carbon chains in which all the hydrogen atoms are replaced
with fluorine, form a separate phase from both organic and aqueous solutions. Though …

Covalent labeling of proteins in combination with mass spectrometry has been established
as a complementary technique to classical structural methods, such as X-ray, NMR, or …