Oxidative bromination has been serving as a powerful tool for the synthesis of bromo-
containing molecules, as this bromination strategy features environmental friendliness, high …

An efficient regioselective functionalization of 2‐aryl‐heteroarenes and aryl aldehydes via
an azaaryl BF2 complex has been developed. Mechanistically the reaction comprises …

The installation of the C–halogen bond at the ortho position of N-aryl amides and ureas
represents a tool to prepare motifs that are ubiquitous in biologically active compounds. To …

Halogen incorporated arenes and heteroarenes are often used as useful intermediates as
well as target products in organic synthesis. Often, C− H bond halogenation is attempted …

A practical electrophilic bromination procedure for phenols and phenol–ethers was
developed under efficient and very mild reaction conditions. A broad scope of arenes was …

A simple and efficient method has been developed for construction of sulfonylated
quinolines via coupling of haloquinolines and sulfonyl chlorides in water. The present …

A mild, metal-free, and absolutely para-selective bromination of aniline derivatives has been
developed in excellent yields, wherein the organic dye Eosin Y is employed as the bromine …

A metal-and initiator-free direct fluorination of arenes with the assistance of an amide group
is developed. This reaction proceeded under simple aqueous conditions with good …

Electrochemical C–H mono/multi-bromination regulation of N-sulfonylanilines on the cost-
effective CF electrode is described. This reaction proceeds smoothly under mild conditions …

Using LiCl as a chlorine source, the chlorination of 2-aminopyridines or 2-aminodiazines in
the presence of Selectfluor and DMF is established under mild conditions. This method …