Research and industrial interest in radical C–H activation/radical cross-coupling chemistry
has continuously grown over the past few decades. These reactions offer fascinating and …

Sulfoximines are widely used as medicines, agricultural chemicals, chiral precursors, and
chiral ligands in asymmetric synthesis, as well as pivotal intermediates for the construction of …

The copper-catalyzed enantioselective intermolecular radical 1, 2-carboamination of
alkenes with readily accessible alkyl halides is an appealing strategy for producing chiral …

Transition‐metal catalyzed enantioconvergent cross‐coupling of tertiary alkyl halides with
ammonia offers a rapid avenue to chiral unnatural α, α‐disubstituted amino acids. However …

Sulfoximine and its congeners are a versatile class of structural motifs widely found in a
plethora of pharmaceutical compounds and crop protection industries due to their …

By exploring a new mode of nickel‐catalyzed cross‐coupling, a method to directly transform
both aromatic and aliphatic aldehydes into either esters or amides has been developed. The …

The electrochemical synthesis of N-aroylsulfoximines features the use of tetra-n-
butylammonium iodide (TBAI) as the medium and a broad substrate scope, thus affording a …

An efficient iron-catalyzed C–N bond formation by hetero-cross-dehydrogenative coupling
(CDC) between sulfoximines and diarylmethanes is described. The reaction shows good …

Sulfoximines are of considerable interest for incorporation into medicinal compounds. A
convenient synthesis of N-protected sulfoximines is achieved, under mild conditions, by …

Two new rhodium‐catalyzed oxidative couplings between sulfoximine derivatives and
alkenes by regioselective C H activation, affording ortho‐olefinated (Heck‐type) products …