C–H activation has surfaced as an increasingly powerful tool for molecular sciences, with
notable applications to material sciences, crop protection, drug discovery, and …

In the field of C–H bond functionalization chemistry, directed C–H bond activation strategies
are highly appreciated due to the high efficiency and selectivity of such reactions towards a …

Electrochemical oxidation represents an environmentally friendly solution to conventional
methods that require caustic stoichiometric chemical oxidants. However, C–H …

Transformations of aromatic compounds into the corresponding amines, amides, and imides
through carbon–hydrogen (C–H) bond functionalization represent one of the most step-and …

Transition metal-catalyzed direct functionalization of C–H bonds has recently emerged as a
powerful strategy for the construction of carbon–carbon and carbon–heteroatom bonds …

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 …

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 …

Herein, we report a photoinduced sulfoximine-to-copper charge-transfer-enabled generation
of sulfoximinyl radicals directly from NH-sulfoximines for C–H sulfoximination of arenes via …

The direct amination of C–H bonds with ammonia is a challenge in synthetic chemistry.
Herein, we present a copper-mediated approach that enables a chelation-assisted aromatic …

Nickel-Catalyzed Direct Thiolation of C(sp3)–H Bonds in Aliphatic Amides | Organic Letters
ACS ACS Publications C&EN CAS Find my institution Log In Organic Letters ACS Publications …