The present review is devoted to summarizing the recent advances (2015–2017) in the field
of metal-catalysed group-directed C–H functionalisation. In order to clearly showcase the …

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 …

The objective of this report is to investigate the inhibition of cationic gemini-surfactants
based on waste cooking, as a green source of inhibitors against acidic corrosion of N80 …

Sulfoximines with stereogenic sulfur atoms are attractive structural motifs in drug discovery.
A direct catalytic enantioselective method for the synthesis of sulfur‐chiral 1, 2 …

Chiral sulfoximines with stereogenic sulfur atoms are promising motifs in drug discovery. We
report an efficient method to access chiral sulfoximines through a C− H functionalization …

Herein we report a highly para-selective C–H olefination of aniline derivatives by a Pd/S, O-
ligand-based catalyst. The reaction proceeds under mild reaction conditions with high …

A mild visible‐light‐induced Pd‐catalyzed intramolecular C− H arylation of amides is
reported. The method operates by cleavage of a C (sp2)− O bond, leading to hybrid aryl Pd …

Nickela‐electrooxidative C− H alkoxylations with challenging secondary alcohols were
accomplished in a fully dehydrogenative fashion, thereby avoiding stoichiometric chemical …

Rhodium‐electrocatalyzed arene C− H oxygenation by weakly O‐coordinating amides and
ketones have been established by bimetallic electrocatalysis. Likewise, diverse …

The direct Pd-catalyzed ortho C–H hydroxylation of benzaldehydes was achieved using 4-
chloroanthranilic acid as the transient directing group, 1-fluoro-2, 4, 6-trimethylpyridnium …