Transition metal-catalysed functionalizations of inert C–H bonds to construct C–C bonds
represent an ideal route in the synthesis of valuable organic molecules. Fine tuning of …

The late‐stage modification of structurally complex peptides bears great potential for drug
discovery, crop protection, and the pharmaceutical industry, among others. Whereas …

Reported in this paper is a step economical method toward the general synthesis of 3-vinyl
chromones via the reactions between readily available o-hydroxyphenyl enaminones and …

A palladium-catalyzed [3+ 2] annulation of substituted aromatic amides with maleimides
providing tricyclic heterocyclic molecules in good to moderate yields through weak carbonyl …

The synthesis of NH-free pyrroles via Pd-catalyzed annulation of enaminones and alkenes
is reported. With the catalysis of Pd (II), the activation of triple C (sp2)–H bonds, including …

A ruthenium (II)‐catalyzed asymmetric intramolecular hydroarylation assisted by a chiral
transient directing group has been developed. A series of 2, 3‐dihydrobenzofurans bearing …

Maleimide and succinimide core moieties are present in various natural products and
pharmaceuticals. In addition, these derivatives can be readily modified into biologically …

The catalytic generation of hypervalent iodine (III) reagents by anodic electrooxidation was
orchestrated towards an unprecedented electrocatalytic C− H oxygenation of weakly …

The development of convenient and mild chalcogenylation reactions for the preparation of
unsymmetrical diaryl sulfides and diaryl selenides has received significant attention in …

Ruthenium complexes are well known as remarkable pre-catalysts for challenging C–H
bond functionalizations. Combining them with other types of chemical reactions in a tandem …