The hydroarylation of alkynes, alkenes, and allenes is a cost-effective and efficient way to
incorporate unsaturated moieties into aromatic substrates. This review focuses on gold …

The pyrrolo [1, 2-a] indole unit is a privileged heterocycle found in numerous natural
products and has been shown to exhibit diverse pharmacological properties. Thus, recent …

Ru (II)-catalyzed enantioselective C–H activation/hydroarylation has been developed for the
first time, allowing for highly enantioselective synthesis of indoline derivatives via catalytic C …

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

Until now, the selective (hetero) aryl C–H alkylation without the assistance of directing
groups or preinstallation of functionalities still remains a highly challenging goal. Herein, by …

C–H oxygenations of synthetically meaningful sulfoximine benzamides were accomplished
by a versatile ruthenium catalysis regime. The ruthenium (II) catalyst was characterized by …

The transition-metal-catalyzed intramolecular hydroarylation of alkenes has been
recognized as a straightforward approach for the construction of 3, 3-disubstituted 2, 3 …

Metal-catalyzed hydroarylation reactions are always powerful tools in organic synthesis
since they can form C–C or C-heteroatom bonds in an atom and step economic manner …

Efficient construction of quaternary carbon centers represents one of the most challenging
goals in organic synthesis, and it has drawn tremendous research interest from organic …

One-pot synthesis of oxygen-containing heterocycles has been achieved through
alkylation/acylation of 2-hydroxyphenyl-substituted para-quinone methides followed by an …