Nitrogen-containing π-excessive aromatic heterocycles, in particular, carbazoles,
indolocarbazoles, benzocarbazoles, and carbolines have been considered the fundamental …

Heterocyclic alkenes represent an important class of reactive feedstock and valuable
synthons for the synthesis of biologically important heterocyclic scaffolds. Although …

A three-component method is described for the preparation of syn-1, 2-disubstituted bridged
bicyclic compounds. The reaction was demonstrated for readily available aromatic and …

A Rh (III)-catalyzed direct cyanation of 2 H-indazoles with N-cyano-N-phenyl-p-
toluenesulfonamide has been realized via a chelation-assisted strategy. The methodology …

Rhodium-catalyzed diverse tandem twofold C–H bond activation reactions of para-olefin-
tethered arenes have been realized, with unsaturated reagents such as internal alkynes …

Transition‐metal‐catalyzed C− H functionalization is one of the fascinating scientific fronts in
organic synthesis for the formation of conjugated arenes and has emerged as a benchmark …

Rhodium-catalyzed directed C–H functionalization of 2-arylindazoles with N-
sulfonylformaldimines has been developed to provide a variety of N-benzylarylsulfonamide …

A new and efficient protocol has been demonstrated for the synthesis of
benzothiadiazinoisoquinoline 6, 6-dioxides and benzothiadiazinoisoindole 5, 5-dioxides in …

A simple and efficient method for the directed amidation of a wide range of 2-arylindazoles
has been established for the first time through a rhodium-catalyzed C–H activation reaction …

An efficient synthesis of benzo [c] phenanthridine alkaloids via a synergistic combination of
C–C bond formation and a cycloaromatization reaction is described. Aryl nitrones react with …