Indazole-containing derivatives represent one of the most important heterocycles in drug
molecules. Diversely substituted indazole derivatives bear a variety of functional groups and …

Colorimetric and fluorescent probes based on small organic molecules have become
important tools in modern biology because they provide dynamic information concerning the …

The activation of typically unreactive aromatic C–H bonds by transition-metal catalysis has
been receiving increased attention from the synthetic chemistry community in recent years …

Abstract The first enantioselective Satoh–Miura‐type reaction is reported. A variety of C− N
axially chiral N‐aryloxindoles have been enantioselectively synthesized by an asymmetric …

Transition-metal catalyzed directing group (DG) assisted annulation of inert C–H bonds
leads to the formation of complex molecular frameworks from readily accessible substrates …

Conspectus Conversion of common reactants to diverse products is a key objective of
organic syntheses. Recent developments in transition-metal-catalyzed C–H functionalization …

With different nitrogen‐containing heterocyclic moieties, Indazoles earn one of the places
among the top investigated molecules in medicinal research. Indazole, an important fused …

Pyrazole-containing compounds represent one of the most influential families of N-
heterocycles due to their proven applicability and versatility as synthetic intermediates in …

This review describes recent advances in transition-metal-catalyzed C–H functionalization
reactions of pyrazoles to form new C–C and C–heteroatom bonds on the pyrazole ring. In …

A rhodium catalyzed direct regioselective oxidative annulation by double C–H activation is
described to synthesize highly substituted quinolones from pyridones. The reaction …