Metal-catalyzed regiodivergent reactions allow control over regioselectivity in the synthesis
of a wide range of organic products. Starting from the same material, it is possible to prepare …

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

Methods that can simultaneously install multiple different functional groups to heteroarenes
via C− H functionalizations are valuable for complex molecule synthesis, which, however …

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 …

The excellent functional group tolerance of the Suzuki–Miyaura cross-coupling reactions
has been decisive for their success in the pharmaceutical industry. Highly diversified …

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 new class of bidentate ligands was prepared by a modular approach involving Rh-
catalyzed C–H annulation reactions. The resulting conformationally constrained ligands …

Abstract 6π electrocyclization has attracted interest in organic synthesis because of its high
stereospecificity and atom economy in the construction of versatile 5–7‐membered cycles …

A novel route has been reported for C–H hydroxylation of benzyl compounds directed by a
3, 4, 5-tribromopyrazole auxiliary via boronation/oxidation using BBr3 and NaBO3· 4H2O …