Transition metal-catalyzed direct functionalization of C–H bonds is one of the key emerging
strategies that is currently attracting tremendous attention with the aim to provide alternative …

The catalytic functionalization of unreactive C− H bonds has recently brought a revolution in
synthetic methodologies for the production of pharmaceuticals and natural products and for …

To improve the atom-and step-economy of organic syntheses, researchers would like to
capitalize upon the chemistry of otherwise inert carbon–hydrogen (C–H) bonds. During the …

This review is focused on the analysis of current data on new methods of alkenylation of
arenes and heteroarenes with alkynes by transition metal catalyzed reactions …

The transition metal-catalyzed C–H functionalization with hydroxylamine derivatives serving
as both reactants and internal oxidants has attracted a lot of interest. These reactions …

The use of directing groups has proven to be a successful strategy to enhance reactivity and
control selectivity in C–H functionalization reactions. In the past decade, a multitude of new …

This review covers some unique diazo compounds, the coupling partners to access various
versatile functionalized nitrogen heterocycles, such as indoles, indolines, isoquinolines …

Transition-metal-catalyzed C–H activation followed by oxidative cyclization with unsaturated
coupling partners has been a valuable synthetic tool for the multiring molecular scaffolds …

Significant progress has been accomplished in direct olefinations through twofold C–H bond
functionalization of arenes and heteroarenes employing readily accessible, selective and …

The synthesis of isoquinolines by site‐selective C H activation of O‐acyl oximes with a Cp*
CoIII catalyst is described. In the presence of this catalyst, the C H activation of various …