Transition-metal-catalyzed C–H activation has developed a contemporary approach to the
omnipresent area of retrosynthetic disconnection. Scientific researchers have been tempted …

Synthetic organic electrosynthesis has grown in the past few decades by achieving many
valuable transformations for synthetic chemists. Although electrocatalysis has been popular …

In the field of C–H bond functionalization chemistry, directed C–H bond activation strategies
are highly appreciated due to the high efficiency and selectivity of such reactions towards a …

C–H activation has emerged as a transformative tool in molecular synthesis, but until
recently oxidative C–H activations have largely involved the use of stoichiometric amounts of …

The indole scaffold will continue to play a vital part in the future of drug discovery and
agrochemical development. Because of this, the necessity for elegant techniques to enable …

Ruthenium-catalysed σ-activation for remote meta -selective C–H functionalisation - Chemical
Society Reviews (RSC Publishing) DOI:10.1039/C7CS00496F Royal Society of Chemistry …

Transition-metal-catalyzed C–H bond functionalization has known a rapid evolution in the
last years, offering modern strategies for reaching high molecular complexity in a step-and …

The elaboration of simple arenes in order to access more complex substitution patterns is a
crucial endeavor for synthetic chemists, given the central role that aromatic rings play in all …

The Catellani reaction is known as a powerful strategy for the expeditious synthesis of highly
substituted arenes and benzo‐fused rings, which are usually difficult to access through …

Visible‐light‐induced ruthenium catalysis has enabled remote C− H alkylations with
excellent levels of position control under exceedingly mild conditions at room temperature …