Achieving selective C− H activation at a single and strategic site in the presence of multiple
C− H bonds can provide a powerful and generally useful retrosynthetic disconnection. In this …

Sequential, domino and tandem reactions could be defined as a sequence of synthetic
transformations that occur one after the other, in the same reaction flask. This Review …

Four cobalt‐catalyzed oxidative annulation reactions of nitrogen‐containing arenes with
alkynes proceeds by C− H activation, thus leading to biologically useful quaternary …

Organic transformations catalyzed by cyclopentadienyl complexes of Group 9 metals (cobalt,
rhodium and iridium) are the key steps of the total synthesis of various natural products …

A green atom‐economical method for the synthesis of highly functionalized 1‐amino and 1‐
carbon substituted isoquinolines from the reaction of N′‐hydroxybenzimidamides and aryl …

By virtue of a synergistically dual-directing-group (the O–NHAc part and the hydroxyl group)-
assisted strategy, the efficient and practical Rh (III)-catalyzed regioselective redox-neutral C …

Abstract Die selektive C‐H‐Aktivierung an einer einzigen und strategisch wichtigen Position
in Gegenwart von zahlreichen weiteren C‐H‐Bindungen kann einen leistungsfähigen und …

Transition-metal-catalyzed C―H functionalization reactions, assisted by directing groups
(DGs), have become some of the most powerful strategies to form C―C and C―X (X= O, N …

The C− H bond activation reactions catalyzed by a transition metal have always been a topic
of intense research. Although the incorporation or removal of a directing group plays an …

An efficient, mild and redox‐neutral iridium (III)‐catalyzed C− H annulation of N‐
phenoxyacetamides for the regioselective synthesis of benzofurans has been developed by …