As two coexisting and fast-growing research fields in modern synthetic chemistry, the
merging of organocatalysis and C–H bond functionalization is well foreseeable, and the joint …

The direct functionalization of C H bonds in organic compounds has recently emerged as a
powerful and ideal method for the formation of carbon–carbon and carbon–heteroatom …

Functionalizing traditionally inert carbon–hydrogen bonds represents a powerful
transformation in organic synthesis, providing new entries to valuable structural motifs and …

In chemistry, a nucleophile is a molecule or ion with a lone pair of electrons. It donates both
bonding electrons to its reaction partner (the electrophile) when forming a chemical bond. 1 …

Transition‐metal‐catalyzed C H activation has recently emerged as a powerful tool for the
functionalization of organic molecules. While many efforts have focused on the …

Die direkte Funktionalisierung von C‐H‐Bindungen in organischen Molekülen hat sich in
jüngster Zeit zu einer wirksamen und idealen Methode entwickelt, mit der Kohlenstoff …

Sulfoxides are capable of forming stable complexes with transition metals and there have
been many comprehensive studies into their binding properties. However, the use of …

Direct selective palladium catalyzed C–H functionalization has become a highly attractive
strategy in organic synthesis and represents a highly desirable goal. Compared with cross …

Sulfoxides are classical functional groups for directing the stoichiometric metalation and
functionalization of C− H bonds. In recent times, sulfoxides have been given a new lease on …

Transition-metal-catalyzed coupling reactions have become a versatile tool for chemical
bond formation. From the variation of the coupling partners, coupling reactions can be …