Electrochemistry utilizes electrons as a potent, controllable, and traceless alternative to
chemical oxidants or reductants, and typically offers a more sustainable option for achieving …

The current status of homogeneous iron catalysis in organic chemistry is contemplated, as
are the reasons why this particular research area only recently starts challenging the …

As alcohols are ubiquitous throughout chemical science, this functional group represents a
highly attractive starting material for forging new C–C bonds. Here, we demonstrate that the …

Nickel-catalyzed reductive cross-electrophile coupling reactions are becoming increasingly
important in organic synthesis, but application at scale is limited by three interconnected …

The present review “Iron Catalysis in Organic Synthesis” covers the literature until the end of
June 2014 and represents a comprehensive update of a previous article published by Bolm …

Reductive cross‐electrophile coupling reactions have recently been developed to a versatile
and sustainable synthetic tool for selective C C bond formation. The employment of cheap …

A critical overview of the catalytic joining of two different electrophiles, cross-electrophile
coupling (XEC), is presented with an emphasis on the central challenge of cross-selectivity …

The direct cross-coupling of two different electrophiles, such as an aryl halide with an alkyl
halide, offers many advantages over conventional cross-coupling methods that require a …

The Ni-catalyzed reductive coupling of alkyl/aryl with other electrophiles has evolved to be
an important protocol for the construction of C–C bonds. This chapter first emphasizes the …

Alkyl chlorides and aryl chlorides are among the most abundant and stable carbon
electrophiles. Although their coupling with carbon nucleophiles is well developed, the cross …