C− C bond formation is a fundamental transformation in organic synthesis. The development
of new synthetic methodology could be considered as a way of pursuing a novel method for …

A significant number of reactions have appeared in the literature regarding cross
dehydrogenative coupling (CDC) reactions over the years. This review aims to cover the …

A palladium-catalyzed domino process to access unsymmetrical diarylindolylmethanes has
been developed through the annulation of o-alkynylanilines followed by 1, 6-conjugate …

In recent years, the cross-dehydrogenative coupling (CDC) has demonstrated to be a
powerful synthetic tool to form C–C bonds from two C–H bonds. This high atom-economic …

A novel iron-catalyzed dual-oxidative dehydrogenative (DOD) tandem annulation of glycine
derivatives with tetrahydrofurans (THFs) for the synthesis of high value quinoline fused …

The first iron-catalyzed esterification of the primary benzylic C–H bonds with carboxylic acids
using di-tert-butyl peroxide as an oxidant is achieved by novel ionic iron (III) complexes …

An Fe (III)-catalyzed solvent-free cross-dehydrogenative coupling of 3-benzylic indoles and
compounds with acidic methylene groups has been achieved under high-speed ball-milling …

Cross-dehydrogenative-coupling (CDC) between C–H/C–H bonds of indoles and cyclic
ethers/cycloalkanes is made viable through a simple transition-metal-free pathway. With the …

The synthesis and structure of nitrogen-containing heterocycles are fascinating because
these compounds have a great richness of structural, physicochemical, and biological …

A mild procedure for the oxidative C− C cross‐coupling of tertiary anilines with phenols is
described which provides the products generally in high yields and with excellent selectivity …