Hypervalent iodine compounds as environmentally friendly and relatively inexpensive
reagents have properties similar to transition metals. They are employed as alternatives to …

The term “C–H functionalisation” incorporates C–H activation followed by its transformation.
In a single line, this can be defined as the conversion of carbon–hydrogen bonds into …

The interest of scientists in the carbazole core has risen steadily over the last 30 years,
particularly over the last decade given its presence in several active pharmaceutical …

Herein, we present an overview of recent advances in the electrochemical halogenation of
organic compounds. Halogen-containing compounds are essential building blocks for post …

Hypervalent iodine reagents have been extensively employed in various types of oxidative
organic reactions including oxidative coupling/cyclization, bifunctionalization of olefins and …

Reported herein is an environmentally benign electrochemical C− H bond dehydrogenative
amination protocol for the construction of privileged carbazole moiety with broad generality …

We herein disclose the Cp* Co (III)(LX)-catalyzed amidative alkyl migration using 2, 6-
disubstituted phenyl azidoformates. Upon the cobalt–nitrenoid insertion toward the …

Hypervalent iodine chemistry is a rapidly growing area of research with tremendous impact
on synthetic chemistry in the past years. A rich and diverse chemistry is now available for …

The progress in C− N bond construction is significant in synthetic and biological chemistry.
Cross‐dehydrogenative couplings of C− H and N− H motifs serve as a unique class of the …

We report the synthesis of carbazole-based unnatural α-amino acid and non-α-amino acid
derivatives via a Pd (II)-catalyzed bidentate directing group 8-aminoquinoline-aided β-C …