This Review examines recent developments in late transition metal-catalyzed
hydroamination and-amidation reactions. A hydroamination is a reaction in which an N− H …

Sequential reactions, through the incorporation of several distinct transformations into one
single sequence, are one of the most powerful synthetic tools in modern organic chemistry …

Providing comprehensive insight into the use of copper in cross-coupling reactions, Copper-
Mediated Cross-Coupling Reactions provides a complete up-to-date collection of the …

Copper-catalyzed cross-coupling reactions which lead to the formation of C–N, C–O, C–S
and C–C bonds have been recognized as one of the most useful strategies in synthetic …

CuI/4-hydroxy-l-proline-catalyzed coupling of aryl bromides and N-Boc hydrazine takes
place in DMSO at 80° C to give N-aryl hydrazides. When aryl iodides are employed, this …

The reaction of 2-alkynyl-1-methylene azide aromatics 1 with iodine gives 1, 3-disubstituted
4-iodoisoquinolines 3, and the treatment of 1 with a gold–silver combined catalyst affords …

Seven membered heterocyclic Azepine and its derivatives have great pharmacological and
therapeutic implications. In this review, the literature of the last fifty years has been exploited …

“I” did it: A sequential intramolecular amination/N‐demethylation/amidation of internal
acetylenes in the presence of a catalytic amount of Pd (OAc) 2 and nBu 4 NI afforded indolo …

A redox-neutral bimetallic Rh (III)/Ag (I) relay catalysis allowed the efficient construction of 3-
alkylidene isoindolinones and 3-alkylidene isobenzofuranones. The Rh (III) catalyst was …

Going green! The rhodium (III)‐catalyzed annulation of aryl ketone O‐methyl oximes with
isocyanates for the synthesis of 3‐methyleneisoindolin‐1‐ones is reported (see scheme) …