The natural occurrence of amides and their unique roles in synthetic materials and
biologically active compounds make amide synthesis one of the most routinely performed …

With the assistance of nickel as catalyst, 2, 2′-bipyridine (bpy) as ligand, and manganese
as reducing metal, the reductive amidation of isocyanates with readily accessible aryl …

A Cu-catalyzed borylative carboxamidation reaction has been developed using vinylarenes
and isocyanates. Alkynes, branched 1, 3-dienes, and bicyclic alkenes were also found to be …

A copper-catalyzed borylative amidation of vinyl arenes with isocyanates and bis
(pinacolato) diboron has been developed. This new protocol, which can be performed on a …

The addition of carbon nucleophiles to isocyanates represents a conceptually flexible and
efficient approach to the preparation of amides. This general synthetic strategy has …

Isocyanates are useful building blocks for the synthesis of amides, although their
widespread use has been limited by their high reactivity, which often results in poor …

An efficient and stereoselective method for the synthesis of (E)-and (Z)-α-silyl-α, β-
unsaturated amides and its synthetic applications are presented herein. The solvent …

Described herein is a distinct protocol for secondary amide formation through a catalyst-free
cross-coupling of isocyanates with triarylboranes. As a practical strategy, this methodology …

Mechanistic studies of a stoichiometric palladium-mediated ExIn (ExIn= extrusion–insertion)
decarboxylative amidation of aromatic carboxylic acids are presented, providing gas-phase …

Nickel-catalyzed reductive amidation of aryl-triazine ethers - Chemical Communications (RSC
Publishing) DOI:10.1039/C9CC08727C Royal Society of Chemistry View PDF VersionPrevious …