Wednesday, March 28, 2012

Ligand-free copper-catalyzed coupling of nitroarenes with arylboronic acids


The first example of copper-catalyzed coupling of nitroarenes with arylboronic acids was developed, providing diaryl ethers in moderate to excellent yields. The efficiency of this reaction was demonstrated by compatibility with a wide range of groups. Moreover, the rigorous exclusion of air/moisture is not required in these transformations. Thus, the method represents a simple and facile procedure to access diaryl ethers. Preliminary mechanistic experiments using deuterium labeling showed that the oxygen atom was derived from water.


Graphical abstract: Ligand-free copper-catalyzed coupling of nitroarenes with arylboronic acids

Green Chem., 2012, 14, 912-916

Copper-catalyzed highly efficient aerobic oxidative synthesis of imines from alcohols and amines

Graphical abstract: Copper-catalyzed highly efficient aerobic oxidative synthesis of imines from alcohols and amines

A highly efficient and green tandem imine synthesis from alcohol and amine with molecular oxygen as oxidant was achieved by using a remarkable low catalyst-loading, with a commercially available and environmentally benign copper catalyst.

Wednesday, March 14, 2012

N-Heterocyclic carbene chemistry of iron: fundamentals and applications

Graphical abstract: N-Heterocyclic carbene chemistry of iron: fundamentals and applications

Michael J. Ingleson and Richard A. Layfield, Chem. Commun., 2012, 48, 3579-3589

Regioselective solvent-dependent benzannulation of conjugated enynes

Graphical abstract: Regioselective solvent-dependent benzannulation of conjugated enynes

Florian Pünner and Gerhard Hilt, Chem. Commun., 2012, 48, 3617-3619

Wednesday, March 7, 2012