Copper-catalyzed C–C bond cleavage and intramolecular cyclization

Chinese scientists have developed a new approach to synthesize acridones viacopper-catalyzed C–C bond cleavage and intramolecular cyclization.

Graphical abstract for C2GC36502BC–C and C–H bond cleavage/activation has become a very important area of research in recent years due to the variety of possible applications.  Presently, the cleavage of C–C bonds generally involves the use of noble metal catalysts such as Rh, Ry, Pd and Pt among others.  However, there are very few examples in the current literature of cheaper metals such as copper or iron being employed in these transformations.

In this work, Wang Zhou and colleagues from Xiangtan University, China, used a copper catalyst and air as the oxidant to synthesize acridones through a C–C bond cleavage and intramolecular cyclization, under neutral conditions.  This reaction provides an alternative strategy for C–C cleavage.

Read the full article for free until the 11th December 2012:

Copper-catalyzed C–C bond cleavage and intramolecular cyclization: an approach toward acridones, Wang Zhou, Youqing Yang, Yong Liu and Guo-Jun Deng, Green Chem., 2012, DOI: 10.1039/C2GC36502B

You may also be interested in these articles – free to access for 2 weeks:

Copper(II) catalysis provides cyclohexanone-derived propargylamines free of solvent or excess starting materials: sole by-product is water, Conor J. Pierce and Catharine H. Larsen, Green Chem., 2012, 14, 2672-2676

An efficient copper-catalyzed formation of highly substituted pyrazoles using molecular oxygen as the oxidant, Mamta Suri, Thierry Jousseaume, Julia J. Neumann and Frank Glorius, Green Chem., 2012, 14, 2193-2196

A highly efficient Cu-catalyst system for N-arylation of azoles in water, Deping Wang, Fuxing Zhang, Daizhi Kuang, Jiangxi Yu and Junhua Li, Green Chem., 2012, 14, 1268-1271

Microwave-assisted solvent- and ligand-free copper-catalysed cross-coupling between halopyridines and nitrogen nucleophiles, Zhen-Jiang Liu, Jean-Pierre Vors, Ernst R. F. Gesing and Carsten Bolm, Green Chem., 2011, 13, 42-45

Stay up-to-date with the latest news and content in Green Chemistry by registering for our free table of contents alerts.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)