-transparent.png){kind=logo}
Palladium-catalyzed decarboxylative ortho-amidation of O-methyl ketoximes with oxamic acids. 2019
CAS Key Laboratory of Soft Matter Chemistry, Hefei National Laboratory for Physical Sciences at Microscale and Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China. gwang@ustc.edu.cn.
The first palladium-catalyzed ortho-amidation of ketoximes has been developed with readily available, easy to handle and environment-friendly N,N-disubstituted oxamic acids as the amidation sources. When N-monosubstituted oxamic acids are used as the substrates, the formed ortho-amidated ketoximes undergo further intramolecular cyclization to provide 3-methyleneisoindolinones.
| UI | MeSH Term | Description | Entries |
|---|
Related Publications
Kun Jing, and
Peng-Cheng Cui, and
Guan-Wu Wang
January 2013,
Chemical communications (Cambridge, England),
Kun Jing, and
Peng-Cheng Cui, and
Guan-Wu Wang
October 2015,
Organic letters,
Kun Jing, and
Peng-Cheng Cui, and
Guan-Wu Wang
March 2022,
Molecules (Basel, Switzerland),
Kun Jing, and
Peng-Cheng Cui, and
Guan-Wu Wang
February 2013,
Chemical communications (Cambridge, England),
Kun Jing, and
Peng-Cheng Cui, and
Guan-Wu Wang
July 2017,
ACS omega,
Kun Jing, and
Peng-Cheng Cui, and
Guan-Wu Wang
October 2013,
The Journal of organic chemistry,
Kun Jing, and
Peng-Cheng Cui, and
Guan-Wu Wang
December 2017,
The Journal of organic chemistry,
Kun Jing, and
Peng-Cheng Cui, and
Guan-Wu Wang
June 2013,
Organic letters,
Kun Jing, and
Peng-Cheng Cui, and
Guan-Wu Wang
April 2018,
The Journal of organic chemistry,
Kun Jing, and
Peng-Cheng Cui, and
Guan-Wu Wang
September 2010,
Journal of the American Chemical Society,
