Synthetically and biologically interesting N-acyl quinone imine ketals and N-acyl quinol imine ethers from anodic oxidation of anilides

CP Chen, CT Chou, JS Swenton

Index: Chen, Chung-Pin; Chou, Chun-Tzer; Swenton, John S. Journal of the American Chemical Society, 1987 , vol. 109, # 3 p. 946 - 948

Full Text: HTML

Citation Number: 18

Abstract

The electrochemistry of aromatic amines has been extensively studied; l however, less is known about the electrochemical oxidation of the corresponding Several types of reactions have been reported, but most involved poor yields and/or material balances and no synthetic use has been made of this chemistry. Thus, the anodic oxidation of simple anilides in acetonitrile/pyridine gives pyridination prod~ cts,~~~~~~~ while amide derivatives of p- ...

Related Articles:

Microwave-assisted demethylation of methyl aryl ethers using an ionic liquid

[Park, Jiyeon; Chae, Junghyun Synlett, 2010 , # 11 p. 1651 - 1656]

Pd nanoparticles immobilized on PNIPAM–halloysite: highly active and reusable catalyst for Suzuki–Miyaura coupling reactions in water

[Hong, Myeng Chan; Ahn, Hyunseok; Choi, Myung Chan; Lee, Yongwoo; Kim, Jongsik; Rhee, Hakjune Applied Organometallic Chemistry, 2014 , vol. 28, # 3 p. 156 - 161]

Efficient Cleavage of Alkyl Aryl Ethers Using an Ionic Liquid under Microwave Irradiation

[Park, Se Kyung; Battsengel, Oyunsaikhan; Chae, Junghyun Bulletin of the Korean Chemical Society, 2013 , vol. 34, # 1 p. 174 - 178]

Efficient Cleavage of Alkyl Aryl Ethers Using an Ionic Liquid under Microwave Irradiation

[Park, Se Kyung; Battsengel, Oyunsaikhan; Chae, Junghyun Bulletin of the Korean Chemical Society, 2013 , vol. 34, # 1 p. 174 - 178]

A Highly Active and General Catalyst for the Stille Coupling Reaction of Unreactive Aryl, Heteroaryl, and Vinyl Chlorides under Mild Conditions

[Lee, Dong-Hwan; Qian, Yingjie; Park, Ji-Hoon; Lee, Jong-Suk; Shim, Sang-Eun; Jin, Myung-Jong Advanced Synthesis and Catalysis, 2013 , vol. 355, # 9 p. 1729 - 1735]

More Articles...