Journal of the American Chemical Society

Quinone Imides. V. Aluminum Chloride-catalyzed Arylations of p-Quinone Dibenzenesulfonimides

R Adams, KR Eilar

Index: Adams; Eilar Journal of the American Chemical Society, 1951 , vol. 73, p. 1149,1151

Full Text: HTML

Citation Number: 9

Abstract

Aromatic hydrocarbons, phenols and phenolic ethers in the presence of aluminum chloride react with p-quinone dibenzenrsulfonimides to give 2-aryl-p- phenylenedibenzenesulfonamides in yields of 26 to 67y0. In the addition of bydrocarbons, it is essential that the quinone diimide be added to the aluminum chloride in the hydrocarbon; addition of the aluminum chloride to the hydrocarbon solution of the quinone diimide ...

Related Articles:

Hydrocarbon oxidation by Bis-μ-Oxo manganese dimers: electron transfer, hydride transfer, and hydrogen atom transfer mechanisms

[Larsen, Anna S.; Wang, Kun; Lockwood, Mark A.; Rice, Gordon L.; Won, Tae-Jin; Lovell, Scott; Sadilek, Martin; Turecek, Frantisek; Mayer, James M. Journal of the American Chemical Society, 2002 , vol. 124, # 34 p. 10112 - 10123]

More Articles...