125593-45-5Relevant academic research and scientific papers
The Chemisty of Acylated Quinone Imine Ketals. Nucleophilic and Organolithium Addition Reactions
Swenton, John S.,Bonke, Brian R.,Clark, William M.,Chen, Chung-Pin,Martin, Kevin V.
, p. 2027 - 2034 (2007/10/02)
Acylated quinone imine ketals are readily available via anodic oxidation of p-methoxybenzanilides and p-methoxyacetanilides.These compounds react with a variety of nucleophiles to give the corresponding substituted 2- and/or 3-substituted-4-methoxyanilide
1,2-Addition of Sulfur Nucleophiles to the N-Acylated Imine Linkage. A Model Study for the Incorporation of Sulfur Nucleophiles during Metabolism of Acylated Aromatic Amines
Clark, William M.,Swenton, John S.
, p. 3969 - 3971 (2007/10/02)
The imine linkage of an acylated quinone imine ketal reacts with ethanethiol to afford an isolable addition product which subsequently rearranges by a facile 1,2-shift to afford an ortho-substituted aromatic amide.
