142835-76-5Relevant academic research and scientific papers
Acid-catalyzed rearrangement of O-(2-arylphenyl)hydroxylamines to aryldihydroazepinones
Endo, Yasuyuki,Kataoka, Ken-Ichiro,Haga, Naoki,Shudo, Koichi
, p. 3339 - 3342 (1992)
Acid-catalyzed rearrangement of O-(2-arylpheynl) hydroxylamines followed by ring enlargement afford 7-aryl-2, 3-dihydro-1H-azepin-2-ones. 2-Amino-2-phenyl-3, 5-cyclohexadienone, an intermediate of the reaction, was trapped as the N-trifluoroacetamide.
