84918-73-0Relevant academic research and scientific papers
Anionic hetero[3,3] and [3,5][ rearrangements of hydroxylamine derivatives accompanied with N-O bond cleavage
Endo,Uchida,Hizatate,Shudo
, p. 1096 - 1105 (2007/10/02)
Aromatic and aliphatic N,O-divinylhydroxylamine systems generated in situ from hydroxylamine derivatives smoothly undergo [3,3] rearrangement. The base-catalyzed formation and rearrangement of enolates or dienolates of N-aryl-O-acylhydroxylamines, N,O-dia
Reaction of Arenediazonium Salts with Nitriles in the Presence of Sodium Carboxylates. A Convenient Synthesis of Unsymmetrical N-Aryl Acyclic Imides
Kikukawa, Kiyoshi,Kono, Kiyoshi,Wada, Fumio,Matsuda, Tsutomu
, p. 3671 - 3672 (2007/10/02)
Reactions of arenediazonium tetrafluoroborates (ArN2BF4), acetonitrile and sodium carboxylates (RCOONa) gave N-acyl acetanilides (ArN(COR)COCH3) in moderate to good yields (Ar=Ph, 2-MeC6H4, 3-MeC6H4, 4-MeC6H4, 2,6-(Me)2C6H3; R=Et, i-Pr, t-Bu, Ph).Acrylonitrile and benzonitrile could be used in the reaction instead of acetonitrile.
