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Rancan, E., Aricò, F., Quartarone, G., Ronchin, L., Tundo, P. and Vavasori A. (2014) Self-Catalyzed Direct Amidation of Ketones: A Sustainable Procedure for Acetaminophen Synthesis. Catalysis Communications, 54, 11-16.
http://dx.doi.org/10.1016/j.catcom.2014.05.007

has been cited by the following article:

• TITLE: The Effective Catalyst (Cobalt Salt/Lewis Acid) for Beckmann Rearrangement of Cycloalkanone Oximes to Lactams under Mild Conditions

  AUTHORS: Masahiro Komeda, Ayana Ozaki, Keita Hayashi, Michinori Sumimoto, Kenji Hori, Tsunemi Sugimoto, Hidetoshi Yamamoto

  KEYWORDS: Beckmann Rearrangement, Cycloalkanone Oximes, Lactam, Cobalt Catalysts, Lewis Acids

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.5 No.2, May 25, 2015

  ABSTRACT: The Beckmann rearrangement of cyclohexanone oxime was achieved by the combined use of cobalt salt and Lewis acids co-catalysts (each 10 mol%). Various combinations of cobalt salts and Lewis acids gave lactams in a satisfactory yield under mild conditions. This method makes it possible to reduce undesirable byproducts.