M. C. Dutta, K. Chanda, E. Karim and J. N. Vishwa- karma, “A Facile Route to Enaminones: Synthesis of 3-Alkyl/aralkyl/arylamino-1-arylprop-2-en-1-ones,”In-dian Journal of Chemistry, Vol. 36, No. 11, 2004, pp. 2471-2472.

has been cited by the following article:

• TITLE: Synthesis of Novel Bis-enaminones by KHSO4-assisted Facile Michael Addition-elimination Reaction of 3-(dimethylamino)-1-phenylprop-2-en-1-ones with Diamines in Water

  AUTHORS: Asem Satyapati Devi, Philippe Helissey, Jai Narain Vishwakarma

  KEYWORDS: Enaminone, Bis-enaminone, Formylated Acetophenone, Michael Addition-Elimination, Formylation, Dimethylformamide-dimethylacetal

  JOURNAL NAME: Green and Sustainable Chemistry, Vol.1 No.2, April 13, 2011

  ABSTRACT: 3-(Dimethylamino)-1-phenylprop-2-en-1-ones (formylated acetophenones) 1 reacted with aliphatic diamines in water assisted by KHSO4 to give bis-enaminones 2a-h in good yields. Compound 1 also reacted with o-phenylenediamine under similar conditions to produce bis-enaminones 3 instead of benzodiazepines 4 in excellent yields.