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J. Dambacher, W. Zhao, A. El-Batta, R. Anness, C. Jiang and M. Bergdahl, “Water is an Efficient Medium for Wittig Reactions Employing Stabilized Ylides and Aldehydes,” Tetrahedron Letters, Vol. 46, No. 26, 2005, pp. 4473-4477. doi:10.1016/j.tetlet.2005.04.105

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.