A. Debache, M. Amimour, A. Belfaitah, S. Rhouati and B. Carboni, “A One-Pot Biginelli Synthesis of 3,4-Dihydropyrimidin-2-(1)-Ones/Thiones Catalyzed by Triphenylphosphine as Lewis Base,” Tetrahedron Letters, Vol. 49, No. 42, 2008, pp. 6119-6121.
http://dx.doi.org/10.1016/j.tetlet.2008.08.016

has been cited by the following article:

• TITLE: Phase Transfer Catalysis Improved Synthesis of 3,4-Dihydropyrimidinones

  AUTHORS: Hela Slimi, Khemaïs Saïd, Younes Moussaoui, Ridha Ben Salem

  KEYWORDS: Multicomponent Reaction; Biginelli Reaction; 3, 4-Dihydropyrimidinones; Phase-Transfer Catalysis; Quaternary Ammonium Salts

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.3 No.3A, November 28, 2013

  ABSTRACT: Various 3,4-dihydropyrimidinones can be prepared via Biginelli reaction in aqueous media by using quaternary ammonium salts of different alkyl groups (C4 and C8) and anions (Cl-and Br-) as catalysts. The use of quaternary ammonium salts along with longer alkyl chains increases the yield of the Biginelli reaction; however, bromide ammonium salts are less active than the chloride ones.