B. H. Lipshutz and M. C. Morey, “An Approach to the Cyclopeptide Alkaloids (Phencyclopeptines) via Heterocyclic Diamide/Dipeptide Equivalents. Preparation and N-Alkylation Studies of 2,4(5)-Disubstituted Imidazoles,” The Journal of Organic Chemistry, Vol. 48 , No. 21, 1983, pp. 3745-3750. http://dx.doi.org/10.1021/jo00169a027

has been cited by the following article:

• TITLE: Solvent Free One-Pot Synthesis of 1,2,4,5-Tetrasubstituted Imidazoles Catalyzed by Secondary Amine Based Ionic Liquid and Defective Keggin Heteropoly Acid

  AUTHORS: Pranab Jyoti Das, Jupitara Das, Munni Ghosh, Sabera Sultana

  KEYWORDS: Ionic Liquids; Keggin Heteropolyacid; Microwave; Tetrasubstituted Imidazole; Solvent Free Synthesis; Multicomponent Reaction

  JOURNAL NAME: Green and Sustainable Chemistry, Vol.3 No.4A, November 22, 2013

  ABSTRACT: Secondary amine based ionic liquid and defective Keggin type heteropoly acid (HPA) are separately used for efficient one-pot four-component synthesis of 1,2,4,5-tetrasubstituted imidazoles assisted by microwave (MW). Eco-friendly solvent free procedure, short reaction time, high yield of products and reusability of catalysts are important features of the synthesis. A comparative study on the efficiency of the two catalysts is reported. This work further demonstrates the alternate use of urea, instead of often used ammonium acetate, as source of nitrogen.