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Patil, A.D., Kumar, N.V., Kokke, W.C., Bean, M.F., Freyer, A.J., Debrosse, C., Mai, S., Trunch, A., Faulkner, D.J., Carte, B., Been, A.L., Herzberg, R.P., Johnson, R.K., Wastly, J.W. and Ports, B.C.M. (1995) Novel Alkaloids from the Sponge Batzella sp.: Inhibitors of HIV gp120-Human CD4 Binding. Journal of Organic Chemistry, 60, 1182.
https://doi.org/10.1021/jo00110a021

has been cited by the following article:

• TITLE: Synthesis of Some Hexahydroquinazolinones Using K3AlF6(Al2O3/KF) as an Efficient Catalyst in Some Hexahydroquinazolinone Derivatives

  AUTHORS: Masoumeh Mehrabi, Asadollah Farhadi, Alireza Kiassat

  KEYWORDS: 4-Aryl-1, 3, 4, 6, 7, 8-Hexahydroquinazolin-2, 5(1H, 6H)-Diones (HHQs), K3AlF6(Al2O3/KF), 1, 3-Cylohexadione, Acetonitrile

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.7 No.3, August 9, 2017

  ABSTRACT: A protocol for the synthesis of some 4-Aryl-1,3,4,6,7,8-hexahydroquinazolin-2,5(1H,6H)-diones (HHQs) was developed by means of a three-component condensation reaction of an aromatic aldehyde, 1,3-cylohexadione and urea in the presence of K3AlF6 (Al2O3/KF) as catalyst. This reaction is carried out under different conditions including 1) solvent free; 2) reflux in acetonitrile; 3) reflux in ethanol; 4) reflux in chloroform; and 5) reflux in water. In all conditions, the desired products are obtained in high yields after relatively short reaction times. Nevertheless, the reactions proceed faster and in higher yields when they were carried out in acetonitrile. This adopted protocol for some Biginelli-type products has offered the advantages of reusability of the catalyst, high yields and ease of separation of pure products. Furthermore, the catalyst is easily prepared, stabilized and efficiently used under reaction conditions.