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Makki, M.S.T., Bakhotmah, D.A. and Abdel-Rahman, R.M. (2012) Highly Efficient Synthesis of Novel Fluorine Bearing Quinoline-4-Carboxylic Acid and the Related Compounds as Amylolytic Agents. International Journal of Organic Chemistry, 2, 49-55.

has been cited by the following article:

• TITLE: Synthesis of Some New Fluorine Substituted Thiobarbituricacid Derivatives as Anti HIV1 and Cyclin-Dependent Kinase 2 (CDK2) for Celltumer Division-Part II

  AUTHORS: Abdulrahman S. Al-Harbi, Reda M. Abdel-Rahman, Abdullah M. Asiri

  KEYWORDS: Fluorinated Thiobarbituric, Heterobicyclic, Potential Inhibitors

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.4 No.2, June 25, 2014

  ABSTRACT: In search for new potential inhibitors some new fluorine substituted thiobarbituric acid derivatives (2-4, 7, 8) and their fused/isolated heterobicyclic nitrogen systems (5, 6, 9, 10, 11, 12) have been synthesized from heterocyclization of fluorinated 1,3-diketoamine (1) with CS2 followed by ring closure reactions with primary nitrogen reagents. Structures of the targets have been established from elemental analysis and spectral data. Some synthesized systems have been evaluated as anti-HIV-1 and of cyclin-dependent kinase 2 (CDK2) for cell tumor division.