• image 01
    Volume 1, No.1, 2012
  • image 02
    Volume 1, No.2, 2012
  • image 01
    Volume 1, No.3, 2012
  • image 02
    Volume 2, No.1, 2013
  • image 02
    Volume 2, No.2, 2013
  • image 02
    Volume 2, No.S1, 2013
  • image 02
    Volume 2, No.3, 2013
  • image 02
    Volume 2, No.4, 2013
  • image 02
    Volume 3, No.1, 2014
  • image 02
    Volume 3, No.2, 2014
  • Volume 3, No3
    Volume 3, No.3, 2014
  • Volume 3, No4
    Volume 3, No.4, 2014
  • Volume 4, No1
    Volume 4, No.1, 2015
  • Volume 4, No2
    Volume 4, No.2, 2015
  • Volume 4, No3
    Volume 4, No.3, 2015
  • Volume 4, No4
    Volume 4, No.4, 2015
  • Volume 5, No1
    Volume 5, No.1, 2016
  • Login|Register

  • Home Year Wise CitationsMost Cited Article  (11)

    Total citations for the following article is (11) : Details of Citation

    Synthesis, Molecular Docking Studies and Antibacterial Evaluation of Baylis-Hillman Adducts of Coumarin and Pyran Derivatives using Ionic Liquid under Microwave Irradiation
    A. SUNIL KUMAR, S. KANAKARAJU, B. PRASANNA and G. V. P. CHANDRAMOULI
    Dept. of Chemistry, National Institute of Technology, Warangal-506 004, A.P., India
    Chem Sci Trans., 2013   |   DOI:10.7598/cst2013.415    |    View Abstract | FullText    |   

    This article has been cited by :

    Tania Maria CostaLorena Benathar Ballod TavaresDébora de Oliveira, Fungi as a source of natural coumarins production   
    Applied Microbiology and Biotechnology, August 2016, Volume 100, Issue 15, pp 6571–6584    | View at Journal site     | ISI   
    Amin, Kamelia M et al., Synthesis, characterization and antimicrobial activity of some novel isoindole-1,3-dione derivatives   
    SOURCEDer Pharma Chemica; 2013, Vol. 5 Issue 5, p97    | View at Journal site     | -   
    E. Calcio Gaudino et al., Recent advances and perspectives in the synthesis of bioactive coumarins   
    RSC Adv., 2016,6, 46394-46405    | View at Journal site     | ISI   
    V. A. Sazhnikov et al., 9-diphenylaminoacridines as molecular fluorescent chemosensors for determining polar solvent and amine vapors   
    High Energy Chemistry, November 2013, Volume 47, Issue 6, pp 339–345    | View at Journal site     | ISI   
    Sitanshu Kumar, Kapil Mukesh, Kusum Harjai, and Vasundhara Singh, Synthesis of coumarin based Knoevenagel-Ugi adducts by a sequential one pot five-component reaction and their biological evaluation as anti-bacterial agents   
    Tetrahedron Letters, Volume 60, Issue 1, 3 January 2019, Pages 8-12    | View at Journal site     | ISI   
    Emna Ketata, Haitham Elleuch, et al., Anti-melanogenesis potential of a new series of Morita-Baylis-Hillman adducts in B16F10 melanoma cell line   
    Bioorganic Chemistry, Volume 84, March 2019, Pages 17-23    | View at Journal site     | ISI   
    Prasanta Patra, 4-Chloro-3-formylcoumarin as a multifaceted building block for the development of various bio-active substituted and fused coumarin heterocycles: a brief review   
    New Journal of Chemistry, 2021,45, 14269-14327    | View at Journal site     | ISI   
    Mohamed E.Khalifa, Design, synthesis and molecular docking study of new purine derivatives as Aurora kinase inhibitors   
    Journal of Molecular Structure, Volume 1229, 5 April 2021, 129843    | View at Journal site     | ISI   
    AliGhiami-Shomami, Mona Ashtari-Delivand, Bahram Ghalami-Choobar and Ivo Leito, Computational studies of acidities of some hydroxycoumarins   
    Computational and Theoretical Chemistry, Volume 1190, 15 November 2020, 113008    | View at Journal site     | ISI   
    Joanna Stefaniak,Michał G. Nowak,Marek Wojciechowski,Sławomir Milewski & Andrzej S. Skwarecki, Inhibitors of glucosamine-6-phosphate synthase as potential antimicrobials or antidiabetics – synthesis and properties   
    Journal of Enzyme Inhibition and Medicinal Chemistry, 2022, Volume 37 - Issue 1, Pages 1928-1956    | View at Journal site     | ISI   
    Wafa Mihoubi, Haitham Elleuch, Emna Ketata and Ali Gargouri, Acetate derivative of Morita –Baylis-Hillman adducts (MBH): A powerful antifungal   
    Saudi Journal of Biological Sciences, 2022, 103343    | View at Journal site     | ISI