Dnyaneshwar Subhedar

Employment

Employment history is unavailable.

Education

• Institute of Chemical Technology Postdoctral Fellow
  2017 - Present
• Dr. babasaheb Ambedkar marathwada university Ph. D
  2012 - 2016

Projects & Funding

Projects & funding information is unavailable.

Publications (15)

• Facile and solvent-free domino synthesis of new quinolidinyl-2,4-thiazolidinones: Antifungal activity and molecular docking
  Mini-Reviews in Medicinal Chemistry 2018 DOI: 10.2174/1389557516666161226161152
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• Quinolidene based monocarbonyl curcumin analogues as promising antimycobacterial agents: Synthesis and molecular docking study
  Bioorganic and Medicinal Chemistry Letters 2017 DOI: 10.1016/j.bmcl.2017.01.004
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• Quinolidene-rhodanine conjugates: Facile synthesis and biological evaluation
  European Journal of Medicinal Chemistry 2017 DOI: 10.1016/j.ejmech.2016.09.059
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• Synthesis of Novel Triazole-incorporated Isatin Derivatives as Antifungal, Antitubercular, and Antioxidant Agents and Molecular Docking Study
  Journal of Heterocyclic Chemistry 2017 DOI: 10.1002/jhet.2598
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• 1,2,3-Triazole incorporated coumarin derivatives as potential antifungal and antioxidant agents
  Chinese Chemical Letters 2016 DOI: 10.1016/j.cclet.2015.11.003
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• 1,2,3-Triazole tethered acetophenones: Synthesis, bioevaluation and molecular docking study
  Chinese Chemical Letters 2016 DOI: 10.1016/j.cclet.2016.03.014
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• Facile synthesis of 1,3-thiazolidin-4-ones as antitubercular agents
  Bioorganic and Medicinal Chemistry Letters 2016 DOI: 10.1016/j.bmcl.2016.02.056
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• Facile synthesis of new N -sulfonamidyl-4-thiazolidinone derivatives and their biological evaluation
  New Journal of Chemistry 2016 DOI: 10.1039/c6nj00021e
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• Novel tetrazoloquinoline-rhodanine conjugates: Highly efficient synthesis and biological evaluation
  Bioorganic and Medicinal Chemistry Letters 2016 DOI: 10.1016/j.bmcl.2016.03.045
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• Novel tetrazoloquinoline-thiazolidinone conjugates as possible antitubercular agents: Synthesis and molecular docking
  MedChemComm 2016 DOI: 10.1039/c6md00278a
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