Department Researches & Publications

Department of chemistry

Researches

The department has a strategic plan for future research which contributes to the prosperity of the society. We foster world-class research and outstanding chemical education, as well as we strengthen our students, faculty, staff, and alumni to interact with the local, national, and global community.

Research Groups:

  • Organic Chemistry
  • Inorganic Chemistry
  • Analytical Chemistry
  • Electro analytical Chemistry
  • Molecular Spectroscopy
  • Electrochemistry
  • Surface Chemistry and Catalysis
  • Theoretical Chemistry

 

# Title Research Year
501 Synthesis, Reactions, and Antimicrobial Activity of Novel Heterocyclic Compounds Containing Cyclopenta[d]thieno[2,3-b]pyridine Moiety and Related Fused Heterocycles 2020
502 Synthesis, reactions, and spectral characterization of some new biologically active compounds derived from thieno[2,3-c]pyrazole-5-carboxamide 2020
503 Synthesis, reactions, and spectral characterization of some new biologically active compounds derived from thieno[2,3-c]pyrazole-5-carboxamide 2020
504 Synthesis, reactions, and spectral characterization of some new biologically active compounds derived from thieno[2,3-c]pyrazole-5-carboxamide 2020
505 Synthesis, reactions, and spectral characterization of some new biologically active compounds derived from thieno[2,3-c]pyrazole-5-carboxamide 2020
506 Synthesis, spectroscopic characterization, and in vitro antimicrobial activity of fused pyrazolo[4′,3′:4,5]thieno[3,2‐d]pyrimidine 2020
507 Synthesis, spectroscopic characterization, and in vitro antimicrobial activity of fused pyrazolo[4′,3′:4,5]thieno[3,2‐d]pyrimidine 2020
508 Synthesis, spectroscopic characterization, and in vitro antimicrobial activity of fused pyrazolo[4′,3′:4,5]thieno[3,2‐d]pyrimidine 2020
509 Synthesis, spectroscopic characterization, and in vitro antimicrobial activity of fused pyrazolo[4′,3′:4,5]thieno[3,2‐d]pyrimidine 2020
510 Target-oriented synthesis of functionalized pyrazolo-fused medium-sized N, S-heterocycles via Friedel–Crafts ring closure approach 2020