Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/2874
Title: Synthesis and studies of some new heterocyclic compounds
Researcher: Kaur, Ramandeep
Guide(s): Kaur, Balbir
Keywords: Chemistry
Heterocyclic compounds
Upload Date: 5-Oct-2011
University: Punjabi University
Completed Date: 17/01/2011
Abstract: The work incorporated in this thesis entitled „Synthesis andStudies of Some New Heterocyclic Compounds’ involves the synthesis of novel Quinazoline and Pyrimidine derivatives. Literature study reveals that these derivatives show different biological activities viz. antitubercular, analgesic, anti-inflammatory, anti-bacterial, antimalarial, anti-fungal, anti-tumour, anti-HIV etc. This has prompted us to work on this category of compounds. Therefore, in search of new fused heterocyclic compounds with potential pharmaceutical value and in association with our work on the application of microwave irradiations, we synthesized (1) 4-aryl-3,4,5,6-tetrahydrobenzo[h] quinazoline-2(1H)-thiones; (2) 2-(alkyl/aralkylthio)-4-aryl-1,4,5,6- tetrahydrobenzo[h]quinazolines; (3) 1,4-diaryl-1,4,5,6tetrahydrobenzo [h]quinazoline-2-thiols; (4) 4-aryl-1,3,4,5-tetrahydro-2H-indeno[1,2- d]pyrimidine-2-thiones; (5) 2-(alkyl/araalkylthio)-4-aryl-4,5-dihydro- 1H-indeno[1,2-d] pyrimidines; (6) 1,4-diaryl-4,5-dihydro-1Hindeno[ 1,2-d]pyrimidine-2-thiols and their derivatives. Besides the synthetic part, some of the derivatives were screened for anti-bacterial activities. The antibacterial efficacy of the most effective extracts was compared with those of existing standard antibacterial antibiotics. Viz Amoxycillin and Ciprofloxacin. Seven different bacterial strains which were used as test organisms are: Pseudomonas fluorescence, Staphylococcus aureus, Acenetobactersp.,Bacillus subtilis, Staphylococcus epidermis, Salmonellatyphimurium TA 98, Escherichia coli
Pagination: 260p.
URI: http://hdl.handle.net/10603/2874
Appears in Departments:Department of Chemistry

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01_title.pdfAttached File51.52 kBAdobe PDFView/Open
02_abstract.pdf198.36 kBAdobe PDFView/Open
03_dedication.pdf18.78 kBAdobe PDFView/Open
04_certificate.pdf120.61 kBAdobe PDFView/Open
05_declaration.pdf76.93 kBAdobe PDFView/Open
06_acknowledgements.pdf16.47 kBAdobe PDFView/Open
07_contents.pdf174.1 kBAdobe PDFView/Open
08_list of publications.pdf102.87 kBAdobe PDFView/Open
09_introduction.pdf472.8 kBAdobe PDFView/Open
10_chapter 1.pdf367.5 kBAdobe PDFView/Open
11_chapter 2.pdf322.09 kBAdobe PDFView/Open
12_chapter 3.pdf381.71 kBAdobe PDFView/Open
13_chapter 4.pdf363.25 kBAdobe PDFView/Open
14_chapter 5.pdf789.67 kBAdobe PDFView/Open
15_summary.pdf425.98 kBAdobe PDFView/Open
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