Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/17568
Title: Synthesis, characterization and biological invstigations of new imidazolinones derivatives
Researcher: Patel, Ameebahen Babulal
Guide(s): Patel, Pankajkumar S
Keywords: Chemistry
Imidazolone Derivatives
Chalcone Derivatives
Upload Date: 1-Apr-2014
University: Shri Jagdishprasad Jhabarmal Tibarewala University
Completed Date: 23/08/2013
Abstract: Heterocyclic Chemistry, a chemical, a branch processing synthesis, Properties, and applications heterocycles. Heterocyclic compounds the classification is probably the largest and the most experienced of organotin compounds, and, after all, each carbocyclic compounds, structure and function, it may be in principle, can be converted to a collection are a number of similarities between the heterocyclic rings by replacing one or more of the ring of carbon atoms with a different element, even if we are to restrict our consideration of oxygen, nitrogen and sulfur, permutations and combinations, which replace many. The main objective of the medicinal chemistry is the design and discovery of new compounds, and is suitable for use of the drug this process requires team efforts. It not only involve chemists but also workers from a broad range of disciplines that,biology, biochemistry, pharmacology, computing and medicine in other. Chemical for the pharmaceutically important compounds is mainly divided into two parts, the first chemotherapy, concerned about the treatment of the infection, and parasitic diseases or malignant diseases of chemical Agents, usually material , shows the selective toxicity of the pathogens, the other Division related to diseases of the physical disorders and the agent to be employed in the main compounds The results of the operations of the economic recovery, and transmission of the nerve impulses or the action of hormone the receptor.
Pagination: 416p.
URI: http://hdl.handle.net/10603/17568
Appears in Departments:Faculty of Sciences

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02_declaration by the condidate.pdf25.5 kBAdobe PDFView/Open
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04_acknowledgement.pdf21.61 kBAdobe PDFView/Open
05_table of conent.pdf25.22 kBAdobe PDFView/Open
06_abstract.pdf13.61 kBAdobe PDFView/Open
07_chapter-1.pdf4.29 MBAdobe PDFView/Open
08_chapter-2.pdf4.29 MBAdobe PDFView/Open
09_chapter-3.pdf4.29 MBAdobe PDFView/Open
10_chapter-4.pdf4.29 MBAdobe PDFView/Open
11_chapter-5.pdf4.29 MBAdobe PDFView/Open
12_references.pdf4.3 MBAdobe PDFView/Open
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