Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/253107
Title: Synthesis characterization spectral hammett application and biological activities of some chalcones
Researcher: Usha V
Guide(s): Thangaraj V
Keywords: Hammett
Physical Sciences,Chemistry,Chemistry Analytical
Synthesis
University: Anna University
Completed Date: 2018
Abstract: One of the main objectives of organic and medicinal chemistry is newlinethe sensible design, synthesis and production of molecules having value as newlinehuman therapeutic agents. Organic molecules containing aromatic rings are newlinewidely distributed in nature and often play an important role in various newlinebiochemical processes. A number of such compounds find applications in newlinevarious fields ranging from drugs, medicines, dyes and so on. Structureactivity newlinerelationship studies often reveal chemical and biochemical reactivity newlineof these compounds and therefore alter their metabolism.In this work, about five series of (2E)-aryl enones such as 2-benzofuranyl, 3-chloro-4-nitrophenyl, 3-nitro-4-chlorophenyl, 2-pyrenyl and 3-phenanthryl chalcones have been synthesized by crossed Aldol condensation of substituted benzaldehydes and the above mentioned aryl newlinemethyl ketone using microwave irradiation and ultrasonic techniques with newlineFeCl3/Bentonite and Sodium hydroxide as catalysts. This thesis deals with the newlinesynthesis, characterization, correlation and biological evaluation of all the newlinesynthesized compounds. It consists of nine chapters. The first chapter newlineprovides the main aim of the work, research objectives, a literature survey of newlinethe present work and the framework for the whole thesis. Chapter two newlineelaborately discusses the various methods of characterization techniques used newlinefor this work. Chapter three discusses the materials and methods used for this newlinework. Chapter four provides the synthesis of substituted newlinestyryl 2-benzofuranyl ketone by ultrasonication method. newline newline
Pagination: xxxii, 210p.
URI: http://hdl.handle.net/10603/253107
Appears in Departments:Faculty of Science and Humanities

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01_title.pdfAttached File336.52 kBAdobe PDFView/Open
02_certificates.pdf764.5 kBAdobe PDFView/Open
03_abstract.pdf330.87 kBAdobe PDFView/Open
04_acknowledgment.pdf233.2 kBAdobe PDFView/Open
05_contents.pdf390.59 kBAdobe PDFView/Open
06_chapter1.pdf837.31 kBAdobe PDFView/Open
07_chapter2.pdf662.81 kBAdobe PDFView/Open
08_chapter3.pdf776.33 kBAdobe PDFView/Open
09_chapter4.pdf2.19 MBAdobe PDFView/Open
10_chapter5.pdf1.55 MBAdobe PDFView/Open
11_chapter6.pdf1.53 MBAdobe PDFView/Open
12_chapter7.pdf1.54 MBAdobe PDFView/Open
13_chapter8.pdf1.47 MBAdobe PDFView/Open
14_conclusion.pdf522.44 kBAdobe PDFView/Open
15_references.pdf801.3 kBAdobe PDFView/Open
16_publications.pdf481.15 kBAdobe PDFView/Open
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