Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/257555
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dc.coverage.spatialchemistry
dc.date.accessioned2019-09-12T11:16:18Z-
dc.date.available2019-09-12T11:16:18Z-
dc.identifier.urihttp://hdl.handle.net/10603/257555-
dc.description.abstractChemistry of heterocycles has been widely studied because of their wide range newlineof applications as pharmaceuticals, agrochemicals and veterinary products. They are newlinehaving a wide range of application such as sanitizers, antioxidants, anti-malarial, and newlineanti-diabetics. newlineThis thesis mainly focus on synthesis and biological activity studies of new newlineheterocycles having five, six and seven-membered rings and containing heteroatoms newlinenitrogen (N), oxygen (O), or sulfur (S). The best known of the five-membered ring newlineheterocyclic compounds are pyrazoline contains a ring of five atoms, three are carbon newlineatoms and two nitrogen atoms, isoxazoline contains a ring of five atoms, three carbon newlineatoms, one nitrogen and one oxygen atoms. The six-member heterocyclic compounds newlineare pyridine contains a ring of six atoms-five carbon atoms and one nitrogen atom, newlinepyrimidine contains a ring of six atoms-four carbon atoms and two nitrogen atom and newlineseven member heterocyclic compounds are benzodiazipine contains a ring of seven newlineatoms-five carbon atoms and two nitrogen atom and benzothiazipines contains a ring newlineof seven atoms-five carbon atoms, one nitrogen and one sulfur atom. newlineThe heterocyclic compounds such as pyrazol, isoxazol, pyridine, pyrimidine, newlinebenzodizipine and benzothiazipines are synthesized from and#945;, and#946;-unsaturated ketones newlineexhibited a vide range of activities such as antimicrobial, anticancer, anti-tubercular, newlineanti-diabetics, anticonvulsant, antioxidant and anti-inflammatory. newlineHowever, the halogen substituted heterocycles of these categories is not newlinereported and studied much. Hence, due to miscellaneous applications of such different newlineheterocyclic compounds and their derivatives encouraged us to work in the area of newlineheterocyclic chemistry. Consequently, the present work describes the synthesis and newlinebiological activity studies such as different derivatives of chalcones, pyrazolines, newlineisoxazolines, pyridines, pyrimidines, benzodizipines and benzothiazipines. The newlineextension of this work has scope for novel improved synthetic modes for a wide newlinevariety of
dc.format.extent241p
dc.languageEnglish
dc.relation403b
dc.rightsuniversity
dc.titleSynthesis and Study of Some New Heterocyclic Compounds and their Applications
dc.title.alternativen.a.
dc.creator.researcherVidule Ravikumar Ramlu
dc.subject.keywordPhysical Sciences,Chemistry,Chemistry Analytical
dc.description.noteBibliography
dc.contributor.guideMohammad Abdul Baseer
dc.publisher.placeNanded
dc.publisher.universitySwami Ramanand Teerth Marathwada University
dc.publisher.institutionSchool of Chemical Sciences
dc.date.registered05/08/2014
dc.date.completed24/09/2018
dc.date.awarded22/01/2019
dc.format.dimensions
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:School of Chemical Sciences

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01_title.pdfAttached File8.98 kBAdobe PDFView/Open
02_certificate.pdf11.79 kBAdobe PDFView/Open
03_abstract.pdf260.72 kBAdobe PDFView/Open
04_declaration.pdf11.73 kBAdobe PDFView/Open
05_acknowledgement.pdf17.32 kBAdobe PDFView/Open
06_contents.pdf11.81 kBAdobe PDFView/Open
07_list_of_tables.pdf7.03 kBAdobe PDFView/Open
08_list_of_figures.pdf5.21 kBAdobe PDFView/Open
09_chapter 1.pdf1.51 MBAdobe PDFView/Open
10_chapter 2.pdf1.33 MBAdobe PDFView/Open
11_chapter 3.pdf1.53 MBAdobe PDFView/Open
12_chapter 4.pdf1.03 MBAdobe PDFView/Open
13_chapter 5.pdf1.64 MBAdobe PDFView/Open
14_chapter 6.pdf1.76 MBAdobe PDFView/Open
15_chapter 7.pdf1.26 MBAdobe PDFView/Open
16_chapter 8a.pdf5.87 MBAdobe PDFView/Open
17_chapter 8b.pdf183.73 kBAdobe PDFView/Open
18_conclusion.pdf11.99 kBAdobe PDFView/Open
19_summery.pdf9.17 kBAdobe PDFView/Open
20_bibliography.pdf164.96 kBAdobe PDFView/Open


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