Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/261491
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dc.coverage.spatialScience
dc.date.accessioned2019-10-11T06:03:25Z-
dc.date.available2019-10-11T06:03:25Z-
dc.identifier.urihttp://hdl.handle.net/10603/261491-
dc.description.abstractIn the present work, we have tried to articulate and boost new organic articles by linking several different kinds of substituted coumarin with previously prepared aniline mustard and simple N-nitrogen mustard. Each of the derived molecules was characterized by the progressive structural interpretation techniques like 1H NMR, IR, and Mass spectroscopy. The purity of all organic compounds was tested by the routine chromatographic method. Each of the newly synthesized molecules was put forward for their anticancer activity where Human Colon Cancer Cell Line Colo-205 Cell line was tested, effectively six compounds were found to be equally potent to the commercially available drug (Adriamycin) for the in-vitro condition. newline
dc.format.extent-
dc.languageEnglish
dc.relationNo. of References 172
dc.rightsuniversity
dc.titleStudies on and#946; and#946; dichlorodiethyl amine derivatives
dc.title.alternative
dc.creator.researcherBarasara, A.P.
dc.subject.keywordAnticancer activities
dc.subject.keywordChromatography
dc.subject.keywordCoumarin
dc.subject.keywordHeterocyclic
dc.subject.keywordMustard
dc.subject.keywordNMR Spectroscopy
dc.subject.keywordPhysical Sciences,Chemistry,Chemistry Applied
dc.subject.keywordPyrazolo aldehyde
dc.subject.keywordSchiffs base
dc.description.noteReferences p. 136-146, Appendix p. 174-150
dc.contributor.guideBhatt, H.
dc.publisher.placeRajkot
dc.publisher.universityRK University
dc.publisher.institutionFaculty of Science
dc.date.registered01/01/2014
dc.date.completed20/08/2019
dc.date.awarded14/10/2019
dc.format.dimensions-
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Faculty of Science

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01_cover page.pdfAttached File74.15 kBAdobe PDFView/Open
04_ acknowledgement.pdf72.18 kBAdobe PDFView/Open
08_list of abbreviations.pdf76.03 kBAdobe PDFView/Open
09_abstract.pdf60.49 kBAdobe PDFView/Open
10_graphical abstract.pdf145.88 kBAdobe PDFView/Open
11_chepter 1.pdf1.19 MBAdobe PDFView/Open
12_chepter 2.pdf1.3 MBAdobe PDFView/Open
15_list of publication.pdf827.16 kBAdobe PDFView/Open
16_references.pdf182.8 kBAdobe PDFView/Open
17_appendix.pdf827.16 kBAdobe PDFView/Open


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