Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/558188
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dc.date.accessioned2024-04-17T06:36:17Z-
dc.date.available2024-04-17T06:36:17Z-
dc.identifier.urihttp://hdl.handle.net/10603/558188-
dc.description.abstractTo see the potential applications of 1,3,4-trisubstituted pyrazoles in the various newlinefields and with the aim to enhance the biological activities, there is much scope to explore newlinethe synthetic approaches for the construction of the desired 1,3,4-trisubstituted newlinepyrazole derivatives. First, it is claimed that 1,3,4-trisubstituted pyrazoles with an acyl newlinefunctionality connected to the 4- position of the pyrazole scaffolds may be synthesized newlineeffectively and practically. By first forming an oxime, followed by a reaction with the newlineVilsmeier-Haack reagent, the precursor 4- cyanopyrazoles used to make the target newlinecompounds were created. 4-cyanopyrazoles produced the corresponding 1,3,4- newlinetrisubstituted pyrazoles in a 71 88% yield when they were combined with different newlineGrignard reagents. newline
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dc.languageEnglish
dc.relation
dc.rightsuniversity
dc.titleStudy of Synthetic Approaches of Same 1 3 4 Trisubstituted Pyrazole Derivatives
dc.title.alternative
dc.creator.researcherKumar, Parmod
dc.subject.keywordChemistry
dc.subject.keywordChemistry Applied
dc.subject.keywordPhysical Sciences
dc.description.note
dc.contributor.guideArif, Rizwan and Kumar, Anil
dc.publisher.placeFaridabad
dc.publisher.universityLingayas Vidyapeeth
dc.publisher.institutionSchool of Basic and Applied Science
dc.date.registered2020
dc.date.completed2024
dc.date.awarded2024
dc.format.dimensions
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:School of Basic and Applied Science

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01 title.pdfAttached File21.71 kBAdobe PDFView/Open
02 prelim pages.pdf419.71 kBAdobe PDFView/Open
03 content.pdf47.41 kBAdobe PDFView/Open
04 abstract.pdf160.29 kBAdobe PDFView/Open
05 chapter 1.pdf1.26 MBAdobe PDFView/Open
06 chapter 2.pdf2.6 MBAdobe PDFView/Open
07 chapter 3.pdf1.11 MBAdobe PDFView/Open
08 chapter 4.pdf1.4 MBAdobe PDFView/Open
09 chapter 5.pdf612.36 kBAdobe PDFView/Open
10 annexures.pdf4.1 MBAdobe PDFView/Open
80_recommendation.pdf626.78 kBAdobe PDFView/Open


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