Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/383028
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dc.coverage.spatialmulti component reactions
dc.date.accessioned2022-05-31T06:04:15Z-
dc.date.available2022-05-31T06:04:15Z-
dc.identifier.urihttp://hdl.handle.net/10603/383028-
dc.description.abstractStudies on multi-component reactions for the Synthesis of Biologically Active Compounds. newlineChapter 1: Synthesis of 1-phenyl isoquinoline derivatives and synthesis of newline4,4 (arylmethelene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ols). newlineSection 1.1: Synthesis of 1-phenyl isoquinoline derivatives. newlineSection 1.2: Synthesis of 4,4 (arylmethelene) bis (3-methyl-1H pyrazol-5-ols). newlineChapter 2: Synthesis of Quinoxaline derivatives. newlineSection 2.1 : Synthesis of Quinoxaline from ortho phenelene diamine and phenacyl newlinebromide. newlineSection 2.2 : Synthesis of Quinoxaline from ortho phenelene diamine and 1,2 newlinediketones. newlineChapter 3: Synthesis of Pyrido [2,3-d : 6,5-d] dipyrimidine and Spiro-oxoindole newlinederivatives newlineSection 3.1 : Synthesis of Pyrido [2,3-d : 6,5-d] dipyrimidine derivatives newlineSection 3.2: Synthesis of Spiro-oxoindole derivatives newlineChapter 4: Synthesis of 3 methyl 4 - benzyl methelene-isoxazol 5(4H) ones newlineand Dielectric Dispersion study of Isoxazol Derivatives with binary newlinemixtures of DMSO. newlineSection 4.1 : Synthesis of 3 methyl 4 - benzyl methelene-isoxazol 5(4H) ones. newlineSection 4.2 : Dielectric Dispersion Study of Isoxazol Derivatives with Binary Mixture newlineof DMSO. newlineChapter 5: Biological activity of synthesized compound. newlineSection 5.1 : 3 methyl- 4 - benzyl methelene-isoxazol 5(4H) ones. newlineSection 5.2 : 4,4 ( aryl methelene) bis (3-methyl-1-phenyl-1H-Pyrazol-5 ols) newlinederivatives newlineSection 5.3 : 1-Phenyl isoquinoline derivatives newlineSection 5.4: Synthesis of Spiro-oxoindole derivatives newlineSection 5.5 : Pyrido [2,3-d : 6,5-d] dipyrimidine derivatives newlineABSTRACT newlineIn the present work, we have synthesized bioactive heterocyclic compounds using green protocol as well as drastic conditions in multistep reactions and their biological activities have been studied. The work is divided into five chapters. newlineThe first chapter includes the synthesis of 1-phenyl isoquinoline derivatives and synthesis of 4,4 ( aryl methelene) bis (3-methyl-1-phenyl-1H-Pyrazol-5 ols) derivatives and it is divided into to two sections. Section 1 describes the extraordinary ruthenium cata
dc.format.extent226p
dc.languageEnglish
dc.relation40b
dc.rightsuniversity
dc.titleStudies on Multi Component Reactions for the Synthesis of Biologically Active Compounds
dc.title.alternative
dc.creator.researcherNakkalwar Shrinivas Lingagoud
dc.subject.keywordChemistry
dc.subject.keywordChemistry Applied
dc.subject.keywordPhysical Sciences
dc.description.note
dc.contributor.guidePatwari Shivaji B.
dc.publisher.placeNanded
dc.publisher.universitySwami Ramanand Teerth Marathwada University
dc.publisher.institutionDepartment of Chemistry
dc.date.registered2014
dc.date.completed2021
dc.date.awarded2022
dc.format.dimensions
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Department of Chemistry

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01_title.pdfAttached File226.43 kBAdobe PDFView/Open
02_certificate.pdf136.05 kBAdobe PDFView/Open
03_abstract.pdf266.83 kBAdobe PDFView/Open
04_decleration.pdf62.07 kBAdobe PDFView/Open
05_acknowledgement.pdf55.79 kBAdobe PDFView/Open
06_contents.pdf83.71 kBAdobe PDFView/Open
07_abbreviations.pdf91.31 kBAdobe PDFView/Open
08_chapter 1.pdf2.45 MBAdobe PDFView/Open
09_chapter 2.pdf1.44 MBAdobe PDFView/Open
10_chapter 3.pdf2.35 MBAdobe PDFView/Open
11_chapter 4.pdf1.68 MBAdobe PDFView/Open
12_chapter 5.pdf587.98 kBAdobe PDFView/Open
13_conclusion.pdf91.02 kBAdobe PDFView/Open
14-bibilography.pdf107.64 kBAdobe PDFView/Open
80_recommendation.pdf469.43 kBAdobe PDFView/Open


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