Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/487339
Full metadata record
DC FieldValueLanguage
dc.coverage.spatialBiological Important Heterocycles
dc.date.accessioned2023-05-30T11:09:08Z-
dc.date.available2023-05-30T11:09:08Z-
dc.identifier.urihttp://hdl.handle.net/10603/487339-
dc.description.abstractThe present work undertaken entitled Synthesis and Characterization of Some newlineBiological Important Heterocycles by Conventional and Non-conventional Methods is newlinepresented in six chapters and each chapter (from chapter II to V) is subdivided in to three section newlineA, B and C. The chapter wise summary is given below. newlineCHAPTER-I newlineINTRODUCTION newlineThe first part describes the general introduction and literature survey. newlineCHAPTER-II newlineSYNTHESIS OF 2, 4, 5-TRIPHENYLIMIDAZOLE DERIVATIVES And newlineSYNTHESIS OF 5-ARYLIDENE-2, 4-THIAZOLIDINEDIONES newlineIt is divided into three sections. newlineSECTION A newlineIn this section, 2, 4, 5-triphenylimidazole derivatives are prepared by reaction of newlinesubstitute benzaldehyde heterocyclic aldehydes, benzil/benzoin and ammonium acetate in newlinepresence of silicotungstic acid (STA) (7.5 mol %) as catalyst in ethanol solvent on reflux newline(Scheme-I). newlineScheme-I newlineSECTION B newlineIn this section, 2, 4, 5-triphenylimidazole derivatives are prepared by reaction of newlinesubstitute benzaldehyde heterocyclic aldehydes, benzil/benzoin and ammonium acetate in newlinepresence of L-Glutamic acid (10 mol %) catalyst in ethanol solvent on reflux (Scheme-II). newlineAbstract newlineB. P. Ankush 2 newlineScheme-II newlineSECTION C newlineIn this section we have studied, the synthesis of substituted 5-Benzylidenethiazolidine-2, newline4-dione derivatives from substituted benzaldehyde and thiazolidine-2, 4- dione in the presence of newlinecatalytic amount of tannic acid (10 mol %) in ethanol solvent at 80 °C temperature (Scheme-III). newlineScheme-III newlineCHAPTER-III newlineSYNTHESIS OF TETRAHYDROBENZO[b]PYRAN DERIVATIVES newlineIt is divided into three sections. newlineSECTION A newlineThis section deals with the synthesis of tetrahydrobenzo[b]pyran derivatives from newlinedifferent substituted benzaldehyde / heterocyclic aldehydes, dimedone and malononitrile by using newlinetannic acid (10 mol %) as catalyst in ethanol: water (1: 4) solvent on reflux (Scheme-IV). newlineScheme-IV newlineAbstract newlineB. P. Ankush 3 newlineSECTION B newlineIn this section, we have reported a facile and efficient methodology for the synthesis of newlinetetrahydrobenzo[b]pyran. This method involves the efficient synthesis of
dc.format.extent302p
dc.languageEnglish
dc.relation458b
dc.rightsuniversity
dc.titleSynthesis and Characterization of Some Biological Important Heterocycles by Conventional and Non Conventional Methods
dc.title.alternative
dc.creator.researcherAnkush Bhaskar Prabhakar
dc.subject.keywordChemistry
dc.subject.keywordChemistry Applied
dc.subject.keywordPhysical Sciences
dc.description.note
dc.contributor.guideShitole Nana Vikram
dc.publisher.placeNanded
dc.publisher.universitySwami Ramanand Teerth Marathwada University
dc.publisher.institutionDepartment of Chemistry
dc.date.registered2016
dc.date.completed2023
dc.date.awarded2023
dc.format.dimensions
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Department of Chemistry

Files in This Item:
File Description SizeFormat 
01_title.pdfAttached File265.59 kBAdobe PDFView/Open
02_preliminery pages.pdf652.55 kBAdobe PDFView/Open
03_contents.pdf207.1 kBAdobe PDFView/Open
04_abstract.pdf629.04 kBAdobe PDFView/Open
05_chapter 1.pdf889.16 kBAdobe PDFView/Open
06_chapter 2.pdf2.17 MBAdobe PDFView/Open
07_chapter 3.pdf1.94 MBAdobe PDFView/Open
08_chapter 4.pdf2.07 MBAdobe PDFView/Open
09_chapter 5.pdf2.02 MBAdobe PDFView/Open
10_chapter 6.pdf283.84 kBAdobe PDFView/Open
11_annexures, publications.pdf376.23 kBAdobe PDFView/Open
80_recommendation.pdf275.1 kBAdobe PDFView/Open


Items in Shodhganga are licensed under Creative Commons Licence Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0).

Altmetric Badge: