Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/487339
Title: Synthesis and Characterization of Some Biological Important Heterocycles by Conventional and Non Conventional Methods
Researcher: Ankush Bhaskar Prabhakar
Guide(s): Shitole Nana Vikram
Keywords: Chemistry
Chemistry Applied
Physical Sciences
University: Swami Ramanand Teerth Marathwada University
Completed Date: 2023
Abstract: The 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
Pagination: 302p
URI: http://hdl.handle.net/10603/487339
Appears in Departments:Department of Chemistry

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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
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