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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 |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
01_title.pdf | Attached File | 265.59 kB | Adobe PDF | View/Open |
02_preliminery pages.pdf | 652.55 kB | Adobe PDF | View/Open | |
03_contents.pdf | 207.1 kB | Adobe PDF | View/Open | |
04_abstract.pdf | 629.04 kB | Adobe PDF | View/Open | |
05_chapter 1.pdf | 889.16 kB | Adobe PDF | View/Open | |
06_chapter 2.pdf | 2.17 MB | Adobe PDF | View/Open | |
07_chapter 3.pdf | 1.94 MB | Adobe PDF | View/Open | |
08_chapter 4.pdf | 2.07 MB | Adobe PDF | View/Open | |
09_chapter 5.pdf | 2.02 MB | Adobe PDF | View/Open | |
10_chapter 6.pdf | 283.84 kB | Adobe PDF | View/Open | |
11_annexures, publications.pdf | 376.23 kB | Adobe PDF | View/Open | |
80_recommendation.pdf | 275.1 kB | Adobe PDF | View/Open |
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