Please use this identifier to cite or link to this item:
http://hdl.handle.net/10603/359224
Title: | Asymmetric Synthesis of 3 3 Disubstituted Oxindoles and Spirocyclic Oxindoles |
Researcher: | Hazra, Atanu |
Guide(s): | Ray, Biswajit and Hajra, Saumen |
Keywords: | Chemistry Chemistry Inorganic and Nuclear Physical Sciences |
University: | Banaras Hindu University |
Completed Date: | 2020 |
Abstract: | The chiral 3,3-disubstituted / spiro-oxindole framework is considered as a privileged heterocyclic motif. The enantiopure 3,3-disubstituted / spiro oxindole motif is present in many bioactive natural products and a series of pharmaceutically active compounds hence has gained significant attention by medicinal as well as synthetic chemists. These significant bioactivities and versatility newlineof 3,3-disubstituted / spiro-oxindole bearing natural products, drugs, and related analogs propelled us to develop newer methodologies for the asymmetric synthesis of 3,3-disubstituted oxindole and some important natural product and drug leads. newline |
Pagination: | |
URI: | http://hdl.handle.net/10603/359224 |
Appears in Departments: | Department of Chemistry |
Files in This Item:
File | Description | Size | Format | |
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01_title.pdf | Attached File | 194.54 kB | Adobe PDF | View/Open |
02_certificate.pdf | 399.69 kB | Adobe PDF | View/Open | |
03_content.pdf | 396.19 kB | Adobe PDF | View/Open | |
04_abstract.pdf | 468.38 kB | Adobe PDF | View/Open | |
05_acknowledgement.pdf | 124.99 kB | Adobe PDF | View/Open | |
06_abbreviation.pdf | 119.84 kB | Adobe PDF | View/Open | |
07_preface.pdf | 114.89 kB | Adobe PDF | View/Open | |
08_chapter1.pdf | 1.51 MB | Adobe PDF | View/Open | |
09_chapter2.pdf | 6.6 MB | Adobe PDF | View/Open | |
10_chapter3.pdf | 15.02 MB | Adobe PDF | View/Open | |
11_appendices.pdf | 4.99 MB | Adobe PDF | View/Open | |
80_recommendation.pdf | 704.12 kB | Adobe PDF | View/Open |
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