Please use this identifier to cite or link to this item:
http://hdl.handle.net/10603/397587
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DC Field | Value | Language |
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dc.coverage.spatial | ||
dc.date.accessioned | 2022-08-05T05:42:38Z | - |
dc.date.available | 2022-08-05T05:42:38Z | - |
dc.identifier.uri | http://hdl.handle.net/10603/397587 | - |
dc.description.abstract | In the present study, we have demonstrated for the first time a simple and environmentally friendly strategy towards production of and#946;-carbolines using a domino Pictet-Spengler reaction and aromatization in O2 atm in NMP. The reaction takes place in a metal-free solvent-promoted system at 140 °C in an oxygen atmosphere, and it works without the need of any base or additives. The reaction was found to be appropriate for the production of and#946;-carboline esters, and#946;-carbolines. Furthermore, the same reaction was carried out in an Ar atm with a catalytic amount of 4-nitrobenzoic acid in NMP produced THand#946;C s. Additionally, the scope of the reaction methodology was also extended for the total production of and#946;-carboline based natural products with biological importance newline | |
dc.format.extent | ||
dc.language | English | |
dc.relation | ||
dc.rights | university | |
dc.title | Metal Free Synthesis of Aromatic Heterocycles and Biological Evaluation of Heterocyclic Hybrid Molecules | |
dc.title.alternative | ||
dc.creator.researcher | Ramu, S | |
dc.subject.keyword | Chemistry | |
dc.subject.keyword | Chemistry Applied | |
dc.subject.keyword | Physical Sciences | |
dc.description.note | ||
dc.contributor.guide | Baburaj Baskar | |
dc.publisher.place | Kattankulathur | |
dc.publisher.university | SRM Institute of Science and Technology | |
dc.publisher.institution | Department of Chemistry | |
dc.date.registered | ||
dc.date.completed | 2022 | |
dc.date.awarded | ||
dc.format.dimensions | ||
dc.format.accompanyingmaterial | DVD | |
dc.source.university | University | |
dc.type.degree | Ph.D. | |
Appears in Departments: | Department of Chemistry |
Files in This Item:
File | Description | Size | Format | |
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01_title.pdf | Attached File | 167.08 kB | Adobe PDF | View/Open |
02_declaration.pdf | 402.3 kB | Adobe PDF | View/Open | |
03_certificate.pdf | 408.25 kB | Adobe PDF | View/Open | |
04_acknowledgement.pdf | 501.71 kB | Adobe PDF | View/Open | |
05_content.pdf | 569.73 kB | Adobe PDF | View/Open | |
06_list of graph and table.pdf | 536.43 kB | Adobe PDF | View/Open | |
07_abstract.pdf | 405.89 kB | Adobe PDF | View/Open | |
08_chapter 1.pdf | 971.4 kB | Adobe PDF | View/Open | |
09_chapter 2.pdf | 407.66 kB | Adobe PDF | View/Open | |
10_chapter 3.pdf | 7.96 MB | Adobe PDF | View/Open | |
11_chapter 4.pdf | 2.26 MB | Adobe PDF | View/Open | |
12_chapter 5.pdf | 1.78 MB | Adobe PDF | View/Open | |
13_chapter 6.pdf | 524.31 kB | Adobe PDF | View/Open | |
14_references.pdf | 577.5 kB | Adobe PDF | View/Open | |
15_list of publications.pdf | 401.56 kB | Adobe PDF | View/Open | |
16_vitae.pdf | 279.02 kB | Adobe PDF | View/Open | |
80_recommendation.pdf | 557.89 kB | Adobe PDF | View/Open |
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