Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/397587
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dc.date.accessioned2022-08-05T05:42:38Z-
dc.date.available2022-08-05T05:42:38Z-
dc.identifier.urihttp://hdl.handle.net/10603/397587-
dc.description.abstractIn 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
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dc.languageEnglish
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dc.rightsuniversity
dc.titleMetal Free Synthesis of Aromatic Heterocycles and Biological Evaluation of Heterocyclic Hybrid Molecules
dc.title.alternative
dc.creator.researcherRamu, S
dc.subject.keywordChemistry
dc.subject.keywordChemistry Applied
dc.subject.keywordPhysical Sciences
dc.description.note
dc.contributor.guideBaburaj Baskar
dc.publisher.placeKattankulathur
dc.publisher.universitySRM Institute of Science and Technology
dc.publisher.institutionDepartment of Chemistry
dc.date.registered
dc.date.completed2022
dc.date.awarded
dc.format.dimensions
dc.format.accompanyingmaterialDVD
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Department of Chemistry

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02_declaration.pdf402.3 kBAdobe PDFView/Open
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04_acknowledgement.pdf501.71 kBAdobe PDFView/Open
05_content.pdf569.73 kBAdobe PDFView/Open
06_list of graph and table.pdf536.43 kBAdobe PDFView/Open
07_abstract.pdf405.89 kBAdobe PDFView/Open
08_chapter 1.pdf971.4 kBAdobe PDFView/Open
09_chapter 2.pdf407.66 kBAdobe PDFView/Open
10_chapter 3.pdf7.96 MBAdobe PDFView/Open
11_chapter 4.pdf2.26 MBAdobe PDFView/Open
12_chapter 5.pdf1.78 MBAdobe PDFView/Open
13_chapter 6.pdf524.31 kBAdobe PDFView/Open
14_references.pdf577.5 kBAdobe PDFView/Open
15_list of publications.pdf401.56 kBAdobe PDFView/Open
16_vitae.pdf279.02 kBAdobe PDFView/Open
80_recommendation.pdf557.89 kBAdobe PDFView/Open


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