Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/472894
Title: Studies on the Ni Catalyzed Synthesis of Tertiary Amides and Pd Catalyzed Synthesis of and#945; Naphthol Based Triarylmethanes Ortho Arylated D Phenylglycine Methyl Esters and and#946; Arylated Keto Acids
Researcher: Sankar, Rathinam
Guide(s): Babu, S. Arulananda
Keywords: Life Sciences
Plant and Animal Science
Plant Sciences
University: Indian Institute of Science Education and Research (IISER) Mohali
Completed Date: 2018
Abstract: A literature survey revealed that the N-arylation and C-N bond formations have been well studied newlineusing Cu or Pd catalysts. Notably, the N-arylation and C-N bond formations have not been reported newlineusing Ni catalysts and a part of this thesis deals on the usage of nickel catalyst for the synthesis of newlinetertiary amides via N-arylation and C-N bond formation. Next, the C-C bond formation by Heck newlinecoupling reactions has significantly attracted the attention of chemists. Aryl sulphonyl chlorides newlinehave also been introduced in the place of aryl halides for performing the Heck reactions. In this newlineline, a part of this thesis work deals on synthesis of and#945;-naphthol-based triarylmethanes via Heck newlinecoupling reaction. In recent years, the transition metal-catalyzed directed C-H functionalization newlinereactions have emerged as one of the important synthetic organic transformations. In this line, a newlinepart of this thesis deals on the Pd-catalyzed bis-arylation of ortho C(sp 2 )-H bonds of D-(-)- newlinephenylglycine methyl esters and also and#946;-C(sp 3 )-H arylation of and#949;-, and#950;-, and#951;-keto acids. newlineThis thesis entitled Studies on the Ni-Catalyzed Synthesis of Tertiary Amides and Pd-Catalyzed newlineSynthesis of and#945;-Naphthol-Based Triarylmethanes, Ortho-Arylated D-(-)-Phenylglycine Methyl newlineEsters and and#946;-Arylated Keto Acids. newline
Pagination: 147p.
URI: http://hdl.handle.net/10603/472894
Appears in Departments:Department of Chemical Sciences

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02_preliminary pages.pdf146.91 kBAdobe PDFView/Open
03_content.pdf57.24 kBAdobe PDFView/Open
04_abstract.pdf69 kBAdobe PDFView/Open
05_chapter1.pdf2.22 MBAdobe PDFView/Open
06_chapter2.pdf2.25 MBAdobe PDFView/Open
07_chapter3.pdf1.92 MBAdobe PDFView/Open
08_chapter4.pdf1.52 MBAdobe PDFView/Open
09_annexures.pdf297.71 kBAdobe PDFView/Open
80_recommendation.pdf245.66 kBAdobe PDFView/Open
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