Please use this identifier to cite or link to this item:
Title: Strategies for the Synthesis of New Chiral Pyrrolidine Based Organocatalytic Asymmetric CC Bond Formation Reactions
Researcher: Chakarawar Avinash V.
Guide(s): Bhusare S. R.
Keywords: Physical Sciences,Chemistry,Chemistry Analytical
University: Swami Ramanand Teerth Marathwada University
Completed Date: 28/09/2018
Abstract: In the present work, we have synthesized two new chiral pyrrolidine based newlineorganocatalysts and studied it s applications in the different organocatalytic newlineasymmetric C-C bond formation reactions for the synthesis of some heterocyclic newlinecompounds. The thesis work is divided into five chapters. The first chapter is divided newlineinto two sections, Section A deals with the introduction to field of organocatalysis and newlineSection B describes the synthesis and characterization of new chiral pyrrolidine based newlineorganocatalysts. Applications of these catalysts were studied in different chemical newlinetransformations i.e. organocatalytic asymmetric C-C bond formation reactions. newlineSecond chapter deals with the study of asymmetric synthesis of xanthenone newlinecompounds. It is divided into two sections, each section describing the details of the newlineasymmetric synthesis of one family of xanthenone skeleton. The third chapter is newlinedivided into two sections, Section A describes asymmetric synthesis of newlinebenzo[a]xanthene-11-one and benzo[a]acridine-11-one derivatives. Section B newlinedescribes asymmetric synthesis of dihydropyrano (c) chromene and pyrano [2,3-d]- newlinepyrimidine derivatives.. Chapter four is grouped into two sections: section A deals newlinewith organocatalytic enantioselective synthesis of optically active 7-aryl-11,12- newlinedihydrobenzo [H] pyrimido-[4,5-b]quinoline-8,10(7H,9H)-diones and organocatalytic newlineasymmetric synthesis of chromenyl phosphonates and dicyanophenylethyl newlinephosphonates was studied in section B. Asymmetric pyrrolidine based organocatalytic newline newline
Pagination: 202p
Appears in Departments:Department of Chemistry

Files in This Item:
File Description SizeFormat 
01_title.pdfAttached File10.2 kBAdobe PDFView/Open
02_certificate.pdf7.34 kBAdobe PDFView/Open
03_abstract.pdf163.51 kBAdobe PDFView/Open
04_decalaration.pdf7.38 kBAdobe PDFView/Open
05_acknowledgement.pdf23.24 kBAdobe PDFView/Open
06_contents.pdf67.42 kBAdobe PDFView/Open
07_list_of_tables.pdf51.93 kBAdobe PDFView/Open
08_list_of_figure.pdf9.87 kBAdobe PDFView/Open
09_abbreviations.pdf13.9 kBAdobe PDFView/Open
10_chapter 1.pdf1.28 MBAdobe PDFView/Open
11_chapter 2.pdf7.09 MBAdobe PDFView/Open
12_chapter 3.pdf1.47 MBAdobe PDFView/Open
13_chapter 4.pdf1.44 MBAdobe PDFView/Open
14_chapter 5.pdf2.32 MBAdobe PDFView/Open
15_conclusion.pdf16.94 kBAdobe PDFView/Open
16_bibliography.pdf204.15 kBAdobe PDFView/Open

Items in Shodhganga are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetric Badge: