Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/19277
Title: Stereoselective Total Synthesis of Biologically Active Natural Products Achaetolide Panaxjapyne C, Goniothalesdiol A and ( 5 R, 6 S)- Acetoxyhexadecanolide
Researcher: Thakur, Pallavi
Guide(s): Bandichhor, Rakeshwar
Mukkanti, K
Keywords: Acetoxyhexadecanolide
Active
Biologically
Goniothalesdio
Stereoselective
Synthesis
Upload Date: 13-Jun-2014
University: Jawaharlal Nehru Technological University, Hyderabad
Completed Date: 2013
Abstract: The Thesis entitled STEREOSELECTIVE TOTAL SYNTHESIS OF BIOLOGICALY ACTIVE NATURAL PRODUCTS ACHAETOLIDE, PANAXJAPYNE C, GONIOTHALESDIOL A AND (5R,6S)- newlineACETOXYHEXADECANOLIDE has been divided into four chapters. Chapter I: This chapter describes stereoselective total synthesis of newlineachaetolide by using 2-deoxy-D-ribose involving the grigard reaction, acrocyclization and ring closing metathesis reactions. Chapter II: This chapter deals with first stereoselective total synthesis newlineof panaxjapyne C by using L-Ascorbic acid involving the regioselective epoxide opening and Cadiot-Chodkiewicz cross-coupling reactions. Chapter III: This chapter describes concise stereoselective synthesis newlineof goniothalesdiol A.
Pagination: 132 p.
URI: http://hdl.handle.net/10603/19277
Appears in Departments:Department of Chemistry

Files in This Item:
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01_title.pdfAttached File191.48 kBAdobe PDFView/Open
02_certificate.pdf112.6 kBAdobe PDFView/Open
03_declaration.pdf125.75 kBAdobe PDFView/Open
04_acknowledgement.pdf144.78 kBAdobe PDFView/Open
05_dedication.pdf37.96 kBAdobe PDFView/Open
06_general remarks.pdf122.15 kBAdobe PDFView/Open
07_abbreviations.pdf174.4 kBAdobe PDFView/Open
08_abstract.pdf140.34 kBAdobe PDFView/Open
09_contents.pdf159.09 kBAdobe PDFView/Open
10_chapter 1.pdf332.16 kBAdobe PDFView/Open
11_chapter 2.pdf524.1 kBAdobe PDFView/Open
12_chapter 3.pdf354.37 kBAdobe PDFView/Open
13_chapter 4.pdf374.76 kBAdobe PDFView/Open
14_chapter 5.pdf371.61 kBAdobe PDFView/Open
15_list of publication.pdf196.78 kBAdobe PDFView/Open


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