Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/19277
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dc.coverage.spatialChemistryen_US
dc.date.accessioned2014-06-13T09:26:40Z-
dc.date.available2014-06-13T09:26:40Z-
dc.date.issued2014-06-13-
dc.identifier.urihttp://hdl.handle.net/10603/19277-
dc.description.abstractThe 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.en_US
dc.format.extent132 p.en_US
dc.languageEnglishen_US
dc.relation-en_US
dc.rightsuniversityen_US
dc.titleStereoselective Total Synthesis of Biologically Active Natural Products Achaetolide Panaxjapyne C, Goniothalesdiol A and ( 5 R, 6 S)- Acetoxyhexadecanolideen_US
dc.title.alternative-en_US
dc.creator.researcherThakur, Pallavien_US
dc.subject.keywordAcetoxyhexadecanolideen_US
dc.subject.keywordActiveen_US
dc.subject.keywordBiologicallyen_US
dc.subject.keywordGoniothalesdioen_US
dc.subject.keywordStereoselectiveen_US
dc.subject.keywordSynthesisen_US
dc.description.noteReferences included in the chaptersen_US
dc.contributor.guideBandichhor, Rakeshwaren_US
dc.contributor.guideMukkanti, Ken_US
dc.publisher.placeKukatpallyen_US
dc.publisher.universityJawaharlal Nehru Technological University, Hyderabaden_US
dc.publisher.institutionDepartment of Chemistryen_US
dc.date.registeredn.d.en_US
dc.date.completed2013en_US
dc.date.awardedn.d.en_US
dc.format.dimensions-en_US
dc.format.accompanyingmaterialNoneen_US
dc.type.degreePh.D.en_US
dc.source.inflibnetINFLIBNETen_US
Appears in Departments:Department of Chemistry

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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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