1. Shodhganga@INFLIBNET
  2. Thapar Institute of Engineering and Technology
  3. School of Chemistry and Biochemistry
Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/340111
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DC FieldValueLanguage
dc.coverage.spatial
dc.date.accessioned2021-09-14T03:48:10Z-
dc.date.available2021-09-14T03:48:10Z-
dc.identifier.urihttp://hdl.handle.net/10603/340111-
dc.description.abstractThe thesis entitled Synthesis of Natural Fragrance, Pheromone and Bioactive Compounds is divided into four different chapters. The present thesis comprises the concise and enantioselective approaches towards asymmetric syntheses of (-)-trans-aerangis lactone, (S)-ethyl 4-methyloctanoate and (-)-clavaminol A and deacetyl (+)-clavaminol H. The key steps involved for asymmetric synthesis are Sharpless Asymmetric Dihydroxylation (AD)and organocatalyzed aldol reactions. newline
dc.format.extent80p.
dc.languageEnglish
dc.relation
dc.rightsuniversity
dc.titleSynthesis of Natural Fragrance Pheromone and Bioactive Compounds
dc.title.alternative
dc.creator.researcherPandey, Rachana
dc.subject.keywordMacMillan Cross Aldol Reaction
dc.subject.keywordPheromone and Bioactive Compounds
dc.subject.keywordSynthesis of Natural Fragrance
dc.description.note
dc.contributor.guidePrakash, Ranjana
dc.publisher.placePatiala
dc.publisher.universityThapar Institute of Engineering and Technology
dc.publisher.institutionSchool of Chemistry and Biochemistry
dc.date.registered
dc.date.completed2019
dc.date.awarded
dc.format.dimensions
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:School of Chemistry and Biochemistry

Files in This Item:
File Description SizeFormat 
01_title.pdfAttached File110.35 kBAdobe PDFView/Open
02_certificate.pdf1.64 MBAdobe PDFView/Open
03_candidates declaration.pdf1.55 MBAdobe PDFView/Open
04_dedication.pdf121.73 kBAdobe PDFView/Open
05_acknowledgements.pdf348.72 kBAdobe PDFView/Open
06_index.pdf444.19 kBAdobe PDFView/Open
07_abbreviations.pdf474.84 kBAdobe PDFView/Open
08_general remarks.pdf565.35 kBAdobe PDFView/Open
09_abstract.pdf848.76 kBAdobe PDFView/Open
10_list of publications.pdf472.6 kBAdobe PDFView/Open
11_chapter 1.pdf1.14 MBAdobe PDFView/Open
12_chapter 2.pdf2.3 MBAdobe PDFView/Open
13_chapter 3.pdf1.58 MBAdobe PDFView/Open
14_chapter 4.pdf3.01 MBAdobe PDFView/Open
15_references.pdf2.16 MBAdobe PDFView/Open
80_recommendation.pdf3.14 MBAdobe PDFView/Open
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