Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/423751
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dc.date.accessioned2022-12-09T10:32:50Z-
dc.date.available2022-12-09T10:32:50Z-
dc.identifier.urihttp://hdl.handle.net/10603/423751-
dc.description.abstractChapter1:Natural products have evolved over millions of years, possesses multi-dimensional chemical structures; which results in diversity in their biological activities and drug-like properties. Natural products will undergo continual use towards meeting the urgent need to develop effective drugs, and in turn play a noteworthy part in the discovery of therapeutic agents for curing human diseases. 1 Among the various techniques used to create analogues and derivatives of natural products, asymmetric synthesis by applying chiral auxiliary and new methodologies consisting of fewer steps and lesser cost, are of great significance. Catalytic asymmetric reactions provide a practical entry into the chiral world due to their economical use of asymmetry inducing agents. The osmium tetroxide-catalyzed Sharpless asymmetric dihydroxylation (AD) of olefins, embedding two hydroxyl groups in a hydrocarbon framework is perhaps one of the well-grounded and selective transformations in organic chemistry. Chapter2:The orexins (hypocretins)11 functions as neurotransmitter and widely participate in sleep regulations.12 This correlation demonstrated the use of Orexin receptors for the cure of sleep illness in place of sedative hypnotics that may cause unwanted side effects. Campeau and coworkers13a discovered a structurally distinct, dual Orexin Receptor Antagonists (DORA) named MK-6096 (Figure 1) that was under evaluation to be used as a potent drug for the treatment of insomnia. MK-6096 15, consist of trans-2,5 disubstituted piperidinyl core 16, a biaryl acid and fluoropyridine fragment. Chapter3:In the early 1990 s, Ksander and co-workers developed an active pharmaceutical compound Sacubitril (AUH-377) 31 which is a pro drug neprilysin inhibitor. 16a Combinations of Sacubitril 31 with the angiotensin II receptor-blocker Valsartan 32 by co-crystallization are known as supramolecular complex LCZ696 which was developed by Novartis for the treatment of heart failure (HF).
dc.format.extent119p.
dc.languageEnglish
dc.relation
dc.rightsuniversity
dc.titleEnantioselective Total Synthesis of Bioactive Compounds Employing Transition Metal Based Chiral Ligands and Organocatalysis
dc.title.alternative
dc.creator.researcherKaur, Amanpreet
dc.subject.keywordBioactive compounds
dc.subject.keywordChemistry
dc.subject.keywordChemistry Multidisciplinary
dc.subject.keywordOrganocatalysis
dc.subject.keywordPhysical Sciences
dc.description.note
dc.contributor.guidePandey, Satyendra Kumar and Prakash, Ranjana
dc.publisher.placePatiala
dc.publisher.universityThapar Institute of Engineering and Technology
dc.publisher.institutionSchool of Chemistry and Biochemistry
dc.date.registered
dc.date.completed2022
dc.date.awarded2022
dc.format.dimensions
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:School of Chemistry and Biochemistry

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01_title.pdfAttached File191.04 kBAdobe PDFView/Open
02_prelim pages.pdf1.95 MBAdobe PDFView/Open
03_content.pdf246.63 kBAdobe PDFView/Open
04_abstract.pdf1.07 MBAdobe PDFView/Open
05_chapter 1.pdf1.02 MBAdobe PDFView/Open
06_chapter 2.pdf2.53 MBAdobe PDFView/Open
07_chapter 3.pdf3.45 MBAdobe PDFView/Open
08_chapter 4.pdf3.78 MBAdobe PDFView/Open
09_chapter 5.pdf644.44 kBAdobe PDFView/Open
10_annexures.pdf2.36 MBAdobe PDFView/Open
80_recommendation.pdf660.85 kBAdobe PDFView/Open


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