The versatility of palladium systems: from palladacycles to cyclic peptides and beyond

dc.contributor.committeeMember	Foley, Stephen R
dc.contributor.committeeMember	Sammynaiken, Ramaswami
dc.contributor.committeeMember	Mueller, Jens
dc.creator	Li, Hanxiang 1989-
dc.date.accessioned	2019-10-25T21:16:42Z
dc.date.available	2019-10-25T21:16:42Z
dc.date.created	2015-07
dc.date.issued	2015-08-12
dc.date.submitted	July 2015
dc.date.updated	2019-10-25T21:16:42Z
dc.description.abstract	This work started with the aim to synthesize monomeric ring-opened analogues of the palladacycles [(iminoisoidoline)PdCl(PCy3)] incorporating iminoisoindoline and phosphine ligands, and evaluate their catalytic activities in C-C coupling reactions compared to their monomeric palladacyclic precursors. This project further evolved to investigate cyclic peptides derived from flaxseed oil as alternative ligands in palladium coordination chemistry for applications in C-C coupling reactions. During the course of our studies, we observed that cyclic peptides derived from flaxseed oil had a high affinity for first row transition metals.
dc.format.mimetype	application/pdf
dc.identifier.uri	http://hdl.handle.net/10388/12420
dc.subject	palladacycle, cyclic peptide, suzuki reaction
dc.title	The versatility of palladium systems: from palladacycles to cyclic peptides and beyond
dc.type	Thesis
dc.type.material	text
thesis.degree.department	Chemistry
thesis.degree.discipline	Chemistry
thesis.degree.grantor	University of Saskatchewan
thesis.degree.level	Masters
thesis.degree.name	Master of Science (M.Sc.)

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Name:: Li, Hanxiang_M.Sc._The versatility of palladium systems from palladacycles to cyclic peptides and beyond_July_2015.pdf
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