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dc.contributor.authorXu, Junhui
dc.date.accessioned2016-08-19 14:02:01 (GMT)
dc.date.available2016-08-19 14:02:01 (GMT)
dc.date.issued2016-08-19
dc.date.submitted2016-08-04
dc.identifier.urihttp://hdl.handle.net/10012/10662
dc.description.abstractTwo widely-accepted models (open- and cyclic- transmetalation) are applied to explain the stereochemical outcome of the Stille coupling with organotin compounds containing an sp3 chiral center. However, it is still not possible to predict the stereochemical outcome of this type of Stille coupling before the reaction is conducted. To have a better understanding of the detailed mechanism involved, the Stille couplings of different α-acyloxybenzylstannanes with different acid chlorides were studied in this project.en
dc.language.isoenen
dc.publisherUniversity of Waterlooen
dc.subjectStille couplingen
dc.titleStille Coupling of α-Acyloxybenzylstannanes with Acid Chloridesen
dc.typeMaster Thesisen
dc.pendingfalse
uws-etd.degree.departmentChemistryen
uws-etd.degree.disciplineChemistryen
uws-etd.degree.grantorUniversity of Waterlooen
uws-etd.degreeMaster of Scienceen
uws.contributor.advisorChong, Michael
uws.contributor.affiliation1Faculty of Scienceen
uws.published.cityWaterlooen
uws.published.countryCanadaen
uws.published.provinceOntarioen
uws.typeOfResourceTexten
uws.peerReviewStatusUnrevieweden
uws.scholarLevelGraduateen


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