Please use this identifier to cite or link to this item: 192.168.6.56/handle/123456789/75903
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dc.contributor.advisorLautens, Mark-
dc.contributor.authorA. Petrone, David-
dc.date.accessioned2019-07-11T06:07:12Z-
dc.date.available2019-07-11T06:07:12Z-
dc.date.issued2018-
dc.identifier.isbn978-3-319-77507-4-
dc.identifier.urihttp://10.6.20.12:80/handle/123456789/75903-
dc.descriptionMy Ph.D. studies in the research group of Prof. Mark Lautens at the University of Toronto focused on using palladium catalysts modified by bulky phosphine ligands to promote the highly stereoselective formation of several classes of heterocycles. My initial venture into this research topic was initiated during study aimed to examine the stereoselective synthesis of chromans and isochromans via the cyclization strategy which has been designated “arylohalogenation” throughout this thesis. This project was initiated by a talented post-doctoral fellow named Dr. Hasnain Malik who mentored me during my studies. The knowledge gained throughout this project led to our group’s more general interest in the stereoselective syntheses of other classes of halogenated heterocycles-
dc.languageenen
dc.languageenen
dc.language.isoenen_US
dc.publisherSpringer International Publishing AGen_US
dc.subjectHeterocycleen_US
dc.titleStereoselective Heterocycle Synthesis via Alkene Difunctionalizationen_US
dc.typeBooken_US
Appears in Collections:Chemistry

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