Enantioselective Aziridinium/Fluoronium Ion Formation Using Lewis Base Catalysis

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dc.contributor.advisorDr. Brett Hemric
dc.contributor.authorGarcia, Thalia
dc.date.accessioned2023-04-20T15:01:59Z
dc.date.available2023-04-20T15:01:59Z
dc.date.issued2023-04-19
dc.descriptionRecommended citation: Garcia, Thalia. “Enantioselective Aziridinium/Fluoronium Ion Formation Using Lewis Base Catalysis.” Honors Program, The University of Tampa, 2023. https://doi.org/10.48497/FD3B-5182.en_US
dc.description.abstractEfforts toward establishing the concept of enantioselective Lewis base catalysis with nitrogen sources is reported. This project seeks to address challenges in alkene amination chemistry by developing diastereo-, enantio- and regioselective addition of nitrogen to alkenes using Lewis base catalysis to provide advances to the stereoselectivity shortcomings of current approaches. Furthermore, due to the unprecedented exploration of using non-hypervalent Row 2 electrophiles in Lewis base catalysis, this research offers the potential for groundbreaking innovation in this field. This report details the investigation of different nitrogen substrates, Lewis base catalysis, and nucleophiles in varied alkene systems to determine the potential synergy in doing an alkene amination through Lewis base catalysis.en_US
dc.identifier.citationGarcia, Thalia. “Enantioselective Aziridinium/Fluoronium Ion Formation Using Lewis Base Catalysis.” Honors Program, The University of Tampa, 2023. https://doi.org/10.48497/FD3B-5182.
dc.identifier.doihttps://doi.org/10.48497/FD3B-5182
dc.identifier.urihttp://hdl.handle.net/20.500.11868/3914
dc.language.isoen_USen_US
dc.publisherHonors Program, The University of Tampaen_US
dc.subjectNitrogenen_US
dc.subjectLewis base catalysisen_US
dc.subjectAlkene difunctionalizationen_US
dc.titleEnantioselective Aziridinium/Fluoronium Ion Formation Using Lewis Base Catalysisen_US
dc.typeThesisen_US

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