Heteroaryl Isoflavone compounds as aromatase inhibitors: Diketone Reaction Exploration

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dc.contributor.authorRosen, Alex
dc.date.accessioned2021-08-16T13:17:16Z
dc.date.available2021-08-16T13:17:16Z
dc.date.created2020
dc.description2020 Celebration of Student Research and Creativity presentationen_US
dc.description.abstractThe overall goal of the research conducted was to synthesize a potential aromatase inhibitor through a heteroarylation reaction. Previously, a diketone compound was synthesized through the course of our normal research. After a synthetic route was created and confirmed, work began to synthesize a library of diketone compounds. Products were synthesized through a two-step method, in which the compound was synthesized through our base reaction. Once the compound was confirmed by NMR, the second step involved the formation of the diketone under microwave irradiation. A library of successful products and their pure yields is reported in this poster.en_US
dc.description.urihttps://youtu.be/2zhh5xAc4K0en_US
dc.identifier.urihttp://hdl.handle.net/11216/3914
dc.language.isoen_USen_US
dc.publisherNorthern Kentucky Universityen_US
dc.relation.ispartofseriesCelebration of Student Research and Creativity;2020
dc.subjectKetonesen_US
dc.subjectIsoflavonesen_US
dc.subjectAromataseen_US
dc.titleHeteroaryl Isoflavone compounds as aromatase inhibitors: Diketone Reaction Explorationen_US
dc.typePresentationen_US

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Student Research and Creativity