Direct Alkenylation of Vinyl Halides: Reaction Discovery through High-Throughput Experimentation

dc.contributor.authorCruise, Odhran
dc.date.accessioned2023-03-18T17:35:37Z
dc.date.available2023-03-18T17:35:37Z
dc.date.copyright2023en_US
dc.date.issued2023-03-18
dc.description.abstractA broadly applicable method for carbon-carbon bond formation via carbon-hydrogen bond activation has been developed using palladium catalysis. This transformation couples aromatic heterocycles and vinyl halides in a direct alkenylation reaction. High-throughput experimentation techniques were used to conduct multivariate testing methods to rapidly assess and optimize chemical systems across a broad range of substrates. Compared to traditional methods, high-throughput experimentation allows researchers to run arrays of reactions in parallel reducing timelines from months to days. High-throughput methods were throughout the entire process, from reaction discovery to preparative scale optimization, enabling faster drug discovery timelines in the pharmaceutical industry. The products resulting from the transformation developed are biologically active and contain synthetic handles for further functionalization. This enables researchers to expand the potential scope of products for applications in the pharmaceutical industry.en_US
dc.description.reviewstatusRevieweden_US
dc.description.scholarlevelUndergraduateen_US
dc.description.sponsorshipJamie Cassels Undergraduate Research Awards (JCURA)en_US
dc.identifier.urihttp://hdl.handle.net/1828/14881
dc.language.isoenen_US
dc.subjecthigh-throughput experimentationen_US
dc.subjectindustrial collaborationen_US
dc.subjectchemistryen_US
dc.subjectScienceen_US
dc.titleDirect Alkenylation of Vinyl Halides: Reaction Discovery through High-Throughput Experimentationen_US
dc.typePosteren_US

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