Synthesis and Competitive of Reaction Rate Experiments for a Series of Ni(II) Complexed Nucleophilic Glycine Equivalents

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dc.contributor.authorEllis, Trevor
dc.date.accessioned2026-02-23T20:36:32Z
dc.date.available2026-02-23T20:36:32Z
dc.date.issued3/8/2019
dc.description.abstractThe preparation of two Ni(II) complexed Schiff’s Base derived nucleophilic glycine equivalents will be described including the synthesis of the required ligands and 2-aminobenzophenones. Additionally, these complexes will be evaluated regarding their utility for the preparation of non-proteinogenic ?-amino acids. Two methods of homologation, alkyl halide alkylation and Michael Addition Reactions, will be utilized to evaluate the reactivity of these Ni(II) complexed glycine equivalents compared to previous generations that have been introduced through competitive reaction approaches.
dc.description.departmentSouthwestern Oklahoma State University
dc.identifier.otherMathematics and Science.Chemistry.41
dc.identifier.urihttps://shareok.org//handle/11244/342114
dc.relation.ispartofseriesMathematics and Science
dc.subject.keywordsChemistry
dc.titleSynthesis and Competitive of Reaction Rate Experiments for a Series of Ni(II) Complexed Nucleophilic Glycine Equivalents
dc.typeAbstract

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2019 Oklahoma Research Day