Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp01jh343v68g
 Title: Nickel Catalysis: Asymmetric Arylation of Quinolinium Ions and the Development of an Air-Stable Precatalyst Authors: Shields, Jason Daniel Advisors: Doyle, Abigail G Contributors: Chemistry Department Keywords: AsymmetricCatalysisIminiumNickelPrecatalystStable Subjects: Organic chemistry Issue Date: 2015 Publisher: Princeton, NJ : Princeton University Abstract: Although both palladium and nickel were reported to catalyze cross-coupling reactions some four decades ago, palladium became the catalyst of choice for most chemists, due in part to the greater air stability of Pd(0) relative to Ni(0). Nevertheless, nickel is a desirable catalyst for two reasons. First, nickel is three orders of magnitude less expensive than palladium. Second, nickel offers reactivity distinct from palladium due in part to the difference in electronegativity between the metals—for example, palladium is more likely to mediate C–H activation, while nickel more readily reacts with pi-systems, effecting cyclization reactions of olefins. In this dissertation, we describe two projects that leverage these advantages. First, we discuss the application of a nickel-iminium activation mode to an enantioselective crosscoupling reaction between arylboroxines and quinolinium ions. This reaction allows access to enantioenriched 2-aryl-1,2-dihydroquinolines with unprecedented stereoselectivity. A necessary step in the optimization of this reaction was the use of an unusual precatalyst, [(methallyl)NiCl]2, instead of the more commonly used Ni(cod)2. Second, we detail the development of [(TMEDA)Ni(o-tolyl)Cl], a modular, airstable nickel precatalyst. We believe this nickel source is a useful alternative to other nickel precatalysts reported in the literature. Due to the lability of TMEDA, this complex can be used in conjunction with mono- and bidentate phosphines, diimines, and NHC ligands, which is crucial to its success as a precatalyst in Suzuki–Miyaura, Buchwald–Hartwig, cyclization, and oxidative coupling reactions. URI: http://arks.princeton.edu/ark:/88435/dsp01jh343v68g Alternate format: The Mudd Manuscript Library retains one bound copy of each dissertation. Search for these copies in the library's main catalog: http://catalog.princeton.edu/ Type of Material: Academic dissertations (Ph.D.) Language: en Appears in Collections: Chemistry

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