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Showing 1 to 13 of 13 for “"iridium catalyzed"”.

  1. Iridium-Catalyzed Enantioselective Allylation of Alkenyl Boronates

    … Additionally, select examples of iridium-catalyzed nucleophilic substitution reactions will be examined. The second chapter describes the reaction of alkenyl boronates with allylic carbonates to generate tertiary bis-homoallyl boronic esters with high enantioselectivity and …

    utswmed Repository record for Iridium-Catalyzed Enantioselective Allylation of Alkenyl Boronates (opens in a new tab)

  2. Mechanistic studies on iridium catalyzed allylic substitution

    Mechanistic studies on iridium catalyzed allylic substitution reactions catalyzed by iridium phosphoramidite complexes revealed that the active catalyst is generated through a base assisted cyclometalation of the phosphoramidite to form five-membered iridacycle. A mechanism for the reaction was …

    uiuc Repository record for Mechanistic studies on iridium catalyzed allylic substitution (opens in a new tab)

  3. Bipyridine Ligands for use in Polymer-Supported Iridium Catalyzed C-H Borylation

    … such as 4, 4’-tert-butyl-bipyrine with an iridium precatalyst afford a highly efficient C-H borylation, but studies of polymer-supported bipyridine ligands have not been extensively researched. With an aim to exploring this approach to allow recycling of the expensive iridium catalysts …

    durham Repository record for Bipyridine Ligands for use in Polymer-Supported Iridium Catalyzed C-H Borylation (opens in a new tab)

  4. Iridium-catalyzed borylation of aromatic and aliphatic C-H bonds: methodology and mechanism

    … conduct the one-pot, meta cyanation of arenes by iridium-catalyzed C-H borylation and copper-mediated cyanation of the resulting arylboronate esters is described in Chapter 2. This process relies on a previously unknown method to conduct the cyanation of arylboronic esters, and conditions for this …

    uiuc Repository record for Iridium-catalyzed borylation of aromatic and aliphatic C-H bonds: methodology and mechanism (opens in a new tab)

  5. A hydrogen bonding ortho-directing effect for the iridium catalyzed borylation of NH(t-BOC) aromatics

    … and others act as steric obstacles for the iridium catalyst to avoid. This avoidance of appending groups can be reversed into a directed borylation with monophosphine ligands. Alternatively, the SiMe2H group elicits an ortho-directing effect via oxidative addition to the metal center. …

    msu Repository record for A hydrogen bonding ortho-directing effect for the iridium catalyzed borylation of NH(t-BOC) aromatics (opens in a new tab)

  6. Investigating Rings: From Iridium-Catalyzed [4+2] Cycloadditions of Alkynyl Halides to Ring Openings of Cyclopropanated Oxabenzonorbornadiene

    This thesis describes two unrelated projects. Iridium-catalyzed intramolecular [4+2] cycloadditions of alkynyl halides were investigated, and the catalyst conditions were optimized for ligand, solvent, and temperature. Several substrates successfully underwent cycloaddition under the optimized …

    guelph Repository record for Investigating Rings: From Iridium-Catalyzed [4+2] Cycloadditions of Alkynyl Halides to Ring Openings of Cyclopropanated Oxabenzonorbornadiene (opens in a new tab)

  7. Sequential Enantioselective Iridium-Catalyzed Allylic Alkylation/Cope Rearrangement for the Construction of Acyclic γ-Tertiary or Quaternary Stereocenters

    … In this way, enantioselective transition metal-catalyzed γ-allylic alkylation reactions have attracted increasing attention, albeit they are typically restricted to cyclic nucleophiles. A direct strategy to construct acyclic γ-allylated carbonyl derivates is underdeveloped due to the challenging …

    queens Repository record for Sequential Enantioselective Iridium-Catalyzed Allylic Alkylation/Cope Rearrangement for the Construction of Acyclic γ-Tertiary or Quaternary Stereocenters (opens in a new tab)

  8. New methodologies and approaches to reaction discovery in transition metal catalysis

    … synthetic methods have been developed based upon iridium-catalyzed borylation of aromatic and heteroaromatic C-H bonds. A general, one-pot method for alkylation of arenes with the site-selectivity controlled by steric effects as opposed to electronic effects via Ir-catalyzed C-H borylation …

    uiuc Repository record for New methodologies and approaches to reaction discovery in transition metal catalysis (opens in a new tab)

  9. Diversification of 4-Alkylpyridines: Mining for Reactivity with Alkylidene Dihydropyridines

    … demonstrated the utility of ADHPs in palladium-catalyzed reactions. However, the fundamental reactivity of ADHPs remains largely unexplored, with only scattered reports in the literature. We seek to further explore the reactivity of these electron-rich intermediates in different contexts, as new …

    york Repository record for Diversification of 4-Alkylpyridines: Mining for Reactivity with Alkylidene Dihydropyridines (opens in a new tab)

  10. Carbon-carbon bond formation methods for the preparation of shape-persistent architectures

    … and utilization of three methodologies: iridium-catalyzed arene C-H borylation; zinc- mediated alkynylations; and Lewis acid promoted Mo nitride-alkyne metathesis, are presented as improvements for the preparation of carbon-rich architectures. In addition, X-ray crystallographic analysis …

    uiuc Repository record for Carbon-carbon bond formation methods for the preparation of shape-persistent architectures (opens in a new tab)

  11. Synthesis of Amphibian Alkaloids and Development of Acetaminophen Analogues

    … ee and 86% ee, respectively. An enantioselective iridium-catalyzed N-heterocyclization reaction with either (R)- or (S)-1-phenylethylamine and 1-(5-methoxypyridin-3-yl)-1, 5-pentanediol was employed to generate the 2-(pyridin-3-yl)-piperidine ring system in 69-72% yield. A cis-2, 5-disubstitued …

    uno Repository record for Synthesis of Amphibian Alkaloids and Development of Acetaminophen Analogues (opens in a new tab)

  12. Novel Enantiopure ß-Amino Alcohols and ß-Amino Thiols in Asymmetric Catalysis

    … then applied as ligands in the ruthenium- and iridium-catalyzed transfer hydrogenation of prochiral ketones. They were shown to be active catalysts, affording in some cases >90% conversion already after 15 minutes, and in all cases ees higher than 80%.

    aachen Repository record for Novel Enantiopure ß-Amino Alcohols and ß-Amino Thiols in Asymmetric Catalysis (opens in a new tab)

  13. Total Synthesis of the Unique Pederin Family Member Psymberin & Chemical Studies Toward Saliniketal Family Members: Saliniketal a, Salinisporamycin and Rifsaliniketal

    … and the synthetic highlights were including the Iridium-catalyzed bis-allylation of 2,2-imethylpropane-1,3-diol, and a stepwise Sonogashira coupling/cycloisomerization/reduction sequence to construct the dihydroisocoumarin unit. The total synthesis of psymberin and its analogs would provide …

    utswmed Repository record for Total Synthesis of the Unique Pederin Family Member Psymberin & Chemical Studies Toward Saliniketal Family Members: Saliniketal a, Salinisporamycin and Rifsaliniketal (opens in a new tab)