Search Results - "Brenzovich Jr, William E."

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  1. 1

    Gold-Catalyzed Intramolecular Aminoarylation of Alkenes: C----C Bond Formation through Bimolecular Reductive Elimination by Brenzovich, William E. Jr, Benitez, Diego, Lackner, Aaron D, Shunatona, Hunter P, Tkatchouk, Ekaterina, Goddard, William A. III, Toste, F. Dean

    Published in Angewandte Chemie (International ed.) (26-07-2010)
    “…Gold‐ilocks and the 3 mol % catalyst: Bimetallic gold bromides allow the room temperature aminoarylation of unactivated terminal olefins with aryl boronic…”
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    Journal Article
  2. 2

    Gold in Total Synthesis: Alkynes as Carbonyl Surrogates by Brenzovich Jr, William E.

    Published in Angewandte Chemie International Edition (03-09-2012)
    “…Fields of gold: Recent developments in the field of gold catalysis, using an alkyne as a carbonyl equivalent is becoming an important chemical transformation,…”
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  3. 3

    Gold-Catalyzed Oxidative Coupling Reactions with Aryltrimethylsilanes by Brenzovich, William E, Brazeau, Jean-François, Toste, F. Dean

    Published in Organic letters (05-11-2010)
    “…During continuing studies with a novel oxidative gold oxyarylation reaction, arylsilanes were found to be competent coupling partners, providing further…”
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  4. 4

    Gold-Catalyzed Three-Component Coupling: Oxidative Oxyarylation of Alkenes by Melhado, Asa D, Brenzovich, William E, Lackner, Aaron D, Toste, F. Dean

    Published in Journal of the American Chemical Society (07-07-2010)
    “…The three-component coupling of terminal alkenes with arylboronic acids and oxygen nucleophiles is described. The reaction employs a binuclear gold(I) bromide…”
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  5. 5
  6. 6

    Gold-Catalyzed Intramolecular Aminoarylation of Alkenes: CC Bond Formation through Bimolecular Reductive Elimination by Brenzovich Jr, William E., Benitez, Diego, Lackner, Aaron D., Shunatona, Hunter P., Tkatchouk, Ekaterina, Goddard III, William A., Toste, F. Dean

    Published in Angewandte Chemie (26-07-2010)
    “…Zweikernige Goldbromidkomplexe katalysieren die Aminoarylierung nichtaktivierter terminaler Olefine mit Arylboronsäuren und dem Oxidationsmittel Selectfluor…”
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    Journal Article