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Showing 1 to 2 of 2 for “"Miyaura Borylation"”.

  1. Development of New Synthetic Methods for Transition Metal-Catalyzed Organic Reactions and Synthesis of Curcumin-Based Adducts

    … boronic acid/acid esters, which are products of Miyaura borylation, also serve as substrates in transition metal-catalyzed addition reactions. This dual functionality provides an opportunity for a sequential/tandem synthetic process. Based on the hypothesis that the second addition reaction could …

    cuny-grad Repository record for Development of New Synthetic Methods for Transition Metal-Catalyzed Organic Reactions and Synthesis of Curcumin-Based Adducts (opens in a new tab)

  2. I. Reaction mining—a next-generation platform for reaction discovery II. Rapid, anhydrous, homogenous Suzuki-Miyaura cross-coupling of aryl and alkylboronates

    … methods for aryl-aryl and B-alkyl Suzuki-Miyaura cross-coupling of boronic esters and boronates. Chapter 1 describes previous efforts by Sarlah and Shved to accelerate the reaction discovery process with the combination of data science, HTE, and artificial isotope distributions. A workflow …

    uiuc Repository record for I. Reaction mining—a next-generation platform for reaction discovery II. Rapid, anhydrous, homogenous Suzuki-Miyaura cross-coupling of aryl and alkylboronates (opens in a new tab)