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Showing 1 to 7 of 7 for “"MIDA boronates"”.

  1. Iterative cross-coupling with MIDA boronates

    … Towards this end, N-methyliminodiacetic acid (MIDA) was discovered to be such a ligand, enabling an approach by which the reactivity of boronic acids is modulated via rehybridization of the boron center. Further, MIDA boronates, which result from the condensation of MIDA with boronic acids, …

    uiuc Repository record for Iterative cross-coupling with MIDA boronates (opens in a new tab)

  2. Slow-release cross-coupling and an advanced method for β-glycosylation: methods stimulated by amphotericin B

    … developed whereby N-methyliminodiacetic acid (MIDA) boronates can be used directly in Suzuki-Miyaura cross-coupling (SMC) reactions, enabling air-stable MIDA boronates to act as surrogates for boronic acids. Additionally, conditions were identified under which MIDA boronates could be slowly …

    uiuc Repository record for Slow-release cross-coupling and an advanced method for β-glycosylation: methods stimulated by amphotericin B (opens in a new tab)

  3. A small molecule synthesizer

    … by the capacity of N-methyliminodiacetic acid (MIDA) to reversibly attenuate the reactivity of a boronic acid. MIDA boronates are generally crystalline free-flowing solids and are stable to bench-top storage. Furthermore, it has been discovered that they are universally amenable to …

    uiuc Repository record for A small molecule synthesizer (opens in a new tab)

  4. Expansion of the iterative cross-coupling synthesis strategy through Csp3 halide cross-coupling, Mida boronate synthesis, and chan-lam couplings

    … We also report a new method for the synthesis of MIDA boronates which are sensitive to current methods. Finally, we report the extension of the entire iterative cross coupling platform to the Chan-Lam coupling to form carbon-heteroatom bonds.

    uiuc Repository record for Expansion of the iterative cross-coupling synthesis strategy through Csp3 halide cross-coupling, Mida boronate synthesis, and chan-lam couplings (opens in a new tab)

  5. Total synthesis and study of the antilipoperoxidant peridinin, synthesis of versatile MIDA boronate building blocks, and a general strategy for the synthesis of polyenes

    … involving the iterative cross-coupling of MIDA boronate containing molecules can be a universal platform for the preparation of small molecules. Guided by this strategy we completed an efficient, flexible, and fully stereocontrolled synthesis of the carotenoid natural product peridinin. …

    uiuc Repository record for Total synthesis and study of the antilipoperoxidant peridinin, synthesis of versatile MIDA boronate building blocks, and a general strategy for the synthesis of polyenes (opens in a new tab)

  6. Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings

    … require conditions which hydrolyze MIDA boronates (aqueous base, high heat, strong base, etc.). In this thesis I describe the development of a second generation iminodiacetic acid ligand for boronic acids which is refractory to hydrolysis and has enabled the first examples of …

    uiuc Repository record for Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings (opens in a new tab)

  7. Stereoselective synthesis and iterative coupling of Csp3 boronates for automating small molecule synthesis

    … synthesis of a wide range of new types of Csp3 boronates. The utility of these Csp3 boronates was demonstrated in the synthesis of a pharmaceutically relevant target using a previously undescribed iterative Csp3-Csp2 coupling. In order to access Csp3-rich cyclic and polycyclic molecules via the …

    uiuc Repository record for Stereoselective synthesis and iterative coupling of Csp3 boronates for automating small molecule synthesis (opens in a new tab)