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Showing 1 to 9 of 9 for “"iterative cross-coupling (ICC)"”.

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

    … and other biomolecules, we have pioneered iterative cross coupling (ICC) as an analogous platform for small molecules. Enabled by both a building block based synthesis strategy and a general purification protocol, our group has designed and built a small molecule synthesizer. We have …

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

  2. Iterative cross-coupling with MIDA boronates

    … approach to small molecule making based on the iterative cross-coupling (ICC) of bifunctional haloboronic acid building blocks. Realizing a general ICC approach in the context of small molecule synthesis required the discovery of a ligand with the capacity to attenuate the reactivity of boronic …

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

  3. A small molecule synthesizer

    … C-C bond forming reaction, the Suzuki-Miyaura cross-coupling (SMC) reaction, to assemble off-the-shelf building blocks into many different types of small molecules including organic materials, pharmaceuticals, natural products, and natural product derivatives. Specifically, this automated …

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

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

    … in the construction of the AmB polyene, a new cross-coupling protocol was 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, …

    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)

  5. Part I: synthesis and cross-coupling of the C1-C12 primary organoborane building block of amphotericin B; Part II: site- and stereoretentive cross-coupling of unactivated secondary boronic acids inspired by amphotericin B

    … are readily assembled using only a single cross-coupling reaction repeatedly. Such an iterative cross-coupling (ICC) strategy has been applied in our proposed total synthesis of clinically valuable polyene natural product amphotericin B (AmB). In our retrosynthetic analysis, AmB is …

    uiuc Repository record for Part I: synthesis and cross-coupling of the C1-C12 primary organoborane building block of amphotericin B; Part II: site- and stereoretentive cross-coupling of unactivated secondary boronic acids inspired by amphotericin B (opens in a new tab)

  6. Low-temperature protonation studies of an electron-poor osmium methyl complex, and molecular precursors for the construction of graphene nanostructues with atomically precise edge structures

    … a binomial quintet in the 13C NMR with a coupling constant (127 Hz) almost identical to that of free methane (125 Hz). Kinetic analysis revealed that the enthalpy and entropy of activation for methane loss was ΔH‡ = 14.9 ± 1.5 kcal mol-1 and ΔS‡ = 12.3 ± 8.8 cal mol-1 K-1, respectively, …

    uiuc Repository record for Low-temperature protonation studies of an electron-poor osmium methyl complex, and molecular precursors for the construction of graphene nanostructues with atomically precise edge structures (opens in a new tab)

  7. Less toxic yet still resistance evasive amphotericins and atomistic probing of the amphotericin B ion channel

    … synthesis of AmB was designed grounded in the iterative cross coupling (ICC) strategy for small molecule synthesis. The synthesis was divided into three main phases, building block construction, ICC, and protecting group removal. Advances were made in all three phases. A scalable synthesis of …

    uiuc Repository record for Less toxic yet still resistance evasive amphotericins and atomistic probing of the amphotericin B ion channel (opens in a new tab)

  8. Expansion and automation of iterative cross-coupling: total synthesis of synechoxanthin and development of a small molecule synthesizer

    Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2014-04-15T20:00:36Z Item was in collections: University of Illinois Theses & Dissertations (ID: 1) No. of bitstreams: 1 Sisco_Seiko.pdf: 39731093 bytes, checksum: c5a677f96924a2150cc9bc68dfe0cc54 (MD5)

    uiuc Repository record for Expansion and automation of iterative cross-coupling: total synthesis of synechoxanthin and development of a small molecule synthesizer (opens in a new tab)

  9. Synthesis and function of the conserved motif of mycosamine-containing polyene macrolides

    … platform for small molecule synthesis based on iterative cross-coupling. This synthesis was enabled by the development of a new type of diastereotopic group-selective lactonization and a new directing group for the challenging installation of the mycosamine sugar. This building block may help …

    uiuc Repository record for Synthesis and function of the conserved motif of mycosamine-containing polyene macrolides (opens in a new tab)