Search Results - "Moghadam, Farbod A."

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  1. 1

    Sustainable Palladium-Catalyzed Tsuji–Trost Reactions Enabled by Aqueous Micellar Catalysis by Lee, Nicholas R, Moghadam, Farbod A, Braga, Felipe C, Lippincott, Daniel J, Zhu, Bingchun, Gallou, Fabrice, Lipshutz, Bruce H

    Published in Organic letters (02-07-2020)
    “…Palladium-catalyzed allylic substitution, or “Tsuji–Trost” reactions, can be run under micellar catalysis conditions featuring not only chemistry in water but…”
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    Journal Article
  2. 2

    Formation of All-Carbon Quaternary Centers via Enantioselective Pd-Catalyzed α‑Vinylation of γ‑Lactams by Moghadam, Farbod A., Barbor, Jay P., Chan, Melinda, Jette, Carina, Sakurai, Shunya, Stoltz, Brian M.

    Published in Organic letters (13-09-2024)
    “…Herein, we report an enantioselective vinylation of α-substituted γ-lactams that forges quaternary centers in up to 59% yield with 94% ee. The use of…”
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    Journal Article
  3. 3

    Ir-Catalyzed Asymmetric Allylic Alkylation of Dialkyl Malonates Enabling the Construction of Enantioenriched All-Carbon Quaternary Centers by Moghadam, Farbod A., Hicks, Elliot F., Sercel, Zachary P., Cusumano, Alexander Q., Bartberger, Michael D., Stoltz, Brian M.

    Published in Journal of the American Chemical Society (11-05-2022)
    “…An enantioselective iridium-catalyzed allylic alkylation of malonates with trisubstituted allylic electrophiles to form all-carbon quaternary stereocenters is…”
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    Journal Article
  4. 4

    What is a cross-coupling? An argument for a universal definition by Reimann, Christopher E., Kim, Kelly E., Rand, Alexander W., Moghadam, Farbod A., Stoltz, Brian M.

    Published in Tetrahedron (09-01-2023)
    “…Despite amazing advances in cross-coupling technologies over the past several decades, there is not a consistent definition of what a cross-coupling reaction…”
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    Journal Article
  5. 5

    Coolade. A Low‐Foaming Surfactant for Organic Synthesis in Water by Lee, Nicholas R., Cortes‐Clerget, Margery, Wood, Alex B., Lippincott, Daniel J., Pang, Haobo, Moghadam, Farbod A., Gallou, Fabrice, Lipshutz, Bruce H.

    Published in ChemSusChem (05-07-2019)
    “…Several types of reduction reactions in organic synthesis are performed under aqueous micellar‐catalysis conditions (in water at ambient temperature), which…”
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    Journal Article