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Creators/Authors contains: "Schomaker, Jennifer M"

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  1. ; ; ; ; ; (, Chem Catalysis)
    Free, publicly-accessible full text available May 1, 2026
  2. ; ; (, Accounts of Chemical Research)
    Free, publicly-accessible full text available January 21, 2026
  3. ; ; ; ; ; (, Journal of the American Chemical Society)
    Free, publicly-accessible full text available February 12, 2026
  4. ; ; ; (, Chemical Science)
    Rational ligand design in a silver catalyst enables highly selective amination of electron-deficient heterobenzylic C–H bondsvianitrene transfer, with scaffold rigidity crucial for unlocking this elusive reactivity in heteroaromatic compounds. 
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    Free, publicly-accessible full text available January 1, 2026
  5. ; ; ; ; ; ; ; ; (, ACS Catalysis)
    Free, publicly-accessible full text available February 18, 2026
  6. ; ; ; ; ; ; ; (, Journal of the American Chemical Society)
    Full Text Available 
  7. ; ; ; ; (, The Journal of Organic Chemistry)
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  8. ; ; (, Organic Letters)
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  9. ; ; ; (, ChemSusChem)
    Abstract Transition metal‐catalyzed, non‐enzymatic nitrene transfer (NT) reactions to selectively transform C−H and C=C bonds to new C−N bonds are a powerful strategy to streamline the preparation of valuable amine building blocks. However, many catalysts for these reactions use environmentally unfriendly solvents that include dichloromethane, chloroform, 1,2‐dichloroethane and benzene. We developed a high‐throughput experimentation (HTE) protocol for heterogeneous NT reaction mixtures to enable rapid screening of a broad range of solvents for this chemistry. Coupled with the American Chemical Society Pharmaceutical Roundtable (ACSPR) solvent tool, we identified several attractive replacements for chlorinated solvents. Selected catalysts for NT were compared and contrasted using our HTE protocol, including silver supported byN‐dentate ligands, dinuclear Rh complexes and Fe/Mn phthalocyanine catalysts. 
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  10. ; ; ; ; ; ; (, Chemical Communications)
    Transition metal-catalyzed asymmetric nitrene transfer is a powerful method to generate enantioenriched amines found in natural products and bioactive molecules. 
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