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  1. Free, publicly-accessible full text available September 1, 2024
  2. Booker, S (Ed.)
    Applying enzymatic reactions to produce useful molecules is a central focus of chemical biology. Iron and 2-oxoglutarate (Fe/2OG) enzymes are found in all kingdoms of life and catalyze a broad array of oxidative transformations. Herein, we demonstrate that the activity of an Fe/2OG enzyme can be redirected when changing the targeted carbon hybridization from sp3 to sp2. During leucine 5-hydroxylase catalysis, installation of an olefin group onto the substrate redirects the Fe(IV)−oxo species reactivity from hydroxylation to asymmetric epoxidation. The resulting epoxide subsequently undergoes intramolecular cyclization to form the substituted piperidine, 2S,5S-hydroxypipecolic acid. 
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  3. Free, publicly-accessible full text available October 1, 2024
  4. Free, publicly-accessible full text available August 1, 2024
  5. Free, publicly-accessible full text available July 1, 2024
  6. null (Ed.)