Enzymes are capable of controlling the reactivity and selectivity of catalytic mechanisms involving highly reactive intermediates. Now, flavine mononucleotide-dependent ene-reductases have been repurposed as photobiocatalysts for generating and taming unstable N-centred radicals, enabling their application in asymmetric radical C–N couplings.
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References
Zard, S. Z. Chem. Soc. Rev. 37, 1603–1618 (2008).
Kwon, K., Simons, R. T., Nandakumar, M. & Roizen, J. L. Chem. Rev. 122, 2353–2428 (2022).
Zhang, Z. et al. Nat. Catal. https://doi.org/10.1038/s41929-023-00994-5 (2023).
Toogood, H. S. & Scrutton, N. S. ACS Catal. 8, 3532–3549 (2018).
Huang, X. et al. Nature 584, 69–74 (2020).
Biegasiewicz, K. F. et al. Science 364, 1166–1169 (2019).
Page, C. G. et al. J. Am. Chem. Soc. 143, 97–102 (2021).
Reetz, M. T. & Garcia-Borràs, M. J. Am. Chem. Soc. 143, 14939–14950 (2021).
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Garcia-Borràs, M. Photobiocatalysts tame nitrogen-centred radicals. Nat Catal 6, 654–656 (2023). https://doi.org/10.1038/s41929-023-01004-4
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DOI: https://doi.org/10.1038/s41929-023-01004-4