Molecules containing a chiral S(VI) moiety have found extensive applications in drug design and organic synthesis, despite a lack of diverse asymmetric methods for their creation. Now, a ligand-mediated process has enabled the production of enantioenriched S(VI)–F motifs, providing a foundation for further stereospecific elaborations.
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References
Ilardi, E. A., Vitaku, E. & Njardarson, J. T. J. Med. Chem. 57, 2832–2842 (2014).
Mäder, P. & Kattner, L. J. Med. Chem. 63, 14243–14275 (2020).
Chinthakindi, P. K. et al. Angew. Chem. Int. Ed. 56, 4100–4109 (2017).
Liu, Y. et al. Org. Lett. 23, 3975–3980 (2021).
Dong, J., Krasnova, L., Finn, M. G. & Sharpless, K. B. Angew. Chem. Int. Ed. 53, 9430–9448 (2014).
Sehgelmeble, F. et al. ChemMedChem 7, 396–399 (2012).
Li, S., Wu, P., Moses, J. E. & Sharpless, K. B. Angew. Chem. Int. Ed. 56, 2903–2908 (2017).
Peng, Z. et al. Nat. Chem. https://doi.org/10.1038/s41557-024-01452-w (2024).
Wojaczyńska, E. & Wojaczyński, J. Chem. Rev. 120, 4578–4611 (2020).
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Melvin, P.R. Asymmetric construction of sulfur(VI)–fluorine cores. Nat. Chem. 16, 304–305 (2024). https://doi.org/10.1038/s41557-024-01454-8
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DOI: https://doi.org/10.1038/s41557-024-01454-8