- PII
- S3034630425070261-1
- DOI
- 10.7868/S3034630425070261
- Publication type
- Status
- Published
- Authors
- Volume/ Edition
- Volume 61 / Issue number 7
- Pages
- 1054-1058
- Abstract
- Chemodivergent synthesis of 2-(phenylsulfonyl)pyridine and pyridin-2-yl benzenesulfinate was performed from 2-iodopyridine and sodium phenylsulfinate using Ni/photoredox-catalysis under visible light irradiation (450 nm, 30 W). It was shown that the nature of the photocatalyst determines the formation of C-S or C-O product.
- Keywords
- фотокатализ никелевый катализ двойной фотокатализ сульфоны диарилсульфинаты
- Date of publication
- 01.07.2025
- Year of publication
- 2025
- Number of purchasers
- 0
- Views
- 25
References
- 1. Ivachtchenko A., Golovina E., Kadieva M. et al. Bioorg. Med. Chem., 2013, 21, 4614–4627. https://doi.org/10.1016/j.bmc.2013.05.040
- 2. Ma Y., Liu R., Gong X. et al. J. Agric. Food Chem., 2006, 54, 7724−7728. https://doi.org/10.1021/jf0609328
- 3. Liang S., Hofman K., Friedrich M. et al. ChemSusChem, 2021, 14, 4878–4902. https://doi.org/10.1002/cssc.202101635
- 4. Choudary B.M., Chowdari N.S., Kantam M.L. J. Chem. Soc., Perkin Trans., 2000, 1, 2689–2693. https://doi.org/10.1039/b002931i
- 5. Beletskaya I.P., Ananikov V.P. Chem. Rev., 2022, 122, 16110–16293. https://doi.org/10.1021/acs.chemrev.1c00836
- 6. Cabrera-Afonso M.J., Lu Z.-P., Kelly C.B. et al. Chem. Sci., 2018, 9, 3186–3191. https://doi.org/10.1039/C7SC05402E
- 7. Chawla R., Yadav L.D.S. Org. Biomol. Chem., 2019, 17, 4761–4766. https://doi.org/10.1039/C9OB00864K
- 8. Jiang S., Zhang Z.-T., Young D.J. et al. Org. Chem. Front., 2022, 9, 1437–1444. https://doi.org/10.1039/d1qo01850g
- 9. Kim M., You E., Park S., Hong S. Chem. Sci., 2021, 12, 6629–6637. https://doi.org/10.1039/D1SC00776A
- 10. Liu N.-W., Hofman K., Herbert A., Manolikakes G. Org. Lett., 2018, 20, 760–763. https://doi.org/10.1021/acs.orglett.7b03896
- 11. Yue H., Zhu C., Rueping M. Angew. Chem. Int. Ed., 2018, 57, 1371–1375. https://doi.org/10.1002/anie.201711104
- 12. Ionova V.A., Abel A.S., Averin A.D., Beletskaya I.P. Adv. Syn. Catal., 2024, 366, 3173–3180. https://doi.org/10.1002/adsc.202400350
- 13. Zhu D.-L., Li J., Young D.J. et al. Tetrahedron, 2025, 184, 134733. https://doi.org/10.1016/j.tet.2025.134733
- 14. Chan A.Y., Perry I.B., Bissonnette N.B. et al. Chem. Rev., 2022, 122, 1485–1542. https://doi.org/10.1021/acs.chemrev.1c00383
- 15. Baidya M., Kobayashi S., Mayr H. J. Am. Chem. Soc. 2010, 132, 4796–4805. https://doi.org/10.1021/ja9102056
- 16. Cacchi S., Fabrizi G., Goggiamani A. et al. J. Org. Chem., 2004, 69, 5608–5614. https://doi.org/10.1021/jo0493469
- 17. Ionova V.A., Dmitrieva A.V., Abel A.S. et al. Dalton Trans., 2024, 53, 17021–17035. https://doi.org/10.1039/D4DT02067G
- 18. Garreau M., Le Vaillant F., Waser J. Angew. Chem. Int. Ed., 2019, 58, 8182–8186. https://doi.org/10.1002/anie.201901922