Библиография

1. 1. Inoue M., Sumii Y., Shibata N., ACS Omega, 2020, 5, 10633–10640. https://doi.org/10.1021/acsomega.0c00830
2. 2. Ogawa Y., Tokunaga E., Kobayashi O., Hirai K., Shibata N., iScience, 2020, 23, 101467. https://doi.org/10.1016/j.isci.2020.101467
3. 3. Nenajdenko V., Fluorine in Heterocyclic Chemistry. Springer International Publishing: Cham, Switzerland, 2014; Vol. 1 and 2.
4. 4. Han J., Remete A.M., Dobson L.S., Kiss L., Izawa K., Moriwaki H., Soloshonok V.A., O'Hagan D., J. Fluorine Chem., 2020, 239, 109639. https://doi.org/10.1016/j.jfluchem.2020.109639
5. 5. Johnson B.M., Shu Y.-Z., Zhuo X., Meanwell N.A., J. Med. Chem., 2020, 63, 6315–6386. https://doi.org/10.1021/acs.jmedchem.9b01877
6. 6. Pankov R.O., Prima D.O., Ananikov V.P., Coord. Chem. Rev., 2024, 516, 215897. https://doi.org/10.1016/j.ccr.2024.215897
7. 7. Schmidt A., Dreger A., Curr. Org. Chem., 2011, 15, 1423–1463. https://doi.org/10.2174/138527211795378263
8. 8. Giornal F., Pazenok S., Rodefeld L., Lui N., Vors J.-P., Leroux F.R., J. Fluorine Chem., 2013, 152, 2–11. https://doi.org/10.1016/j.jfluchem.2012.11.008
9. 9. Mykhailiuk P.K., Chem. Rev., 2021, 121, 1670–1715. https://doi.org/10.1021/acs.chemrev.0c01015
10. 10. Penning T.D., Talley J.J., Bertenshaw S.R., Carter J.S., Collins P.W., Docter S., Graneto M.J., Lee L.F., Malecha J.W., Miyashiro J.M., Rogers R.S., Rogier D.J., Yu S.S., Anderson G.D., Burton E.G., Cogburn J.N., Gregory S.A., Koboldt C.M., Per-kins W.E., Seibert K., Veenhuizen A.W., Zhang Y.Y., Isakson P.C., J. Med. Chem., 1997, 40, 1347–1365. https://doi.org/10.1021/jm960803q
11. 11. Duarte Hospital C., Tête A., Debizet K., Imler J., Tomkiewicz-Raulet C., Blanc E.B., Barouki R., Coumoul X., Bortoli S., Environ. Int., 2023, 180, 108219. https://doi.org/10.1016/j.envint.2023.108219
12. 12. Dias H.V.R., Lovely C.J., Chem. Rev., 2008, 108, 3223–3238. https://doi.org/10.1021/cr078362d
13. 13. Mykhailiuk P.K., Ishchenko A.Y., Stepanenko V., Cossy J., Eur. J. Org. Chem., 2016, 2016, 5485–5493. https://doi.org/10.1002/ejoc.201600947
14. 14. Voronin V.V., Ledovskaya M.S., Gordeev E.G., Rodygin K.S., Ananikov V.P., J. Org. Chem., 2018, 83, 3819–3828. https://doi.org/10.1021/acs.joc.8b00155
15. 15. Vetrov D.E., Sazonov P.K., Beletskaya I.P., Titanyuk I.D., Russ. Chem. Bull., 2024, 73, 1011–1017. https://doi.org/10.1007/s11172-024-4215-9
16. 16. Zeng J.-L., Chen Z., Zhang F.-G., Ma J.-A., Org. Lett., 2018, 20, 4562–4565. https://doi.org/10.1021/acs.orglett.8b01854
17. 17. Candish L., Collins K.D., Cook G.C., Douglas J.J., Gómez-Suárez A., Jolit A., Keess S., Chem. Rev., 2022, 122, 2907–2980. https://doi.org/10.1021/acs.chemrev.1c00416
18. 18. Barata-Vallejo S., Cooke M.V., Postigo A., ACS Catal., 2018, 8, 7287–7307. https://doi.org/10.1021/acscatal.8b02066
19. 19. Barata-Vallejo S., Bonesi S.M., Postigo A., Org. Biomol. Chem., 2015, 13, 11153–11183. https://doi.org/10.1039/c5ob01486g
20. 20. Koike T., Akita M., Top. Catal., 2014, 57, 967–974. https://doi.org/10.1007/s11244-014-0259-7
21. 21. Levin V.V., Dilman A.D., Chem. Rec., 2023, 23, e202300038. https://doi.org/10.1002/tcr.202300038
22. 22. Sladojevich F., McNeill E., Börgel J., Zheng S.-L., Ritter T., Angew. Chem. Int. Ed., 2015, 54, 3712–3716. https://doi.org/10.1002/anie.201410954
23. 23. Qian H.-Y., Wang Z.-L., Chen L.-L., Pan Y.-L., Xie X.-Y., Xie X., Chen J.-Z., ChemMedChem, 2018, 13, 2455–2463. https://doi.org/10.1002/cmdc.201800541
24. 24. Waring M.J., Clarke D.S., Fenwick M.D., Godfrey L., Groombridge S.D., Johnstone C., McKerrecher D., Pike K.G., Rayner J.W., Robb G.R., Wilson I., MedChemComm, 2012, 3, 1077–1081. https://doi.org/10.1039/C2MD20077E
25. 25. Berthel S.J., Kester R.F., Murphy D.E., Prins T.J., Ruebsam F., Sarabu R., Tran C.V., Vourloumis D., US20080021032, 2008.
26. 26. Koltun D.S., Dilman A.D., Mendeleev Commun., 2024, 34, 531–532. https://doi.org/10.1016/j.mencom.2024.06.020
27. 27. McGee K.A., Veltkamp D.J., Marquardt B.J., Mann K.R., J. Am. Chem. Soc., 2007, 129, 15092–15093. https://doi.org/10.1021/ja0681772