Photocatalytic Fluoroalkylation of Derivatives of 3-Aminopyrazole
- Authors: Koltun D.S.1, Levin V.V.1, Dilman A.D.1
-
Affiliations:
- N.D. Zelinsky Institute of Organic Chemistry
- Issue: Vol 61, No 7 (2025)
- Pages: 893–898
- Section: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://journals.rcsi.science/0514-7492/article/view/376478
- DOI: https://doi.org/10.7868/S3034630425070109
- ID: 376478
Cite item
Abstract
About the authors
D. S. Koltun
N.D. Zelinsky Institute of Organic ChemistryMoscow, Russia
V. V. Levin
N.D. Zelinsky Institute of Organic ChemistryMoscow, Russia
A. D. Dilman
N.D. Zelinsky Institute of Organic Chemistry
Email: dilman@ioc.ac.ru
Moscow, Russia
References
- Inoue M., Sumii Y., Shibata N., ACS Omega, 2020, 5, 10633–10640. https://doi.org/10.1021/acsomega.0c00830
- Ogawa Y., Tokunaga E., Kobayashi O., Hirai K., Shibata N., iScience, 2020, 23, 101467. https://doi.org/10.1016/j.isci.2020.101467
- Nenajdenko V., Fluorine in Heterocyclic Chemistry. Springer International Publishing: Cham, Switzerland, 2014; Vol. 1 and 2.
- 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
- 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
- Pankov R.O., Prima D.O., Ananikov V.P., Coord. Chem. Rev., 2024, 516, 215897. https://doi.org/10.1016/j.ccr.2024.215897
- Schmidt A., Dreger A., Curr. Org. Chem., 2011, 15, 1423–1463. https://doi.org/10.2174/138527211795378263
- 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
- Mykhailiuk P.K., Chem. Rev., 2021, 121, 1670–1715. https://doi.org/10.1021/acs.chemrev.0c01015
- 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
- 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
- Dias H.V.R., Lovely C.J., Chem. Rev., 2008, 108, 3223–3238. https://doi.org/10.1021/cr078362d
- 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
- 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
- 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
- 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
- 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
- Barata-Vallejo S., Cooke M.V., Postigo A., ACS Catal., 2018, 8, 7287–7307. https://doi.org/10.1021/acscatal.8b02066
- Barata-Vallejo S., Bonesi S.M., Postigo A., Org. Biomol. Chem., 2015, 13, 11153–11183. https://doi.org/10.1039/c5ob01486g
- Koike T., Akita M., Top. Catal., 2014, 57, 967–974. https://doi.org/10.1007/s11244-014-0259-7
- Levin V.V., Dilman A.D., Chem. Rec., 2023, 23, e202300038. https://doi.org/10.1002/tcr.202300038
- 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
- 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
- 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
- Berthel S.J., Kester R.F., Murphy D.E., Prins T.J., Ruebsam F., Sarabu R., Tran C.V., Vourloumis D., US20080021032, 2008.
- Koltun D.S., Dilman A.D., Mendeleev Commun., 2024, 34, 531–532. https://doi.org/10.1016/j.mencom.2024.06.020
- 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
Supplementary files


