Method of synthesis of 4-substituted 3-nitrophenyl carbonyls from benzyl alcohols
- Autores: Kazantsev D.A.1, Denisov A.A.1,2, Pestov A.V.1,2
-
Afiliações:
- I.Ya. Postovsky Insititute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences
- Ural Federal University
- Edição: Volume 60, Nº 12 (2024)
- Páginas: 1209-1215
- Seção: Articles
- URL: https://aspvestnik.ru/0514-7492/article/view/681813
- DOI: https://doi.org/10.31857/S0514749224120047
- EDN: https://elibrary.ru/AQMXWT
- ID: 681813
Citar
Resumo
A method has been developed for the production of 4-substituted-3-nitrophenyl carbonyl s based on the tandem oxidation and nitration process of benzyl alcohols. The proposed method is single-reactor and makes it possible to obtain target compounds with good yield, under mild conditions, using stable commercially available starting substances.
Texto integral

Sobre autores
Daniil Kazantsev
I.Ya. Postovsky Insititute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences
Autor responsável pela correspondência
Email: daniil_kazantsev@mail.ru
ORCID ID: 0009-0008-8648-3395
Rússia, Sofya Kovalevskaya st., 22/20, Yekaterinburg, 620108
Alexander Denisov
I.Ya. Postovsky Insititute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences; Ural Federal University
Email: daniil_kazantsev@mail.ru
ORCID ID: 0009-0000-4715-8284
Ural Federal University, The Institute of Natural Sciences and Mathematics
Rússia, Sofya Kovalevskaya st., 22/20, Yekaterinburg, 620108; Kuibysheva st., 48, Yekaterinburg, 620026Alexander Pestov
I.Ya. Postovsky Insititute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences; Ural Federal University
Email: daniil_kazantsev@mail.ru
ORCID ID: 0000-0002-4270-3041
Ural Federal University, The Institute of Natural Sciences and Mathematics
Rússia, Sofya Kovalevskaya st., 22/20, Yekaterinburg, 620108; Kuibysheva st., 48, Yekaterinburg, 620026Bibliografia
- Pease A.C., Solas D., Sullivan E.J., Cronin M.T., Holmes C.P., Fodor S.P. Biochemistry. 1994, 91 (11), 5022–5026. doi: 10.1073/pnas.91.11.5022
- Kretcchy N., Holik A.-K., Somoza V., Stengele K.-P., Somoza M. M. Angew. Chem. Int. Ed. 2015, 54 (29), 8555–8559.
- Stengele K.-P. Международная заявка. WO 2012/136604. C.A. 2012, 136604 A1.
- Klan P., Solomek T., Bochet C.G., Blank A., Givens R., Rubina M., Popik V., Kostikov A., Wirz J. Chem. Rev. 2013, 113, 119–191. doi: 10.1021/cr300177k
- Grigor'ev E.I., Zhil'tsov O.S. Russ. J. Org. Chem., 1989, 25 (9), 1963–1967.
- Chandrappa S., Sadashiva M. P., Rangappa K.S. Synth. Commun. 2008, 38 (15), 2638–2645. doi: 10.1080/00397910802219502
- Somey M. Chem. Pharm. Bull., 1986, 34 (10), 4109–4115. doi: 10.1248/cpb.34.4109
- Saaidin A.S., Murai Y., Ishikawa T., Monde K. Eur. J. Org. Chem. 2019, 46, 7563–7567. doi: 10.1002/eJoc.201901348
- Flitsch W., Russkamp P., Langer W. Liebigs Ann. Chem., 1985, 7, 1413–1421. doi: 10.1002/chin.198546320
- Swoboda P., Saf R., Hummel K., Hofer F., Czaputa R. Macromolecules. 1995, 28 (12), 4255–4259. doi: 10.1021/ma00116a028
- Bykov V.V., Korolev D.N., Bumagin N.A. Russ. Chem. Bull. 1997, 46, 1631–1632. doi: 10.1007/BF02502959
- Strazzolini P., Runcio A. Eur. J. Org. Chem. 2003, 3, 526–536. doi: 10.1002/eJoc.200390090
Arquivos suplementares
