Method of synthesis of 4-substituted 3-nitrophenyl carbonyls from benzyl alcohols
- Авторлар: Kazantsev D.A.1, Denisov A.A.1,2, Pestov A.V.1,2
-
Мекемелер:
- I.Ya. Postovsky Insititute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences
- Ural Federal University
- Шығарылым: Том 60, № 12 (2024)
- Беттер: 1209-1215
- Бөлім: Articles
- URL: https://permmedjournal.ru/0514-7492/article/view/681813
- DOI: https://doi.org/10.31857/S0514749224120047
- EDN: https://elibrary.ru/AQMXWT
- ID: 681813
Дәйексөз келтіру
Аннотация
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.
Толық мәтін

Авторлар туралы
Daniil Kazantsev
I.Ya. Postovsky Insititute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences
Хат алмасуға жауапты Автор.
Email: daniil_kazantsev@mail.ru
ORCID iD: 0009-0008-8648-3395
Ресей, 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
Ресей, 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
Ресей, Sofya Kovalevskaya st., 22/20, Yekaterinburg, 620108; Kuibysheva st., 48, Yekaterinburg, 620026Әдебиет тізімі
- 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
Қосымша файлдар
