N. V. Palysaeva, N. S. Boltacheva, P. A. Slepukhin, M. G. Pervova, V. I. Filyakova, A. B. Sheremetev, V. N. Charushin, “Step by step and one-pot syntheses of 5-hydroxy-5-(polyfluoroalkyl)isoxazol-4(5H)-one oximes”, Mendeleev Commun., 28:2 (2018), 126–127

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Mendeleev Communications, 2018, Volume 28, Issue 2, Pages 126–127
DOI: https://doi.org/10.1016/j.mencom.2018.03.003 (Mi mendc1685)

This article is cited in 8 scientific papers (total in 8 papers)

Communications

Step by step and one-pot syntheses of 5-hydroxy-5-(polyfluoroalkyl)isoxazol-4(5H)-one oximes

N. V. Palysaeva^a, N. S. Boltacheva^b, P. A. Slepukhin^b, M. G. Pervova^b, V. I. Filyakova^b, A. B. Sheremetev^a, V. N. Charushin^bc

^a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^b I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
^c Department of Chemistry, Ural Federal University, Ekaterinburg, Russian Federation

Full-text PDF (293 kB) Citations (8)

DOI: https://doi.org/10.1016/j.mencom.2018.03.003

Graphic abstract: Step by step and one-pot syntheses of 5-hydroxy-5-(polyfluoroalkyl)isoxazol-4(5<i>H</i>)-one oximes

Abstract: 5-Hydroxy-5-(polyfluoroalkyl)isoxazol-4(5H)-one oximes have been obtained by nitrosation of lithium 3-polyfluoroalkyl-1,3-diketonates followed by treatment of intermediate 3-(poly-fluoroalkyl)propane-1,2,3-trione 2-oximes with hydroxylamine hydrochloride. The one-pot protocol comprising both stages has been elaborated.

Document Type: Article

Language: English

*Supplementary materials:*
		Supplementary_data_1.pdf	(436.0 Kb)

Citation: N. V. Palysaeva, N. S. Boltacheva, P. A. Slepukhin, M. G. Pervova, V. I. Filyakova, A. B. Sheremetev, V. N. Charushin, “Step by step and one-pot syntheses of 5-hydroxy-5-(polyfluoroalkyl)isoxazol-4(5H)-one oximes”, Mendeleev Commun., 28:2 (2018), 126–127

Linking options:

https://www.mathnet.ru/eng/mendc1685

https://www.mathnet.ru/eng/mendc/v28/i2/p126

This publication is cited in the following 8 articles:

Garima Sumran, Naman Jain, Prince Kumar, Ranjana Aggarwal, “Trifluoromethyl‐β‐dicarbonyls as Versatile Synthons in Synthesis of Heterocycles”, Chemistry A European J, 30:11 (2024)
N. S. Boltacheva, T. I. Filyakova, M. I. Kodess, M. A. Ezhikova, P. A. Slepukhin, V. I. Filyakova, V. I. Saloutin, V. N. Charushin, “3-(Trifluoromethyl)-1,2,3-propanetrione 2-oximes in the synthesis of new heterocyclic systems”, Russ Chem Bull, 72:3 (2023), 706
Vera I. Filyakova, Nadezhda S. Boltacheva, Pavel A. Slepukhin, Valery N. Charushin, “Efficient one-pot synthesis of 3-(polyfluoroalkyl)pyrazol-4-amines”, Chem Heterocycl Comp, 59:8 (2023), 546
N. A. Pulina, F. V. Sobin, T. A. Yushkova, V. V. Novikova, “Reactions of 4-aryl-N-hetaryl-2-hydroxy-4-oxobut-2-enamides with hydroxylamine and biological activity of the products”, Russ Chem Bull, 68:3 (2019), 628
N. S. Boltacheva, P. A. Slepukhin, M. G. Pervova, V. I. Filyakova, V. N. Charushin, “Reactions of 3-(Polyfluoroalkyl)propane-1,2,3-trione-2-oximes with Diaminoarenes”, Russ J Gen Chem, 89:3 (2019), 416
P. A. Slepukhin, N. S. Boltacheva, V. I. Filyakova, V. N. Charushin, “Synthesis and structure of lithium 3-trifluoromethyl-1,3-diketonates containing pyridyl substituents”, Russ Chem Bull, 68:6 (2019), 1213
V. I. Filyakova, N. S. Boltacheva, V. N. Charushin, “Synthesis of 3-Aroyl-2-(polyfluoroalkyl)quinoxalines and 3-Aroyl-2-(polyfluoroalkyl)benzo[g]quinoxalines from Lithium 3-(Fluoroalkyl)-1,3-diketonates”, Russ J Org Chem, 55:6 (2019), 890
D. V. Belyaev, D. L. Chizhov, M. I. Kodess, M. A. Ezhikova, G. L. Rusinov, V. N. Charushin, “Synthesis of 2-(polyfluoromethyl)pyrimido-[1,2-a]benzimidazole-4-carbaldehyde derivatives”, Mendeleev Commun., 29:3 (2019), 249–251

Citing articles in Google Scholar: Russian citations, English citations
Related articles in Google Scholar: Russian articles, English articles

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