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Relevant bibliographies by topics / 3-pyrrolin-2-one derivatives

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Academic literature on the topic '3-pyrrolin-2-one derivatives'

Author: Grafiati

Published: 24 April 2022

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Journal articles on the topic "3-pyrrolin-2-one derivatives"

1

Kocharyan, S. T., N. P. Churkina, T. L. Razina, et al. "New method for synthesis of 3-pyrrolin-2-one derivatives." Chemistry of Heterocyclic Compounds 30, no. 10 (1994): 1165–69. http://dx.doi.org/10.1007/bf01184878.

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2

Moshtaghi Zonouz, Adeleh, Issa Eskandari, and Behrooz Notash. "Efficient Synthesis of 3-Pyrrolin-2-one Derivatives in Aqueous Media." Synthetic Communications 45, no. 18 (2015): 2115–21. http://dx.doi.org/10.1080/00397911.2015.1065506.

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3

Gerasimova, Daria, Robert R. Fayzullin, Alina Saifina, Irina Vandyukova, Almira Kurbangalieva, and Olga Lodochnikova. "Unexpected polymorphic behaviour of four racemic 3-pyrrolin-2-one derivatives." Acta Crystallographica Section A Foundations and Advances 75, a2 (2019): e463-e463. http://dx.doi.org/10.1107/s2053273319090934.

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4

Tedjar, Farouk, Salah Ymmel, Miroslav Janda, Petr Duchek, Petr Holý, and Ivan Stibor. "Electrochemical oxidation of pyrrole derivatives in alcoholic medium." Collection of Czechoslovak Chemical Communications 54, no. 5 (1989): 1299–305. http://dx.doi.org/10.1135/cccc19891299.

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Abstract:

Electrochemical oxidation of pyrrole (I), 1-methylpyrrole (II), 1,2,5-trimethylpyrrole (III), methyl 1-methyl-2-pyrrolecarboxylate (IV) and diethyl 3,5-dimethyl-2,4-pyrroledicarboxylate (V) has been studied. An advantageous method of preparation of polypyrroles (PP) and conductive PVC-PP composites has been elaborated, permitting a 20 fold starting concentration of the monomer. Electrooxidation of II in methanol leads either to 5,5-dimethoxy-1-methyl-3-pyrrolin-2-one (VII) or 1-methyl-2,2,5,5-tetramethoxy-3-pyrroline (VI), their ratio depending on water content in the alcohol used. Oxidation of IV affords the analogous 5-carbomethoxy-5-methoxy-1-methyl-3-pyrrolin-2-one (X), oxidation of III and V leads to products of substitution at the methyl groups.

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5

KURITA, JYOJI, KAZUKO TAKAYAMA, and TAKASHI TSUCHIYA. "Photolysis of pyridazin-3-one 1-imides: Ring contraction into 3-pyrrolin-2-one derivatives." CHEMICAL & PHARMACEUTICAL BULLETIN 33, no. 8 (1985): 3540–44. http://dx.doi.org/10.1248/cpb.33.3540.

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6

Rubtsova, Daria D., Alexandra A. Bobyleva, Daria D. Lezhnina, Sofia V. Polikarpova, Polina A. Rozhkova, and Vladimir L. Gein. "Synthesis of 5-aryl-3-hydroxy-1-(2-hydroxypropyl)-4-(furyl-2-carbonyl)- 3-pyrrolin-2-ones and 5-aryl-3-hydroxy-1-(3-hydroxypropyl)- 4-(furyl-2-carbonyl)-3-pyrrolin-2-ones." Butlerov Communications 63, no. 9 (2020): 26–30. http://dx.doi.org/10.37952/roi-jbc-01/20-63-9-26.

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Abstract:

In this work, pyrrolidin-2-ones and their derivatives are considered as a promising class of non-aromatic heterocyclic compounds. Their structure is found in the nuclei of many natural products and biologically active molecules. In pharmacy the possibility of introducing various substituents into the nucleus of pyrrolidin-2-ones is a great importance for the synthesis of new medicinal molecules with improved biological activity. Nowadays the synthesis of new active compounds by introducing various substituents at the C1-, C4- and C5-position of 3-hydroxy-3-pyrrolin-2-one has been little studied and it is of great interest to study the conditions of their synthesis, chemical properties and biological activity. In this research work the corresponding 5-aryl-3-hydroxy-1-(2-hydroxypropyl)-4-(furyl-2-carbonyl)-3-pyrrolin-2-ones and 5-aryl-3-hydroxy-1-(3-hydroxypropyl)-4-(furyl-2-carbonyl)-3-pyrrolin-2-ones were synthesized by the reaction of methyl ester of furyl-2-carbonylpyruvic acid with a mixture of aromatic aldehyde and 1-amino-2-hydroxypropane or 3-amino 1-hydroxypropane when heated in dioxane. The results of the study of the structure of the new synthesized compounds are presented. The structure was proved using 1H NMR spectroscopy and IR spectrometry. It was shown that the IR spectra of the compounds contain bands of the corresponding stretching vibrations of the alcoholic hydroxyl group, enol hydroxyl, amide and ketone groups. In the 1H NMR spectra of the compounds, along with the signals of aromatic protons in the C5 substituent and related groups, characteristic peaks are observed, indicating the formation of the corresponding derivatives of 3-hydroxy-3-pyrrolin-2-ones. It was noted that in the case of the synthesis of 5-aryl-3-hydroxy-1-(2-hydroxypropyl)-4-(furyl-2-carbonyl)-3-pyrrolin-2-ones, the signal of the methine proton at the C5 position of the heterocycle is cleaved in 1H NMR spectra compounds as a result of the appearance of a second chiral center in the 2-hydroxypropyl radical. Elemental analysis was performed for the synthesized compounds.

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7

IKEGUCHI, Masahiko, Masahiko SAWAKI, Hiroshi YOSHII, Kazuyuki MAEDA, and Yasuo MORISHIMA. "Synthesis and Herbicidal Activity of 1-Arylalkyl-3-pyrrolin-2-one Derivatives." Journal of Pesticide Science 25, no. 2 (2000): 107–16. http://dx.doi.org/10.1584/jpestics.25.107.

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8

Moshtaghi Zonouz, Adeleh, Issa Eskandari, and Behrooz Notash. "ChemInform Abstract: Efficient Synthesis of 3-Pyrrolin-2-one Derivatives in Aqueous Media." ChemInform 46, no. 52 (2015): no. http://dx.doi.org/10.1002/chin.201552102.

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9

KOCHARYAN, S. T., N. P. CHURKINA, T. L. RAZINA, et al. "ChemInform Abstract: A New Method for the Synthesis of 3-Pyrrolin-2-one Derivatives." ChemInform 26, no. 28 (2010): no. http://dx.doi.org/10.1002/chin.199528111.

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10

Ribó, Josep M., and Asunción Vallés. "MNDO and MINDO/3 study of the reactivity of 3-pyrrolin-2-one tautomers and derivatives." Journal of Heterocyclic Chemistry 24, no. 2 (1987): 457–64. http://dx.doi.org/10.1002/jhet.5570240229.

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