Relevant bibliographies by topics / Synthesis of 3-pyrrolin-2-one

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Academic literature on the topic 'Synthesis of 3-pyrrolin-2-one'

Author: Grafiati
Published: 24 April 2022

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Journal articles on the topic "Synthesis of 3-pyrrolin-2-one"

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

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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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 studie
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3

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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4

Gein, Vladimir L., and Evgenia V. Pastukhova. "Synthesis and properties of 1-aminocarbonylmethyl-5-aryl- 4-aroyl-3-hydroxy-3-pyrroline-2-ones." Butlerov Communications 64, no. 10 (2020): 28–32. http://dx.doi.org/10.37952/roi-jbc-01/20-64-10-28.

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3-Hydroxy-3-pyrrolin-2-ones are fully hydrogenated heterocyclic compounds, the base of which is included in a number of biologically active substances and drugs. Scientists' interest in 3-Hydroxy-3-pyrrolin-2-ones is due to the fact that, with their availability and high stability, they also have high reactivity due to the active carbonyl group in the third position of the heterocycle and easily interact with moconucleophiles. In addition, the presence of acyl and ethoxycarbonyl groups in the fourth position of the heterocycle makes it possible to obtain various condensed systems in reactions
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5

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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6

Ahankar, Hamideh, Ali Ramazani, Katarzyna Ślepokura, Tadeusz Lis, and Sang Woo Joo. "Synthesis of pyrrolidinone derivatives from aniline, an aldehyde and diethyl acetylenedicarboxylate in an ethanolic citric acid solution under ultrasound irradiation." Green Chemistry 18, no. 12 (2016): 3582–93. http://dx.doi.org/10.1039/c6gc00157b.

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7

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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8

Hsu, Ming-Tsung, Yi-Hung Liu, and Shiuh-Tzung Liu. "Synthesis of 2-Benzylidene-3-Pyrrolines and Their Synthetic Transformation." Reactions 1, no. 2 (2020): 47–53. http://dx.doi.org/10.3390/reactions1020005.

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A series of benzylidene-3-pyrrolines were prepared from chalcone derivatives, arylacetylene and sulfonamide via a three-step sequence without the isolation of intermediates. Typically, the reaction of 1,3-di-p-tolylprop-2-en-1-one with lithium phenylacetylide was followed by substitution with tosylamide and then silver-catalyzed 5-exo-dig cyclization to give N-tosyl-2-benzylidene-3,5-di-p-tolyl-2,5-dihydro-1H-pyrrole with a 86% yield. Furthermore, transformation to the corresponding substituted 3-pyrrolin-2-one and pyrrole by m-chloroperbenzoic acid (mcpba)-oxidation and acid-catalyzed aromati
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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

Ryabova, S. Yu, Yu I. Trofimkin, L. M. Alekseeva, I. F. Kerbnikova, G. Ya Shvarts, and V. G. Granik. "Synthesis and biological activity of dienediaminoketones of the indolin-3-one and 2-pyrrolin-4-one series." Pharmaceutical Chemistry Journal 29, no. 9 (1995): 610–17. http://dx.doi.org/10.1007/bf02226389.

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