Relevant bibliographies by topics / Phenyl succinimide

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Academic literature on the topic 'Phenyl succinimide'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Phenyl succinimide"

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Ravindra, Dhivare, Chaudhari Prashant, and Rajput Shankarsing. "Synthesis of Pyridine and Phenyl Succinimides by Green Pathway and Their Antimicrobial Assay." American Journal of Heterocyclic Chemistry 4, no. 1 (2018): 26–29. https://doi.org/10.11648/j.ajhc.20180401.13.

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<strong>Abstract </strong> A simple and clean green method was implemented for the preparation of different <strong><em>succinimide derivatives</em></strong> by means of the N-substituted anilines or N-substituted 2-aminopyridines with succinic anhydride with the heating in an aqueous medium. The total synthesized 3a-j compounds were evaluated against antibacterial and antifungal species.
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Boudriga, Sarra, Saoussen Haddad, Vikneswaran Murugaiyah, et al. "Three-Component Access to Functionalized Spiropyrrolidine Heterocyclic Scaffolds and Their Cholinesterase Inhibitory Activity." Molecules 25, no. 8 (2020): 1963. http://dx.doi.org/10.3390/molecules25081963.

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A novel one-pot [3+2]-cycloaddition reaction of (E)-3-arylidene-1-phenyl-succinimides, cyclic 1,2-diketones (isatin, 5-chloro-isatin and acenaphtenequinone), and diverse α-aminoacids such as 2-phenylglycine or sarcosine is reported. The reaction provides succinimide-substituted dispiropyrrolidine derivatives with high regio- and diastereoselectivities under mild reaction conditions. The stereochemistry of these N-heterocycles has been confirmed by four X-ray diffraction studies. Several synthetized compounds show higher inhibition on acetylcholinesterase (AChE) than butyrylcholinesterase (BChE
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Dobre, Adela F., Augustin M. Madalan, and Petre Ionita. "The Crystal Structures of Some Bromo-Derivatives of the DPPH Stable Free Radical." Molbank 2024, no. 3 (2024): M1880. http://dx.doi.org/10.3390/m1880.

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Bromination of the 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical with bromine or N-bromo-succinimide (NBS) affords a complex mixture of bromo- and nitro-derivatives of the starting material. In this study, by chromatographic separation, most of the reaction products were isolated. Suitable crystals for X-ray measurements were obtained and characterized for the compounds 2-p-bromophenyl-2-phenyl-1-picrylhydrazyl free radical (Br-DPPH), 2-p-bromophenyl-2-phenyl-1-picrylhydrazine (Br-DPPH-H), and 2,2-(p-bromophenyl)-1-(2-bromo-4,6-dinitrophenyl)hydrazine (Br2-DPPBr-H).
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Ravindra, S. Dhivare, and S. Rajput Shankarsing. "Synthesis, physicochemical probe and antimicrobial assay of bis-chalcone, pyrazole, amino-pyrimidine and malononitrile derivatives from five and six membered cyclic imides." Iranian Journal of Organic Chemistry 8, no. 4 (2017): 1909–18. https://doi.org/10.5281/zenodo.3911281.

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<strong>Abstract </strong> Heterocyclic imides greatly involved in the development of organic synthesis. Coloured flavonoids like bis-chalcones are formed by microwave-assisted solvent-free route using phenyl succinimide, glutarimide, and vanillin. To achieve the <em><strong>pyrazole</strong></em> and <strong><em>amino-pyrimidine</em></strong> derivatives by the cyclization of bis-chalcone with hydrazine hydrate and guanidine nitrate via microwave method. Then <strong><em>dimalononitriles</em></strong> were produced by the active methylene group of dinitrile with cyclic imides. Hence the physi
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5

Li, Shao-Hua, and et al. "Crystal structure of 3,4-bis-(acetyloxy)-N-phenyl-succinimide, C14H13NO6." Zeitschrift für Kristallographie - New Crystal Structures 227, no. 3 (2012): 375–76. http://dx.doi.org/10.1524/ncrs.2012.0190.

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6

R.S., Dhivare, S. Rajput S., and Yadav R. "Synthesis of new series of N-substituted phenyl succinimide and glutarimide derivatives for the study of their antifungal activity." International Journal of Chemical Studies 4, no. 1 (2015): 61–63. https://doi.org/10.5281/zenodo.3911256.

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<strong>Abstract</strong> A new series of <strong><em>N-substituted phenyl cyclic imides</em></strong> were synthesized via the reaction between succinic, glutaric anhydride, and primary aromatic amines in presence of benzene and acetyl chloride. The synthesized derivatives were characterized by IR, <sup>1</sup>HNMR, and <sup>13</sup>CNMR spectroscopy, and antifungal activity behavior was studied using the disc diffusion method.
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V., Mishra. "Coordination polymers of copper( II) imides with polymeric heterocyclic Schiff bases of thiazole derivatives." Journal of India Chemical Society Vol. 79, Apr 2002 (2002): 374–75. https://doi.org/10.5281/zenodo.5849358.

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Department of Post- Graduate Studies in Chemistry, Nehru College, Chhibramau-209 721, India <em>Manuscript received 29 September 2000. revised 26 July 2001. accepted 1 September 2001</em> Two polymeric ligands, L<sub>1</sub> and L<sub>2</sub> were synthesized by polymerizing new heterocyclic Schiff bases 2-hydroxy-1-benzylidene-2-amino&middot; 4-phenylthiazole and 2-hydroxy-1-benzylidene-2-amino-4-phenyl-5-phenylazothiazole, with 1,6-dichlorohexane. L<sub>1</sub>. L<sub>2</sub> gave solid chelates with copper( II) phthalimide or succinimide. The metal ion is coordinated through nitrogen of imi
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8

Mutlaq, Dakhil Z., Ali A. A. Al-Shawi, and Rafid H. Al-Asadi. "Synthesis, characterization, anticancer activity, and molecular docking of novel maleimide–succinimide derivatives." Egyptian Pharmaceutical Journal 20, no. 4 (2021): 303–12. http://dx.doi.org/10.4103/epj.epj_26_21.

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Background and objective A wide range of maleimide heterobifunctional reagents are used for the preparation of targeted therapeutics. Succinimide derivatives are important compounds found in a variety of natural products that exhibit remarkable biological and pharmaceutical activity. The creation of new maleimide–succinimide derivatives will increase the importance and medicinal applications of these groups. Materials and methods The reaction of bismaleimide (1–2) with phenylhydrazide and 4-methylbenzohydrazide resulted in the formation of N’-[1-(4-[2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl] phenyl
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9

Mahi, Ahmed, M. Belbachir, Abdelkader Ammari, R. Meghaber, and M. I. Ferrahi. "Synthesis and characterization of poly(N-phenyl succinimide-thiophene) conducting polymer catalyzed by Maghnite-H+." Journal of Electroanalytical Chemistry 823 (August 2018): 92–97. http://dx.doi.org/10.1016/j.jelechem.2018.05.039.

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10

Hambley, TW, IA Newsom, and S. Sternhell. "The Structure of (1'RS, 2SR,3RS,4'SR)-2,3-(Cyclohex-2′-en-1′, 4′-ylene)-N-(4″-methyl-phenyl)succinimide." Australian Journal of Chemistry 38, no. 3 (1985): 513. http://dx.doi.org/10.1071/ch9850513.

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A single-crystal X-ray structure determination gave the crystal and molecular parameters of\ (1′RS,2SR,3RS,4′SR)-2,3-(cyclohex-2′-en-1′,4′- ylene )-N-(4′-methylphenyl) succinimide , including the positions of all hydrogen atoms and the conformation of the 4′-methylphenyi group. The latter is possibly controlled by steric interactions between the ortho hydrogen atoms on the 4″-methylphenyl ring and the carbonyl oxygen atoms of the imide moiety. The six atoms of the imide moiety [O(10), C(9), N(8), C(13), O(14) and C(5) on the ORTEP plot in Fig. 1] are planar within 0.04 Ǻ.
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Conference papers on the topic "Phenyl succinimide"

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Chang, Ta-Chau, Chien-Chih Chiang, and Konan Peck. "Conformational Structures of Dye-Oligonucleotides Studied by Satellite Holes." In Biomedical Optical Spectroscopy and Diagnostics. Optica Publishing Group, 2006. http://dx.doi.org/10.1364/bosd.1996.dr5.

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The spectral features of satellite holes in nonphotochemical hole burned spectra provide a promising method to identify different conformational structures of chromophore-oligonucleotides. Different hole burned spectra are observed when a 4,4-difluoro-5-(4-phenyl-l,3-butadienyl)-4-bora-3a,4a-diaza-s-indacene-3-propionic acid, succinimidyl ester (BODIPY) molecule is chemically bound to oligonucleotides of different base compositions, implying that different conformational structures exist among them. The study of satellite holes reveals that the conformational structure of BODIPY-oligonucleotid
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