Relevant bibliographies by topics / Potassium phthalimide

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Academic literature on the topic 'Potassium phthalimide'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Potassium phthalimide"

1

Nagel, N., H. Bock, and J. W. Bats. "Potassium Phthalimide." Acta Crystallographica Section C Crystal Structure Communications 52, no. 6 (1996): 1344–46. http://dx.doi.org/10.1107/s0108270196002387.

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2

Basu, Souradeep, Alexander H. Sandtorv, and David R. Stuart. "Imide arylation with aryl(TMP)iodonium tosylates." Beilstein Journal of Organic Chemistry 14 (May 11, 2018): 1034–38. http://dx.doi.org/10.3762/bjoc.14.90.

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Herein, we describe the synthesis of N-aryl phthalimides by metal-free coupling of potassium phthalimide with unsymmetrical aryl(TMP)iodonium tosylate salts. The aryl transfer from the iodonium moiety occurs under electronic control with the electron-rich trimethoxyphenyl group acting as a competent dummy ligand. The yields of N-aryl phthalimides are moderate to high and the coupling reaction is compatible with electron-deficient and sterically encumbered aryl groups.
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3

Ogurtsov, Vladimir A., and Oleg A. Rakitin. "8,18-Dithia-1,4,11,14-tetraazapentacyclo[11.7.0.03,11.05,9.015,19]icosa-3,5(9),6,13,15(19),16-hexaene-10,20-dione." Molbank 2019, no. 2 (2019): M1056. http://dx.doi.org/10.3390/m1056.

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4H-3λ2-Thieno[3,2-d]pyrimidin-4-one derivatives are of interest as biologically active compounds. In this communication, 2-(chloromethyl)-4H-3λ2-thieno[3,2-d]pyrimidin-4-one (1) was investigated in the reaction with ammonia, potassium phthalimide, and other basic agents. The dimerization product—8,18-dithia-1,4,11,14-tetrazapentacyclo[11.7.0.03,11.05,9.015,19]icosa-3,5(9),6,13,15(19),16-hexaene-10,20-dione was formed in the reaction with potassium phthalimide in DMF, by heating at 110 °C for 5 h. The structure of the newly synthesized compound was established by means of elemental analysis, hi
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4

Mercer, Frank W. "Synthesis and characterization of aromatic poly(ether ketone amide)s." High Performance Polymers 5, no. 3 (1993): 187–96. http://dx.doi.org/10.1088/0954-0083/5/3/002.

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A general method for the preparation of amide-containing aromatic polyether ketones has been developed. Polymerization is based on a ketone-activated halo displacement in amide-containing bis(4-fluorobenzoyl) moieties by phenoxides. N,N-Bis[4-(4-fluorobenzoyl)-(4-phenoxyphenylJ]terephthalamide and 4-[(4-fiuorobenzoyl)-(4-phenoxyphenylcarbamoyl)]-N-[(4-fluorobenzoyl)-(4-phenoxyphenyl)]phthalimide were prepared by reaction of 4-fluoro-benzoyl chloride with N,N.bis(4-phenoxyphenyl)terephthalamide and 4-(4.phenoxy-phenylcarbamoyl)-N-(4-phenoxyphenyl)phthalimide, respectively, in dichloromethane in
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5

Takahashi, Hiroki. "N-(4-Methoxybenzyl)phthalimide: a triclinic polymorph." Acta Crystallographica Section E Structure Reports Online 68, no. 8 (2012): o2457—o2458. http://dx.doi.org/10.1107/s1600536812031376.

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The title compound [systematic name: 2-(4-methoxybenzyl)isoindoline-1,3-dione], C16H13NO3, represents a triclinic polymorph of the previously reported monoclinic form [Warzechaet al.(2006).Acta Cryst. E62, o5450–o5452]. The reaction of potassium phthalimide and 4-methoxybenzyl chloride in dimethylformamide gave platelet-shaped crystals; these were harvested and then needle-shaped crystals were deposited. The platelet- and needle-shaped crystals correspond to the triclinic and monoclinic forms, respectively. The N—C—Car—Cartorsion angles between the ring systems are −82.66 (14) and 95.28 (13)°,
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6

Tibebu, Berihun, Abdudin Geremu, and Endale Tsegaye. "DFT Study on Potassium Benzene Disulfonamide and Potassium Phthalimide Ionic Liquid Based Carbon Dioxide Absorption." International Journal of Computational and Theoretical Chemistry 13, no. 1 (2025): 25–42. https://doi.org/10.11648/j.ijctc.20251301.13.

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This groundbreaking research rigorously investigated the CO<sub>2</sub> absorption potential of two potassium-based ionic liquids (ILs), namely potassium benzene disulfonamide [C<sub>6</sub>H<sub>4</sub>KNS<sub>2</sub>O<sub>4</sub>] and potassium phthalimide [C<sub>8</sub>H<sub>4</sub>KNO<sub>2</sub>]. Driven by the urgent need for effective carbon capture technologies to c
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7

Hekmatshoar, R., M. M. Heravi, B. Baghernejad, and K. Asadolah. "MICROWAVE-ASSISTED N-ALKYLATION OF POTASSIUM PHTHALIMIDE AND POTASSIUM SUCCINIMIDE ONTO SILICA GEL IN DRY MEDIA." Phosphorus, Sulfur, and Silicon and the Related Elements 179, no. 8 (2004): 1611–14. http://dx.doi.org/10.1080/10426500490466157.

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8

Kiyani, Hamzeh, and Maryam Bamdad. "One-Pot and Efficient Synthesis of 5-Aminopyrazole-4-carbonitriles Catalyzed by Potassium Phthalimide." HETEROCYCLES 94, no. 2 (2017): 276. http://dx.doi.org/10.3987/com-16-13623.

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9

Dekamin, Mohammad G., and Zahra Karimi. "Activation of trimethylsilyl cyanide by potassium phthalimide for facile synthesis of TMS-protected cyanohydrins." Journal of Organometallic Chemistry 694, no. 12 (2009): 1789–94. http://dx.doi.org/10.1016/j.jorganchem.2009.01.058.

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10

Zhang, Shuai, Yu-Nong Li, Ya-Wei Zhang, et al. "Equimolar Carbon Absorption by Potassium Phthalimide and In Situ Catalytic Conversion Under Mild Conditions." ChemSusChem 7, no. 5 (2014): 1484–89. http://dx.doi.org/10.1002/cssc.201400133.

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Book chapters on the topic "Potassium phthalimide"

1

Sakya, S. M., and J. Yang. "Substituted 1,4-Dioxins by Reaction of Methyl 3-Chloro-2-oxo-3-phenylpropanoate with Potassium Phthalimide or Sodium Imidazolide." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-116-00511.

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