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Relevant bibliographies by topics / Tetrahydrophthalic acid

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Journal articles

Academic literature on the topic 'Tetrahydrophthalic acid'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Tetrahydrophthalic acid"

1

Klimova, E. I., V. N. Postnov, N. N. Meleshonkova, M. Martines Garcia, A. S. Zaks та V. V. Yushkov. "Biological activity of ferrocenyl-substituted derivatives of δ4-tetrahydrophthalic acid". Pharmaceutical Chemistry Journal 28, № 6 (1994): 401–5. http://dx.doi.org/10.1007/bf02285399.

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2

Iskenderova, S. A., N. F. Sadiyeva, L. M. Efendiyeva, Sh N. Asadova, Yu P. Cherepnova, and A. P. Musayeva. "New plasticizers for cellulose esters." Plasticheskie massy, no. 1-2 (March 19, 2020): 15–16. http://dx.doi.org/10.35164/0554-2901-2020-1-2-15-16.

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A method of obtaining of diesters and epoxy diesters of 3,6-endomethylene tetrahydrophthalic acid was studied. The conditions for the synthesis of diesters and epoxydiesters are found and their physic-chemical parameters are determined. A preliminary assessment of the possibility of using the synthesized epoxy diesters as plasticizers for cellulose esters was carried out. It was found that the new esters signiﬁcantly increase the physicomechanical properties of etrols.

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3

KLIMOVA, E. I., V. N. POSTNOV, N. N. MELESHONKOVA, M. MARTINEZ-GARCIA, A. S. ZAKS та V. V. YUSHKOV. "ChemInform Abstract: Biological Activity of Ferrocenyl-Substituted Derivatives of δ4- Tetrahydrophthalic Acid." ChemInform 25, № 48 (2010): no. http://dx.doi.org/10.1002/chin.199448202.

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4

Sun, Xuanrong, Yue Cai, Zhuomin Xu, and Dabu Zhu. "Preparation and Properties of Tumor-Targeting MRI Contrast Agent Based on Linear Polylysine Derivatives." Molecules 24, no. 8 (2019): 1477. http://dx.doi.org/10.3390/molecules24081477.

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We developed a tumor-targeted contrast agent based on linear polylysine (PLL) by conjugating a small molecular imaging agent, fluorescent molecule and targeting agent amino phenylboronic acid onto the amino groups of polylysine, which can specifically target monosaccharide sialic acid residues overexpressing on the surface of tumor cell membranes. Further, 3,4,5,6-Tetrahydrophthalic anhydride (DCA) was attached to the free amino groups of the polylysine to change to a negative charge at physiology pH to lower the cytotoxicity, but it soon regenerated to a positive charge again once reaching th

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5

Costa, Bianca B. C., Rogério Corrêa, Marcia M. De Souza, et al. "Antinociceptive Effects of Tetrahydrophthalimides and Related Compounds." Zeitschrift für Naturforschung C 62, no. 3-4 (2007): 201–6. http://dx.doi.org/10.1515/znc-2007-3-408.

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Abstract This paper describes the antinociceptive effects of tetrahydrophthalimides and related compounds in mice. Twenty compounds were obtained by the reaction of cis-1,2,3,6-tetrahydrophthalic anhydride with appropriate amines, dehydration, and addition to the imidic double bond. They were analyzed in the writhing test at 10 mg/kg given intraperitoneally. The most active compound 2-benzyl-5-morpholin-4-yl-hexahydroisoindole-1,3-dione (19) was studied on formalin, capsaicin, glutamate and hot plate models. The antinociceptive activity demonstrated by some studied compounds is promising, and

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6

Paprocka, Renata, Jolanta Kutkowska, Ewelina Paczkowska, Godwin Munroe Mwaura, Andrzej Eljaszewicz, and Anna Helmin-Basa. "Synthesis, Evaluation of Biological Activity, and Structure–Activity Relationships of New Amidrazone Derivatives Containing Cyclohex-1-ene-1-Carboxylic Acid." Molecules 30, no. 8 (2025): 1853. https://doi.org/10.3390/molecules30081853.

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In recent years, the incidence of acute and chronic inflammatory diseases has increased significantly worldwide, intensifying the search for new therapeutic agents, especially anti-inflammatory drugs. Therefore, the aim of this work was to synthesize, biologically assess, and explore the structure–activity relationships of new compounds containing the cyclohex-1-ene-1-carboxylic acid moiety. Six new derivatives, 2a–2f, were synthesized through the reaction of amidrazones 1a–1f with 3,4,5,6-tetrahydrophthalic anhydride. Their toxicity was evaluated in cultures of human peripheral blood mononucl

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7

Jönsson, B. A. G., C. H. Lindh, C. A. Gustavsson, H. Welinder, and P. Pfäffli. "Determination of cyclic organic acid anhydrides in air using gas chromatography. Part 2. Sampling and determination of hexahydrophthalic anhydride, methylhexahydrophthalic anhydride, tetrahydrophthalic anhydride and octenylsuccinic anhydride." Analyst 121, no. 9 (1996): 1285–90. http://dx.doi.org/10.1039/an9962101285.

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8

Baykov, Sergey V., Artem V. Semenov, Sofia I. Presnukhina та ін. "Hybrid 2D Supramolecular Organic Frameworks (SOFs) Assembled by the Cooperative Action of Hydrogen and Halogen Bonding and π⋯π Stacking Interactions". International Journal of Molecular Sciences 25, № 4 (2024): 2062. http://dx.doi.org/10.3390/ijms25042062.

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The cis- and trans-isomers of 6-(3-(3,4-dichlorophenyl)-1,2,4-oxadiazol-5-yl)cyclohex-3-ene-1-carboxylic acid (cis-A and trans-A) were obtained by the reaction of 3,4-dichloro-N′-hydroxybenzimidamide and cis-1,2,3,6-tetrahydrophthalic anhydride. Cocrystals of cis-A with appropriate solvents (cis-A‧½(1,2-DCE), cis-A‧½(1,2-DBE), and cis-A‧½C6H14) were grown from 1,2-dichloroethane (1,2-DCE), 1,2-dibromoethane (1,2-DBE), and a n-hexane/CHCl3 mixture and then characterized by X-ray crystallography. In their structures, cis-A is self-assembled to give a hybrid 2D supramolecular organic framework (S

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9

Suzuki, Kiyoshi, Takashi Kume, and Tetsuo Takematsu. "Herbicidal Selectivity of N-Acyl-N-phenyl-3,4,5,6-tetrahydrophthalamic Acid Derivatives under Paddy Conditions." Journal of Weed Science and Technology 42, no. 3 (1997): 206–13. http://dx.doi.org/10.3719/weed.42.206.

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10

Suzuki, Kiyoshi, Takashi Kume, and Tetsuo Takematsu. "Herbicidal Selectivity of Post-emergence N-Acyl-N-phenyl-3,4,5,6-tetrahydrophthalamic Acid Derivatives in Soybean." Journal of Weed Science and Technology 42, no. 3 (1997): 214–20. http://dx.doi.org/10.3719/weed.42.214.

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