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Journal articles on the topic 'Succinic Acid Derivatives'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Persson, T., A. B. Hörnfeldt, S. Gronowitz та N. G. Johansson. "Synthesis of Mimics to 5-(2″-thienyl)-2′,3′-β-Dideoxyuridine Triphosphate". Antiviral Chemistry and Chemotherapy 7, № 2 (1996): 101–7. http://dx.doi.org/10.1177/095632029600700207.

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A series of 5′-amido derivatives of 5-(2″-thienyl)-2′,3′,5′-β-trideoxyuridine were prepared. The compounds were tested for their inhibition of cellular DNA polymerase α and α HIV-RT. The succinic fumaric and maleic acid derivatives of 5-(2″-thienyl)-2′,3′,5′-β-trideoxyuridine were investigated. None of the compounds inhibited HIV-RT. The fumaric acid derivative inhibited DNA pol α with IC50 33 μg ml−1. The succinic acid derivative was about half as active with IC50 76 μg ml−1. The 5′-N-acyl derivatives also were structurally compared to the monomethyl ester of the triphosphate using the Sybyl

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2

Bazarova, E. A. "Study of complexing properties of mono-derivatives of alkenyl succinic acid with copper(II) and nickel(II) ions." Transaction Kola Science Centre 11, no. 3-2020 (2020): 10–15. http://dx.doi.org/10.37614/2307-5252.2020.3.4.001.

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Mono-derivatives of alkenyl succinic acid are considered in this paper, also their complexes with copper and nickel ions, which structure was studied by IR spectrometry method. Protonization constants and stability constants of complexes of mono-derivatives of succinic acid with copper and nickel ions are calculated by pH-metric titration method. It has been established, that mono-derivatives of succinic acid formed more stable complexes with the copper ion.

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3

Kvaratskhelia, E., and R. Kurtanidze. "PECULIARITIES OF ELECTROLYTIC DISSOCIATION OF ETHYL DERIVATIVES OF SUCCINIC ACID." Chemical Problems 2018, no. 1 (2018): 63–68. http://dx.doi.org/10.32737/2221-8688-2018-1-63-68.

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4

Ravindra, S. Dhivare, and S. Rajput Shankarsing. "SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF FIVE MEMBERED CYCLIC IMIDE DERIVATIVES OF MONO, DI AND TRI SUBSTITUTED AROMATIC AMINES AND NAPTHYL AMINE." World Journal of Pharmaceutical Research 4, no. 6 (2019): 1650–58. https://doi.org/10.20959/wjpr20156-3632.

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The five-membered cyclic imide derivatives were prepared by reacting succinic anhydride with substituted aromatic amines and naphthyl amine to get 3-(N-phenyl carbamoyl) propanoic acid and 3-(N-napthylcarbamoyl) propanoic acid. These intermediates underwent ring closer with acetyl chloride furnished five-membered cyclic imides derivatives. All these derivatives were screened for antimicrobial activities.

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5

Lyakhov, Alexander S., Ludmila S. Ivashkevich, Vladimir L. Survilo, and Tatjana V. Trukhachova. "Two succinic acid derivatives of 2-ethyl-6-methylpyridin-3-ol." Acta Crystallographica Section C Crystal Structure Communications 68, no. 1 (2011): o33—o36. http://dx.doi.org/10.1107/s0108270111054692.

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Crystals of bis(2-ethyl-3-hydroxy-6-methylpyridinium) succinate–succinic acid (1/1), C8H12NO+·0.5C4H4O42−·0.5C4H6O4, (I), and 2-ethyl-3-hydroxy-6-methylpyridinium hydrogen succinate, C8H12NO+·C4H5O4−, (II), were obtained by reaction of 2-ethyl-6-methylpyridin-3-ol with succinic acid. The succinate anion and succinic acid molecule in (I) are located about centres of inversion. Intermolecular O—H...O, N—H...O and C—H...O hydrogen bonds are responsible for the formation of a three-dimensional network in the crystal structure of (I) and a two-dimensional network in the crystal structure of (II). B

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6

Annweiler, Eva, Arne Materna, Michael Safinowski, et al. "Anaerobic Degradation of 2-Methylnaphthalene by a Sulfate-Reducing Enrichment Culture." Applied and Environmental Microbiology 66, no. 12 (2000): 5329–33. http://dx.doi.org/10.1128/aem.66.12.5329-5333.2000.

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ABSTRACT Anaerobic degradation of 2-methylnaphthalene was investigated with a sulfate-reducing enrichment culture. Metabolite analyses revealed two groups of degradation products. The first group comprised two succinic acid adducts which were identified as naphthyl-2-methyl-succinic acid and naphthyl-2-methylene-succinic acid by comparison with chemically synthesized reference compounds. Naphthyl-2-methyl-succinic acid accumulated to 0.5 μM in culture supernatants. Production of naphthyl-2-methyl-succinic acid was analyzed in enzyme assays with dense cell suspensions. The conversion of 2-methy

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7

Pozdnyakov, Dmitry I., Denis S. Zolotych, and Michael V. Larsky. "Correction of mitochondrial dysfunction by succinic acid derivatives under experimental cerebral ischemia conditions." Current Issues in Pharmacy and Medical Sciences 34, no. 1 (2021): 42–48. http://dx.doi.org/10.2478/cipms-2021-0008.

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Abstract The aim of the study. To evaluate the effect of succinic acid derivatives on changes of mitochondrial function in rats under cerebral ischemia conditions. Materials and methods. In this work, the effect of succinic acid, ethylmethylhydroxypyridine succinate, and acetylaminosuccinic acid at doses of 50 mg/kg, 100 mg/kg, and 200 mg/kg (per os) on the change of the neuronal mitochondria function was studied. Cerebral ischemia was reproduced by the Tamura method. The following parameters were evaluated: changes in aerobic/anaerobic metabolism, mitochondrial membrane potential, the opening

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8

Mitrofanova, G. V., and V. A. Ivanova. "Surface-active properties of succinic acid monoalkyl derivatives." Russian Journal of Applied Chemistry 84, no. 3 (2011): 361–67. http://dx.doi.org/10.1134/s1070427211030049.

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9

Bubnov, Yu N., A. A. Prishchenko, M. V. Livantsov, O. P. Novikova, L. I. Livantsova, and S. V. Baranin. "Synthesis of functionalized organophosphorus derivatives of succinic acid." Russian Chemical Bulletin 73, no. 8 (2024): 2339–49. http://dx.doi.org/10.1007/s11172-024-4358-8.

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10

Pizova, Natalia Vyacheslavovna. "SUCCINIC ACID DERIVATIVES IN THERAPY FOR CEREBROVASCULAR DISEASE." Neurology, neuropsychiatry, Psychosomatics, no. 1 (March 14, 2010): 67. http://dx.doi.org/10.14412/2074-2711-2010-74.

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11

XU, JINGYUAN, VEERA M. BODDU, and SEAN X. LIU. "RHEOLOGICAL PROPERTIES OF HYDROGELS PRODUCED BY CELLULOSE DERIVATIVES CROSSLINKED WITH CITRIC ACID, SUCCINIC ACID AND SEBACIC ACID." Cellulose Chemistry and Technology 56, no. 1-2 (2022): 49–54. http://dx.doi.org/10.35812/cellulosechemtechnol.2022.56.04.

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"Cellulose is the most abundant biopolymer in our world, and a natural, biodegradable and inexpensive resource for biomaterials. This work prepared cellulose-based hydrogels by cross-linking cellulose derivatives using citric acid, succinic acid, and sebacic acid, and explored the rheological properties of the three cellulose-based hydrogels. We found that the viscoelastic properties of this kind of cellulose-based biodegradable hydrogels can be manipulated by hydrogel concentration and using the three different cross-linkers. The cellulose-based hydrogels cross-linked with citric acid (CHCCA)

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12

Li, Tang-ming, Jing-hua Han, Bing-qian Hu, Fan Yu, and Bao Li. "A highly active oxygen evolution electrocatalyst derived from Co/Ni-succinic acid framework under mild conditions." CrystEngComm 24, no. 7 (2022): 1453–58. http://dx.doi.org/10.1039/d1ce01636a.

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13

Palagina, I. A. "Pro-/antioxidant reactions and nitrogen oxide metabolism under sub-chronic effect of succinic acid derivatives." Ukrainian Biochemical Journal 89, no. 4 (2017): 22–33. http://dx.doi.org/10.15407/ubj89.04.022.

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14

Allan, RD, and C. Apostopoulos. "Synthesis of Substituted (+)-Bicuculline Derivatives Through Chloromethylation." Australian Journal of Chemistry 43, no. 7 (1990): 1259. http://dx.doi.org/10.1071/ch9901259.

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Treatment of the phthalide isoquinoline alkaloid (+)- bicuculline with paraformaldehyde and hydrochloric acid leads to the chloromethyl derivative (4) which can be further substituted with ammonia or piperazine . In reactions to study methods of linking bicuculline to macromolecules or to photolabile groups, the amino product (7a) has been further functionalized by the formation of amide linkages with succinic anhydride and 4-aminobenzoic acid.

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15

Kvaratskhelia, Elene, and Rusudan Kurtanidze. "The Electrolytic Dissociation of Aryl Derivatives of Succinic Acid." Journal of Biomedical Science and Engineering 10, no. 04 (2017): 163–71. http://dx.doi.org/10.4236/jbise.2017.104013.

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16

Menger, F. M., and L. H. Lee. "Conformation of succinic acid derivatives by double 13C-labelling." Tetrahedron Letters 29, no. 7 (1988): 757–60. http://dx.doi.org/10.1016/s0040-4039(00)80202-6.

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17

Wirz, Beat, and Milan Soukup. "Enzymatic preparation of homochiral 2-isobutyl succinic acid derivatives." Tetrahedron: Asymmetry 8, no. 2 (1997): 187–89. http://dx.doi.org/10.1016/s0957-4166(96)00515-0.

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18

Flores-Sandoval, C. A., I. P. Zaragoza, V. F. Marañón-Ruiz, J. Correa-Basurto, and J. Trujillo-Ferrara. "Theoretical study of aryl succinic and maleic acid derivatives." Journal of Molecular Structure: THEOCHEM 713, no. 1-3 (2005): 127–34. http://dx.doi.org/10.1016/j.theochem.2004.11.004.

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19

Loginova, E. S., V. M. Nikol´skii, L. N. Tolkacheva, and N. I. Luk´yanova. "Synthesis and some properties of complexones, succinic acid derivatives." Russian Chemical Bulletin 65, no. 9 (2016): 2206–10. http://dx.doi.org/10.1007/s11172-016-1569-7.

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20

Luo, Xuzhong, Wei Xiao, Zengfu Li, Qiong Wang, and Jinlian Zhong. "Supramolecular organogels formed by monochain derivatives of succinic acid." Journal of Colloid and Interface Science 329, no. 2 (2009): 372–75. http://dx.doi.org/10.1016/j.jcis.2008.10.013.

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21

Lozano-Montante, Jorge, Raquel Garza-Hernández, Mario Sánchez, et al. "Chitosan Functionalized with 2-Methylpyridine Cross-Linker Cellulose to Adsorb Pb(II) from Water." Polymers 13, no. 18 (2021): 3166. http://dx.doi.org/10.3390/polym13183166.

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In this study, chitosan was chemically modified with 2-methylpyridine. Subsequently, the modified chitosan was cross-linked to cellulose using succinic anhydride. Additionally, the capacity of cellulose derivatives to adsorb Pb(II) ions in an aqueous solution was studied through the determination of Pb(II) ions concentration in water, using microwave plasma atomic emission spectroscopy (MP-AES). A maximum adsorption capacity of 6.62, 43.14, 60.6, and 80.26 mg/g was found for cellulose, cellulose-succinic acid, cellulose-chitosan, and cellulose-chitosan-pyridine, respectively. The kinetic data

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22

Bohdan, Anna, Yanina Romanenko, Mikhail Zavhorodnii, et al. "Design, Synthesis and Biological Activity of the 4-Thioquinoline Derivative." Chemistry & Chemical Technology 17, no. 4 (2023): 774–85. http://dx.doi.org/10.23939/chcht17.04.774.

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One of the promising areas in the creation of bioregulators is the modeling of compounds that combine several pharmacophores. The design of new highly efficient and low-toxic cytoprotectors is largely based on the derivatives of nitrogen-containing heterocycles, and quinoline plays a significant role among these compounds. The researchers evaluated the toxicity of the tested compounds in silico, in vitro, and in vivo, which allowed determiningseveral factors that affect the level of toxic action of 4-thioquinoline derivatives and the direction of non-toxic substances in this sequence. The stud

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23

Hu, Jianxiang, Lisha Zhao, Shuangqing Liu, and Yanhua Cai. "Synthesis and Performances of Hydrocinnamic Acid Derivatives Containing Alkyl Dihydrazide." E3S Web of Conferences 261 (2021): 02023. http://dx.doi.org/10.1051/e3sconf/202126102023.

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In this work, four hydrocinnamic acid derivatives including N, N’-succinic bis(hydrocinnamic acid) dihydrazide (HASUD), N, N’-adipic bis(hydrocinnamic acid) dihydrazide (HAADD), N, N’-sebacic bis(hydrocinnamic acid) dihydrazide (HASED) and N, N’-dodecanedioic bis(hydrocinnamic acid) dihydrazide (HADOD) were synthesized via two liquid reactions. And then fourier transform infrared spectrometer and 1H nuclear magnetic resonance were used to characterize molecular structures of four hydrocinnamic acid derivatives. Additionally, the orthogonal experiment obtained the optimum synthesis process of f

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24

Bailey, Murray D., Ted Halmos, Dan Adamson, Josée Bordeleau, and Chantal Grand-Maı̂tre. "Chemo-enzymatic synthesis of chiral 2-substituted succinic acid derivatives." Tetrahedron: Asymmetry 10, no. 17 (1999): 3285–95. http://dx.doi.org/10.1016/s0957-4166(99)00330-4.

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25

Gulevich, A. Yu, A. Yu Skorokhodova та V. G. Debabov. "Effect of the Glyoxylate Shunt Inactivation on Biosynthesis of Adipic Acid Through the Inverted Fatty Acid β-oxidation by <i>Escherichia coli</i> Strains". Прикладная биохимия и микробиология 59, № 3 (2023): 235–43. http://dx.doi.org/10.31857/s055510992303008x.

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Using Escherichia coli MG1655 lacIQ, ∆ackA-pta, ∆poxB, ∆ldhA, ∆adhE, ∆fadE, PL-SDφ10-atoB, Ptrc-ideal-4-SDφ10-fadB, PL-SDφ10-tesB, ∆yciA as a core strain, the derivatives capable of synthesizing adipic acid from glucose through the inverted fatty acid β-oxidation pathway were obtained. Biosynthesis of the target compound by recombinants was ensured upon the primary condensation of acetyl-CoA and succinyl-CoA by 3-oxoacyl-CoA thiolase PaaJ and the catalysis of the final reaction of the cycle by acyl-CoA dehydrogenases FadE and FabI. Deletion in the strains of sucCD genes encoding components of

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26

Voronkov, Andrey V., Dmitry I. Pozdnyakov, Similla L. Adjiahmetova, Nadezhda M. Chervonnaya, Victoria M. Rukovitsina, and Eduard "T" Oganesyan. "Influence of some cinnamic acid derivatives on changes of the tricarboxylic acid cycle enzymes activity in rats under brain ischemia conditions." Medical academic journal 20, no. 2 (2020): 27–32. http://dx.doi.org/10.17816/maj33994.

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The aim of the study was to assess the effect of certain derivatives of cinnamic acids on changes of the tricarboxylic acid cycle enzymes activity under experimental cerebral ischemia. Materials and methods. Brain ischemia was modeled by irreversible right-sided coagulation of the middle cerebral artery. Test compounds: 4-hydroxy-3,5-ditretbutyl cinnamic acid, coumaric, coffee, synapic, cinnamic, 4-hydroxycinnamic and ferulic acids, as well as a reference drug succinic acid was administered at a dose of 100 mg / kg per os for 3 days after the reproduction of ischemia. Then, changes in th

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27

Rusul Ali Muhammad and Rajaa A. A. Ghafil. "Synthesis, Identification some of new heterocyclic Compounds Derivatives and study of the biological Activity." Journal of Kufa for Chemical Sciences 3, no. 3 (2024): 336–51. https://doi.org/10.36329/jkcm/2024/v3.i3.15932.

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This research includes prepeared of some new heterocyclic compounds from 2-hydroxy napthaldehyde with 2-amino thiazol , 2-amino thiazol reacted with 2-hydroxy napthaldehyde , to produce shiff base derivative (R),(R) using to synthesis of some new heterocyclic derivatives by reactions and reactant with types solvent and materials to synthesis heterocyclic membered ring , first step : Involved synthesis of seven heterocyclic compounds by reacting (R) with phthalic ,succinic and malic anhydride respectfully to prepeared oxazepine compounds (R1,R2,R3) . Second step involves preparing of five- hete

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28

Brown, Samantha J., Stuart Corr, and Jonathan M. Percy. "Fluorinated succinic acid derivatives from new refrigerants via ozonolysis of haloalkenes." Tetrahedron Letters 41, no. 27 (2000): 5269–73. http://dx.doi.org/10.1016/s0040-4039(00)00804-2.

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29

Raya, J. Espinosa, J. Correa-Basurto, J. I. Vázquez Alcántara, and J. G. Trujillo-Ferrara. "(17) Effects of succinic acid derivatives on ex vivo acetylcholinesterase activity." Chemico-Biological Interactions 157-158 (December 2005): 379–80. http://dx.doi.org/10.1016/j.cbi.2005.10.062.

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30

Yoon, Seung-Bin, Jae-Sung Yang, Kyung-Ho Lee, Hyeon-Gyu Han, Ah-Reum Han, and Young-Sook Paik. "Synthesis and evaluation of succinic acid derivatives as prolyl endopeptidase inhibitors." Journal of the Korean Society for Applied Biological Chemistry 54, no. 5 (2011): 731–37. http://dx.doi.org/10.1007/bf03253152.

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31

Volchegorskii, I. A., I. Yu Miroshnichenko, L. M. Rassokhina, et al. "Antidepressant effect of 3-oxypyridine and succinic acid derivatives (experimental study)." Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova 115, no. 2 (2015): 48. http://dx.doi.org/10.17116/jnevro20151152148-52.

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32

UCHIDA, Takuya, Yasuyuki ENDO, Shoji HIZATATE, and Koichi SHUDO. "Anionic hetero(3,3)rearrangements. N,O-diacylhydroxylamines to succinic acid derivatives." CHEMICAL & PHARMACEUTICAL BULLETIN 42, no. 2 (1994): 419–21. http://dx.doi.org/10.1248/cpb.42.419.

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33

Bailey, Murray D., Ted Halmos, Dan Adamson, Josee Bordeleau, and Chantal Grand-Maitre. "ChemInform Abstract: Chemoenzymatic Synthesis of Chiral 2-Substituted Succinic Acid Derivatives." ChemInform 31, no. 3 (2010): no. http://dx.doi.org/10.1002/chin.200003083.

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34

WIRZ, B., and M. SOUKUP. "ChemInform Abstract: Enzymatic Preparation of Homochiral 2-Isobutyl Succinic Acid Derivatives." ChemInform 28, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.199722038.

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35

YAMAGUCHI, Toshiaki, Takashi YANAGI, Hiroshi HOKARI, Yuko MUKAIYAMA, Tetsuhide KAMIJO, and Iwao YAMAMOTO. "Preparation of Optically Active Succinic Acid Derivatives. III. Regioselective Condensation Reactions of Optically Active 2-Substituted Succinic Acids with Diimidazolide." YAKUGAKU ZASSHI 118, no. 6 (1998): 248–55. http://dx.doi.org/10.1248/yakushi1947.118.6_248.

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36

Hadizadeh, Farzin, Alireza Moradi, Goli Naghibi, Mojgan Vojdani, Javad Behravan, and Mohammad Ramezani. "Synthesis and Antitumor Activity of Substituted Succinamides Using a Potato Disc Tumor Induction Assay." International Journal of Biomedical Science 3, no. 1 (2007): 60–64. http://dx.doi.org/10.59566/ijbs.2007.3060.

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In view of potential biological activities of some succinic acid derivatives, we synthesized some novel N-[4-(4-morpholinosulfonyl)-phenyl]-succinamides (6a, c; 7a, c) and N-[4-(benzylaminosulfonyl) phenyl]-succinamides (6b, d; 7b, d) derivatives as antitumor agents. The antitumor activity of compounds was studied using the potato disk bioassay technique (Figure 1). Vincristine at 0.25mg/ml was employed as positive control and caused -67.24% inhibitions. Compound 7b at 1 mg/ml caused -80.50% tumor inhibitions with highest activity among compounds tested.

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37

T., SAROJINI, C. SOMASEKHARA REDDY M., and RAMACHANDRAIAH A. "Electrochemical Characteristics of N-Phenylmonoamide Derivatives of some 1,2-Dicarboxylic Acids." Journal of Indian Chemical Society Vol. 72, Jan 1995 (1995): 33–36. https://doi.org/10.5281/zenodo.5900449.

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Department of Chemistry, Regional Engineering College, Warangal-506 004 Department of Chemistry, G. Pulla Reddy Engineering College, Pulla Reddy Nagar, Kurnool-518 002 <em>Manuscript received 16 December 1992, revised 9 June 1993, accepted 12 October 1993</em> Electrochemical investigations have been carried out on a few NaL systems by cyclic voltammetric and coulometric techniques, where HL' s are N-phenylmonoamide derivatives of 1,2-dicarboxylic acids (1), on mercury electrode in a buffered aqueous media (pH range 6-12) at room temperature (25°). Only the maleic acid derivatives resp

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38

Burdzhiev, Nikola T., and Elena R. Stanoeva. "Synthesis of New Polysubstituted Pyrrolidinones with Potential Biological Activity." Zeitschrift für Naturforschung B 63, no. 3 (2008): 313–20. http://dx.doi.org/10.1515/znb-2008-0315.

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The reaction of succinic anhydride and N-benzylidene-benzylamine gave rise to the corresponding substituted trans-5-oxopyrrolidine-3-carboxylic acid, which was transformed stereoselectively into two series of compounds. The first one consists of carboxamides, and the second one includes aminomethyl derivatives. The compounds prepared incorporate both a pyrrolidinone part and other nitrogen containing heterocyclic fragments of pharmacological interest.

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39

El-Shaieb, Kamal M. "Synthesis of 4-arylaminoquinazoline-2-carboxylic acid derivatives by the reaction of (Z)-2-amino-N′-aryl-benzimidamides with some selected anhydrides." Zeitschrift für Naturforschung B 74, no. 7-8 (2019): 603–6. http://dx.doi.org/10.1515/znb-2019-0086.

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AbstractNovel reactions of (Z)-2-amino-N′-arylbenzimidamides (1a, b) are described. When 1a, b are reacted with diphenic, phthalic and succinic anhydrides, in dry ethyl alcohol under reflux conditions, the 4-arylaminoquinazoline-2-carboxylic acid derivatives (3a–f) were formed in good yields. The structures of the products were assigned on the basis of their spectroscopic and analytical data.

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40

Luo, Qi, Yan-Jiao Zhang, Zhi-Qiang Shen, Peng Chen, and Yong-Xian Cheng. "Shushe Acids A-D from Ganoderma Applanatum." Natural Product Communications 12, no. 3 (2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200321.

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Ganoderma applanatum is a fungus used for the prevention and treatment of a variety of disorders in China. In the present study, four new compounds, named shushe acids A-D (1-4), were isolated from the fruiting bodies of this species. Their structures were identified on the basis of spectroscopic methods. Compounds 1-4 are all natural product hybrids composed of derivatives of gallic acid, glycerol and succinic acid. None of the four compounds showed activity against the MCF-7 cell line.

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41

Banjac, Nebojsa, Nemanja Trisovic, Natasa Valentic, Gordana Uscumlic, and Slobodan Petrovic. "Succinimides: Synthesis, properties and anticonvulsant activity." Chemical Industry 65, no. 4 (2011): 439–53. http://dx.doi.org/10.2298/hemind110224030b.

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Succinimide is a cycle imide of succinic acid that is present in numerous biologically active compounds including anticonvulsants, antitremor, anti-Parkinson`s agents. This paper describes different ways of synthesis of succinimide-derivatives their physical properties and reactivity. Also, the most widely used succinimide anticonvulsants and the analysis of structure-activity relationships of anticonvulsant drugs in terms of lipophilicity and hydrogen bonding are presented here.

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42

Xu, Chao, Md Asraful Alam, Jun Zhang, et al. "Identification of lignocellulosic derivatives inhibiting succinic acid fermentation and molecular mechanism investigation." Industrial Crops and Products 187 (November 2022): 115466. http://dx.doi.org/10.1016/j.indcrop.2022.115466.

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43

Baek, Seung-Yeob, Young-Wun Kim, Keunwoo Chung, Seung-Hyun Yoo, Nam Kyun Kim, and Yeong-Joon Kim. "Synthesis of Succinic Acid Alkyl Half-Ester Derivatives with Improved Lubricity Characteristics." Industrial & Engineering Chemistry Research 51, no. 9 (2012): 3564–68. http://dx.doi.org/10.1021/ie202137r.

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44

Makurina, V. I., V. P. Chernykh, I. S. Gritsenko, et al. "Correlations of structure and activity for derivatives of arenesulfohydrazides of succinic acid." Pharmaceutical Chemistry Journal 20, no. 9 (1986): 665–69. http://dx.doi.org/10.1007/bf01148645.

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45

Kim, Ji Yeon, Jong An Lee, and Sang Yup Lee. "Biobased Production of Succinic Acid and Its Derivatives Using Metabolically Engineered Microorganisms." Industrial Biotechnology 19, no. 3 (2023): 125–37. http://dx.doi.org/10.1089/ind.2023.0001.

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46

Смирнова, Татьяна Ивановна, Ирина Геннадьевна Тумасьева, Людмила Николаевна Толкачева, and Виктор Михайлович Никольский. "EFFECT OF COMPLEXONS, DERIVATIVES OF SUCCINIC ACID, ON THE FORMATION OF CAROTENOIDS IN GREEN PLANTS." Вестник Тверского государственного университета. Серия: Химия, no. 3(45) (October 18, 2021): 175–81. http://dx.doi.org/10.26456/vtchem2021.3.19.

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На основании обобщения результатов многолетних лабораторных и полевых опытов обнаружена зависимость уровня содержания жёлтых фотосинтетических пигментов в растениях от внекорневой обработки растворами комплексонов. Комплексоны, производные янтарной кислоты (иминодиянтарная кислота, этилендиаминдиянтарная кислота, диаминоциклогександиянтарная кислота) способствуют накоплению каротиноидов в зелёных растениях, а этилендиаминтетрауксусная кислота существенно не влияет на их содержание. Based on the generalization of the results of many years of laboratory and field experiments, the dependence of t

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Smirnova, T. I., I. A. Drozdov, and M. N. Pavlov. "The Study of Degradation of Complexones, Derivatives of Succinic Acid, and their Boron-Containing Complexes Under the Influence of Microbiological Preparations." Ecology and Industry of Russia 25, no. 6 (2021): 49–53. http://dx.doi.org/10.18412/1816-0395-2021-6-49-53.

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The results of the study of the possibility of degradation of complexones, derivatives of succinic acid (CDSA), iminodisuccinic acid (IDSA), ethylenediaminedisuccinic acid (EDCSA), trans-1, 2-diaminocyclohexanedisuccinic acid (DCHDSA) and complexones taken for comparison, derivatives of iminodiacetic acid (IDSA) and ethylenediaminetetraacetic acid (EDTAA) under the influence of microbiological preparations “Baikal EM-1” and “Rhizoplane L”, as well as borate complexes of CDSA: B-IDSA, B-EDCSA and B-DCHDSA under the influence of the preparation Rhizoplane L at a temperature 22±1oC in an aqueous

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Adil, Husham, and Nabeel Y. J. Al-Hiti. "Synthesis and Characterization of 1,3-Oxazepindion Derivatives via Diformylbenzene Imines as Precursors." Samarra Journal of Pure and Applied Science 6, no. 2 (2024): 1–16. http://dx.doi.org/10.54153/sjpas.2024.v6i2.631.

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In this paper, 1,3-oxazepindione derivatives [D] and [E] were prepared by reacting Schiff bases di Azomethine [A], [B], and [C] with maleic anhydride and succinic anhydride in the presence of dried benzene as a solvent. Schiff bases di Azomethine [A], [B], and [C] were prepared by reacting Terephthalaldehyde, Isophthalaldehyde, or o-Phthalaldehyde with 5 drops of glacial acetic acid as a catalyst and halo-aniline derivatives in absolute ethanol as a solvent. The prepared compounds were diagnosed and confirmed by using infrared and nuclear magnetic resonance spectroscopies. All the reactions of

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Jiang, Rui-Jian, Bo Yang, Dong Yi та ін. "Synthesis and characterization of a series of novel amino β-cyclodextrin-conjugated poly(ε-lysine) derivatives". Journal of Polymer Engineering 34, № 2 (2014): 133–39. http://dx.doi.org/10.1515/polyeng-2013-0194.

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Abstract Soluble poly(ε-lysine)s bearing β-cyclodextrin (β-CD) moieties were prepared by three amino β-CD derivatives and N-succinylated poly(ε-lysine), in which the poly(ε-lysine) and amino β-CD derivatives were bonded covalently to the end carboxyl groups of succinic acid by peptide bonds. 1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDCI) and N-hydroxysuccinimide (NHS) were chosen to assist the reaction. The three poly(ε-lysine) derivatives were characterized by 1H nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FT-IR). The synthesis process is simple, f

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Amin, M. A., H. Shokry, and E. M. Mabrouk. "Nickel Corrosion Inhibition in Sulfuric Acid—Electrochemical Studies, Morphologies, and Theoretical Approach." Corrosion 68, no. 8 (2012): 699–712. http://dx.doi.org/10.5006/0508.

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The inhibition performance of three selected dihydrazide derivatives, namely, malonic acid (MAD), succinic acid (SAD), and adipic acid (AAD) dihydrazide, was tested in relation to nickel corrosion in 1.0 M sulfuric acid (H2SO4) solution. Electrochemical methods (Tafel polarization, linear polarization resistance [LPR], and electrochemical impedance spectroscopy [EIS]) were used, complemented with scanning electron microscopy/energy-dispersive x-ray (SEM/EDX) examinations. Computational studies were also used to confirm experimental findings and to optimize the adsorption structures of dihydraz

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