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Journal articles on the topic 'Dimethyl succinate'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Daviot, Laura, Thomas Len, Carol Lin, and Christophe Len. "Microwave-Assisted Homogeneous Acid Catalysis and Chemoenzymatic Synthesis of Dialkyl Succinate in a Flow Reactor." Catalysts 9, no. 3 (2019): 272. http://dx.doi.org/10.3390/catal9030272.

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Two new continuous flow systems for the production of dialkyl succinates were developed via the esterification of succinic acid, and via the trans-esterification of dimethyl succinate. The first microwave-assisted continuous esterification of succinic acid with H2SO4 as a chemical homogeneous catalyst was successfully achieved via a single pass (ca 320 s) at 65–115 °C using a MiniFlow 200ss Sairem Technology. The first continuous trans-esterification of dimethyl succinate with lipase Cal B as an enzymatic catalyst was developed using a Syrris Asia Technology, with an optimal reaction condition

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2

Yang, Yongqiang, Ruyue Shao, Li Tang, et al. "Succinate dehydrogenase inhibitor dimethyl malonate alleviates LPS/d-galactosamine-induced acute hepatic damage in mice." Innate Immunity 25, no. 8 (2019): 522–29. http://dx.doi.org/10.1177/1753425919873042.

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In addition to its energy-supplying function, increasing evidence suggests that mitochondria also play crucial roles in the regulation of inflammation. Succinate dehydrogenase is also known as mitochondrial complex II, and inhibition of succinate dehydrogenase by dimethyl malonate has been reported to suppress the production of pro-inflammatory cytokines. In the present study, the potential anti-inflammatory benefits of dimethyl malonate were investigated in a mouse model with LPS/d-galactosamine-induced acute hepatic damage. Male BALB/c mice were injected i.p. with LPS and d-galactosamine to

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3

Malaisse, W. J., and A. Sener. "Metabolic effects and fate of succinate esters in pancreatic islets." American Journal of Physiology-Endocrinology and Metabolism 264, no. 3 (1993): E434—E440. http://dx.doi.org/10.1152/ajpendo.1993.264.3.e434.

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The metabolic effects and the catabolism of succinate methyl esters were examined in rat pancreatic islets. The esters augmented 14CO2 production from islets prelabeled with L-[U-14C]-glutamine but inhibited NH4+ output, suggesting that they do not activate glutamate dehydrogenase. They decreased 14CO2 output from islets prelabeled with [U-14C]palmitate. They had little effect on the oxidation of exogenous D-[3,4-14C]glucose, D-[2-14C]glucose, D-[6-14C]glucose, or D-[1-14C]glucose, suggesting unaltered ratio between the input of acetyl residues and four- or five-carbon metabolites, such as suc

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4

Tryznowski, M., A. Świderska, T. Gołofit, and Z. Żołek-Tryznowska. "Wood adhesive application of poly(hydroxyurethane)s synthesized with a dimethyl succinate-based amide backbone." RSC Advances 7, no. 48 (2017): 30385–91. http://dx.doi.org/10.1039/c7ra05455f.

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5

Cybulski, Andrzej, Jerzy Chrząszcz, and Martyn V. Twigg. "Hydrogenation of dimethyl succinate over monolithic catalysts." Catalysis Today 69, no. 1-4 (2001): 241–45. http://dx.doi.org/10.1016/s0920-5861(01)00375-3.

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6

Turek, T., D. L. Trimm, D. StC Black, and N. W. Cant. "Hydrogenolysis of dimethyl succinate on copperbased catalysts." Applied Catalysis A: General 116, no. 1-2 (1994): 137–50. http://dx.doi.org/10.1016/0926-860x(94)80285-8.

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7

Du, Chengzhe, Chenghao Zhao, Huixia Ma, Rui Jiang, Huanling Zhang та Feng Zhou. "Kinetic study on the hydrogenation of dimethyl succinate to γ-butyrolactone". RSC Advances 15, № 18 (2025): 14307–14. https://doi.org/10.1039/d5ra01226k.

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The intrinsic reaction pathway for the hydrogenation of dimethyl succinate to γ-butyrolactone using the CuZnAl catalyst is proposed, and the comparison between experimental values and fitted values highlights the accuracy of the model.

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8

Choudhury, Streeti R., James A. Traquair, and William R. Jarvis. "New extracellular fatty acids in culture filtrates of Sporothrixflocculosa and S. rugulosa." Canadian Journal of Chemistry 73, no. 1 (1995): 84–87. http://dx.doi.org/10.1139/v95-012.

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Two new and rare unsaturated, extracellular fatty acids were identified in the culture filtrates of the biocontrol fungi, Sporothrixflocculosa and S. rugulosa. 16-Methyl-9E-nonadecenoic acid (1) and (Z,Z)-10,14-eicosadienoic acid (2) were characterized on the basis of infrared (IR) and nuclear magnetic resonance spectra (13C and 1N NMR), and gas chromatographic – mass spectrometric data (GC–MS). The structure of compounds 1 and 2 was confirmed by oxidative degradation to the known standards, dimethyl azelate, dimethyl succinate, dimethyl sebacate, and methyl caproate. Keywords: unsaturated fat

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9

Emtiazi, Hamideh, and Mohammad Ali Amrollahi. "An Efficient Isocyanide-Based Three-Component Synthesis of Novel Ketenimines." JOURNAL OF ADVANCES IN CHEMISTRY 10, no. 3 (2014): 2363–68. http://dx.doi.org/10.24297/jac.v10i3.2286.

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This study provides a description of an efficient and simple procedure for the synthesis of dimethyl 2-(9-aryl)-3,3,6,6-tetramethyl-1,8-diox-1,2,3,4,5,6,7,8-octahydroacridin-10(9H)-yl)-3-((cyclohexylimino)methylene)succinate via a one-pot three-component reaction of cyclohexyl isocyanide, dimethyl acetylenedicarboxylate and hexahydroacridine-1,8(2H,5H)-dionesin CH2Cl2 at room temperature. Short reaction times, good to high yields and the novelty are the remarkable advantages of this work.

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10

Yadav, Hanuman Singh, and Saba Gani. "Antioxident Activity of Greenly Synthesized Anhydride." International Journal of Trend in Scientific Research and Development 2, no. 1 (2017): 310–15. https://doi.org/10.31142/ijtsrd5847.

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One pot synthesis of acid esters by Stobbe condensation of alkylidene arylidene succinates and aldehydes or ketones, their subsequent hydrolysis to diacids hasreported. TheStobbe condensation of various aromatic aldehydes or ketones with dimethyl succinate gives different types of cyclized productsthrough green approach. The improved yields of Fulgenic acid and its anhydridehave observed by the green approach method as compared with other classical methods employed so far.The antioxidant activity of anhydride compounds have done by using DPPH. Yadav Hanuman Singh | Gani Saba "Antioxident

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11

López-Garzón, Camilo S., Luuk A. M. van der Wielen, and Adrie J. J. Straathof. "Ester production from bio-based dicarboxylates via direct downstream catalysis: succinate and 2,5-furandicarboxylate dimethyl esters." RSC Advances 6, no. 5 (2016): 3823–29. http://dx.doi.org/10.1039/c5ra17752a.

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Two culture broths, one containing succinate produced de novo by C. glutamicum and the other containing 2,5-furandicarboxylate produced by whole cell biotransformation of 5-HMF by a recombinant P. putida, were used for dimethyl ester production.

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12

Zaunmüller, Tanja, David J. Kelly, Frank O. Glöckner, and Gottfried Unden. "Succinate dehydrogenase functioning by a reverse redox loop mechanism and fumarate reductase in sulphate-reducing bacteria." Microbiology 152, no. 8 (2006): 2443–53. http://dx.doi.org/10.1099/mic.0.28849-0.

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Sulphate- or sulphur-reducing bacteria with known or draft genome sequences (Desulfovibrio vulgaris, Desulfovibrio desulfuricans G20, Desulfobacterium autotrophicum [draft], Desulfotalea psychrophila and Geobacter sulfurreducens) all contain sdhCAB or frdCAB gene clusters encoding succinate : quinone oxidoreductases. frdD or sdhD genes are missing. The presence and function of succinate dehydrogenase versus fumarate reductase was studied. Desulfovibrio desulfuricans (strain Essex 6) grew by fumarate respiration or by fumarate disproportionation, and contained fumarate reductase activity. Desul

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13

Koivunen, Peppi, Maija Hirsilä, Anne M. Remes, Ilmo E. Hassinen, Kari I. Kivirikko, and Johanna Myllyharju. "Inhibition of Hypoxia-inducible Factor (HIF) Hydroxylases by Citric Acid Cycle Intermediates." Journal of Biological Chemistry 282, no. 7 (2006): 4524–32. http://dx.doi.org/10.1074/jbc.m610415200.

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The stability and transcriptional activity of the hypoxia-inducible factors (HIFs) are regulated by two oxygen-dependent events that are catalyzed by three HIF prolyl 4-hydroxylases (HIF-P4Hs) and one HIF asparaginyl hydroxylase (FIH). We have studied possible links between metabolic pathways and HIF hydroxylases by analyzing the abilities of citric acid cycle intermediates to inhibit purified human HIF-P4Hs and FIH. Fumarate and succinate were identified as in vitro inhibitors of all three HIF-P4Hs, fumarate having Ki values of 50–80 μm and succinate 350–460 μm, whereas neither inhibited FIH.

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14

İnce, Erol, and Ş. İsmail Kırbaşlar. "Liquid–Liquid Equilibria of Water + Ethanol + Dibasic Esters Mixture (Dimethyl Adipate + Dimethyl Glutarate + Dimethyl Succinate) Ternary System." Separation Science and Technology 39, no. 13 (2004): 3151–62. http://dx.doi.org/10.1081/ss-200028823.

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15

Mazur, H., V. Merlavsky, B. O. Manko, and V. V. Manko. "Dependence of the adaptive capacity of liver mitochondria on preparation method." Visnyk of Lviv University. Biological series, no. 82 (November 3, 2020): 177–85. http://dx.doi.org/10.30970/vlubs.2020.82.16.

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When conducting studies on isolated hepatocytes, it is important to obtain cells that retain the functional properties that are characteristic of the whole organ. Increased blood viscosity during liver perfusion, decreased perfusion pressure in blood vessels, and hence hypoxia, are among the factors that may affect the functional state of isolated hepatocytes. The functional state of cells can be estimated by the adaptive capacity of mitochondria, by inducing maximal respiration rate by uncoupling respiration and oxidative phosphorylation due to the addition of FCCP. The research aimed to inve

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16

MacDonald, Michael J. "Differences between mouse and rat pancreatic islets: succinate responsiveness, malic enzyme, and anaplerosis." American Journal of Physiology-Endocrinology and Metabolism 283, no. 2 (2002): E302—E310. http://dx.doi.org/10.1152/ajpendo.00041.2002.

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Succinic acid methyl esters are potent insulin secretagogues in rat pancreatic islets, but they do not stimulate insulin release in mouse islets. Unlike rat and human islets, mouse islets lack malic enzyme and, therefore, are unable to form pyruvate from succinate-derived malate for net synthesis of acetyl-CoA. Dimethyl-[2,3-14C]succinate is metabolized in the citric acid cycle in mouse islets to the same extent as in rat islets, indicating that endogenous acetyl-CoA condenses with oxaloacetate derived from succinate. However, without malic enzyme, the net synthesis from succinate of the citri

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17

Thomas, Daniel J., Marc R. Stammbach, Noel W. Cant, Mark S. Wainwright, and David L. Trimm. "Hydrogenolysis of dimethyl succinate over Raney copper catalyst: a correction." Industrial & Engineering Chemistry Research 29, no. 2 (1990): 204–8. http://dx.doi.org/10.1021/ie00098a009.

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18

TUREK, T., D. L. TRIMM, D. STC BLACK, and N. W. CANT. "ChemInform Abstract: Hydrogenolysis of Dimethyl Succinate on Copper-Based Catalysts." ChemInform 26, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199506041.

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19

Semrad, Susan D. "Comparison of flunixin, prednisolone, dimethyl sulfoxide, and a lazaroid (U74389F) for treating endotoxemic neonatal calves." American Journal of Veterinary Research 54, no. 9 (1993): 1517–22. http://dx.doi.org/10.2460/ajvr.1993.54.09.1517.

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Summary Saline (0.9% NaCl) solution, flunixin meglumine (1.1 mg/kg), prednisolone sodium succinate (1.1 mg/ kg), U74389F (1.5 mg/kg), and dimethyl sulfoxide (0.5 g/kg) were each administered FV to 5 neonatal calves 15 minutes after the start of a 3-hour infusion of Escherichia coli lipopolysaccharide (lps; 2 µg/kg/hr). Four additional calves were given a 3-hour IV infusion of saline solution alone. Only flunixin significantly suppressed eicosanoid production and mitigated clinical signs associated with endotoxemia. Prednisolone provided partial protection against lps-induced hypotension and la

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20

Kristanto, Teofilus, Ping-Sung Tsai, Ardila Hayu Tiwikrama, and Ming-Jer Lee. "Vapor-liquid equilibrium phase behavior of binary systems of carbon dioxide with dimethyl succinate or dimethyl glutarate." Journal of the Taiwan Institute of Chemical Engineers 136 (July 2022): 104402. http://dx.doi.org/10.1016/j.jtice.2022.104402.

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21

Swiderska, Agnieszka, Andrew M. Coney, Abdulaziz A. Alzahrani, et al. "Mitochondrial Succinate Metabolism and Reactive Oxygen Species Are Important but Not Essential for Eliciting Carotid Body and Ventilatory Responses to Hypoxia in the Rat." Antioxidants 10, no. 6 (2021): 840. http://dx.doi.org/10.3390/antiox10060840.

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Reflex increases in breathing in response to acute hypoxia are dependent on activation of the carotid body (CB)—A specialised peripheral chemoreceptor. Central to CB O2-sensing is their unique mitochondria but the link between mitochondrial inhibition and cellular stimulation is unresolved. The objective of this study was to evaluate if ex vivo intact CB nerve activity and in vivo whole body ventilatory responses to hypoxia were modified by alterations in succinate metabolism and mitochondrial ROS (mitoROS) generation in the rat. Application of diethyl succinate (DESucc) caused concentration-d

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22

Chen, Honglin, Lei Zhang, Yulan Huang, Jingjing Lu, Zhijian Zhao, and Xunqiu Wang. "Isobaric vapor–liquid equilibrium of three binary systems containing dimethyl succinate, dimethyl glutarate and dimethyl adipate at 2, 5.2 and 8.3 kPa." Journal of Chemical Thermodynamics 133 (June 2019): 100–110. http://dx.doi.org/10.1016/j.jct.2019.02.006.

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23

Mikolajczak, Kenneth L., Bruce W. Zilkowski, M. Zainul, A. Khan, Cecil R. Smith, and Wendell E. Burkholder. "Attractants for Oryzaephilus surinamensis (L.) (Coleoptera: Cucujidae): dimethyl succinate, glutarate, and adipate." Journal of Agricultural and Food Chemistry 33, no. 6 (1985): 1029–32. http://dx.doi.org/10.1021/jf00066a005.

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24

Rodrigues, Shirley M. M., Vinicius Palaretti, Viviani Nardini, Mauricio G. Constantino, and Gil Valdo J. da Silva. "Studies towards rotational dynamics of dimethyl 2-(triphenylphosphoranylidene) succinate by 1H NMR." Journal of Molecular Structure 1051 (November 2013): 276–79. http://dx.doi.org/10.1016/j.molstruc.2013.08.025.

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25

Kohler, Marc A., Mark S. Wainwright, David L. Trimm, and Noel W. Cant. "Reaction kinetics and selectivity of dimethyl succinate hydrogenolysis over copper-based catalysts." Industrial & Engineering Chemistry Research 26, no. 4 (1987): 652–56. http://dx.doi.org/10.1021/ie00064a003.

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26

İnce, Erol. "Liquid–liquid equilibria of the ternary system water+acetic acid+dimethyl succinate." Fluid Phase Equilibria 238, no. 1 (2005): 33–38. http://dx.doi.org/10.1016/j.fluid.2005.09.013.

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27

Fuse, Hiroyuki, Osamu Takimura, Katsuji Murakami, Yukiho Yamaoka, and Toshio Omori. "Utilization of Dimethyl Sulfide as a Sulfur Source with the Aid of Light by Marinobacterium sp. Strain DMS-S1." Applied and Environmental Microbiology 66, no. 12 (2000): 5527–32. http://dx.doi.org/10.1128/aem.66.12.5527-5532.2000.

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ABSTRACT Strain DMS-S1 isolated from seawater was able to utilize dimethyl sulfide (DMS) as a sulfur source only in the presence of light in a sulfur-lacking medium. Phylogenetic analysis based on 16S ribosomal DNA genes indicated that the strain was closely related toMarinobacterium georgiense. The strain produced dimethyl sulfoxide (DMSO), which was a main metabolite, and small amounts of formate and formaldehyde when grown on DMS as the sole sulfur source. The cells of the strain grown with succinate as a carbon source were able to use methyl mercaptan or methanesulfonate besides DMS but no

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28

Zhi, Chunli, Yang Tang, Jinru Wan, Xingming Liu, Honglin Chen, and Xunqiu Wang. "Determination and correlation of ternary isobaric vapour-liquid equilibrium data of (dimethyl succinate + dimethyl glutarate + dimethyl adipate) at 2, 5 and 8 kPa." Journal of Chemical Thermodynamics 143 (April 2020): 106047. http://dx.doi.org/10.1016/j.jct.2019.106047.

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29

Kacem, Yosra Hadj, Abdelkader Bougarech, Souhir Abid, Majdi Abid, and Etienne Fleury. "Fully Biobased Aliphatic Anionic Oligoesters: Synthesis and Properties." International Journal of Polymer Science 2019 (March 31, 2019): 1–19. http://dx.doi.org/10.1155/2019/3186202.

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Biobased aliphatic sulfonated oligoesters with 10 to 30% of sulfonated units were synthesized by melt polycondensation of biobased monomers such as diethyl succinate, z-octadec-9-enedioic acid, dimer fatty acid, sodium (sulfonated dimethyl succinate), and various diols like 1,4-butane diol and isosorbide. Structural characterization of the resulting oligoesters was determined by 1H NMR spectroscopy and MALDI-TOF MS technique. Showing a regular structure, the nature of the different expected species present in the macromolecular structure allowed the detection of etherification and cyclisation

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30

Liu, Tong, Wei Zou, Wen Zhao, Feng-Bao Zhang, Guo-Liang Zhang, and Qing Xia. "Measurement and correlation for the solubility of dimethyl succinylsuccinate in (methanol+water) and (methanol+dimethyl succinate) binary solvent mixtures." Fluid Phase Equilibria 374 (July 2014): 102–7. http://dx.doi.org/10.1016/j.fluid.2014.04.012.

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31

He, Liangtu, Lei Liu, Yuzhang Huang, et al. "One-pot synthesis of dimethyl succinate from d-fructose using Amberlyst-70 catalyst." Molecular Catalysis 508 (May 2021): 111584. http://dx.doi.org/10.1016/j.mcat.2021.111584.

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32

Api, A. M., D. Belsito, D. Botelho, et al. "RIFM fragrance ingredient safety assessment Dimethyl succinate, CAS Registry Number 106-65-0." Food and Chemical Toxicology 115 (May 2018): S124—S132. http://dx.doi.org/10.1016/j.fct.2017.12.056.

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33

Röschenthaler, G. V., I. Loop, E. Lork, and F. U. Seifert. "Crystal structure of (R,R)-dimethyl 1,2-dihydroxy-1,2-bis(trifluoromethyl) succinate, C8H8F6O6." Zeitschrift für Kristallographie - New Crystal Structures 216, no. 1-4 (2001): 455–56. http://dx.doi.org/10.1524/ncrs.2001.216.14.455.

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34

Sun, Xiuquan, Tsun-mei Chang, Yang Cao, Satomi Niwayama, William L. Hase, and Liem X. Dang. "Solvation of Dimethyl Succinate in a Sodium Hydroxide Aqueous Solution. A Computational Study." Journal of Physical Chemistry B 113, no. 18 (2009): 6473–77. http://dx.doi.org/10.1021/jp901950g.

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35

Puertas, Susana, Francisca Rebolledo, and Vicente Gotor. "Selective ammonolysis and aminolysis of dimethyl succinate. Synthesis of optically active N-alkylsuccinimides." Tetrahedron 51, no. 5 (1995): 1495–502. http://dx.doi.org/10.1016/0040-4020(94)01043-y.

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36

Bhagiyalakshmi, M., J. Herbert Mabel, S. Vishnupriya, M. Palanichamy, and V. Murugesan. "Selective epoxidation of dimethyl maleate to cis-epoxydimethyl succinate over solid acid catalysts." Catalysis Today 141, no. 1-2 (2009): 234–41. http://dx.doi.org/10.1016/j.cattod.2008.07.029.

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37

Thomas, D. J., D. L. Trimm, M. S. Wainwright, and N. W. Cant. "Modelling of the kinetics of the hydrogenolysis of dimethyl succinate over Raney copper." Chemical Engineering and Processing: Process Intensification 31, no. 4 (1992): 241–45. http://dx.doi.org/10.1016/0255-2701(92)87016-a.

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38

Zhumagalieva, Sh N., M. K. Beisebekov, and Zh A. Abilov. "Immobilization of 2,5-dimethyl-4-benzoyl-oxypiperidine succinate over polyacrylic acid (PAA) gels. II. Study of quantitative characteristics of immobilization of succinate of 2,5-dimethyl-4-benzoyl-oxypiperidine over PAA." Journal of Applied Polymer Science 96, no. 4 (2005): 1187–92. http://dx.doi.org/10.1002/app.21329.

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39

Zhumagalieva, Sh N., M. K. Beisebekov, and Zh A. Abilov. "Immobilization of 2,5-dimethyl-4-benzoyl-oxypiperidine succinate over polyacrylic acid (PAA) gels. I. Study of interaction between linear and network PAA with succinate of 2,5-dimethyl-4-benzoyl-oxypiperidine." Journal of Applied Polymer Science 96, no. 4 (2005): 1183–86. http://dx.doi.org/10.1002/app.21330.

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40

Bejaei, Cliff, Madilao, and vanVuuren. "Modelling Changes in Volatile Compounds in British Columbian Varietal Wines that Were Bottle Aged for Up to 120 Months." Beverages 5, no. 3 (2019): 57. http://dx.doi.org/10.3390/beverages5030057.

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This research quantified 46 volatile compounds in vintage wines (1998–2005) from British Columbia (BC), which had been bottle-aged for up to 120 months. Wines were analyzed up to five times, between December 2003 and October 2008. Compounds were identified using gas chromatography mass spectrometry (GC-MS) and their concentrations were related to “wine age” using single linear regression (SLR). SLR models were developed for each wine compound (eight alcohol, 12 ester/acetate, one acid, one aldehyde, one sulfur) in eight varietal wines: six red (Cabernet franc, Cabernet Sauvignon, Meritage, Mer

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41

Olson, M. J., J. L. Martin, A. C. LaRosa, A. N. Brady, and L. R. Pohl. "Immunohistochemical localization of carboxylesterase in the nasal mucosa of rats." Journal of Histochemistry & Cytochemistry 41, no. 2 (1993): 307–11. http://dx.doi.org/10.1177/41.2.8419465.

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The enzymatic esterase activity of carboxylesterases is integral to the nasal toxicity of many esters used as industrial solvents or in polymer manufacture, including propylene glycol monomethyl ether acetate, dimethyl glutarate, dimethyl succinate, dimethyl adipate, and ethyl acrylate. Inhalation of these chemicals specifically damages the olfactory mucosa of rodents. We report the localization and differential distribution of a 59 KD carboxylesterase in nasal tissues of the rat by immunohistochemistry. Rabbit antiserum against the 59 KD rat liver microsomal carboxylesterase bound most promin

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42

Yang, Xingchuan, Genlei Wei, Xiangmeng Chen, Li Xu, and Guoji Liu. "Liquid–Liquid Equilibrium Measurement and Correlation for the Ternary Systems (Dimethyl Succinate + 1,4-Butanediol)/(Dimethyl Glutarate + 1,5-Pentanediol)/(Dimethyl Adipate + 1,6-Hexanediol) + Water at Different Temperatures." Journal of Chemical & Engineering Data 65, no. 4 (2020): 1875–85. http://dx.doi.org/10.1021/acs.jced.9b01099.

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43

Cobo, J., S. Molina, A. Sánchez, M. Nogueras та J. N. Low. "Dimethyl 2-(6-benzyloxy-2-methylthiopyrimidin-4-yl)imino-3-(triphenyl-λ5-phosphanylidene)succinate". Acta Crystallographica Section C Crystal Structure Communications 55, № 12 (1999): IUC9900150. http://dx.doi.org/10.1107/s0108270199098315.

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44

Wan, Xinyan, Dezhang Ren, Yunjie Liu, et al. "Facile Synthesis of Dimethyl Succinate via Esterification of Succinic Anhydride over ZnO in Methanol." ACS Sustainable Chemistry & Engineering 6, no. 3 (2018): 2969–75. http://dx.doi.org/10.1021/acssuschemeng.7b02598.

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45

López-Garzón, Camilo S., Luuk A. M. van der Wielen, and Adrie J. J. Straathof. "Green upgrading of succinate using dimethyl carbonate for a better integration with fermentative production." Chemical Engineering Journal 235 (January 2014): 52–60. http://dx.doi.org/10.1016/j.cej.2013.09.017.

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46

Brett, Gemma L., Peter J. Miedziak, David W. Knight, Stuart H. Taylor, and Graham J. Hutchings. "Gold-Based Nanoparticulate Catalysts for the Oxidative Esterification of 1,4-Butanediol to Dimethyl Succinate." Topics in Catalysis 57, no. 6-9 (2013): 723–29. http://dx.doi.org/10.1007/s11244-013-0229-5.

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47

Shekhawat, Dushyant, James E. Jackson, and Dennis J. Miller. "Process model and economic analysis of itaconic acid production from dimethyl succinate and formaldehyde." Bioresource Technology 97, no. 2 (2006): 342–47. http://dx.doi.org/10.1016/j.biortech.2005.02.036.

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48

Kasinathan, Palraj, Dong Won Hwang, U.-Hwang Lee, Young Kyu Hwang, and Jong-San Chang. "Effect of Cu particle size on hydrogenation of dimethyl succinate over Cu–SiO2 nanocomposite." Catalysis Communications 41 (November 2013): 17–20. http://dx.doi.org/10.1016/j.catcom.2013.06.034.

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49

Brett, Gemma L., Peter J. Miedziak, Qian He, et al. "Gold-Nanoparticle-Based Catalysts for the Oxidative Esterification of 1,4-Butanediol into Dimethyl Succinate." ChemSusChem 6, no. 10 (2013): 1952–58. http://dx.doi.org/10.1002/cssc.201300420.

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50

Andriychenko, E. O., V. I. Zelenov, A. V. Bespalov, et al. "Copper(II) succinate: electrochemical synthesis, characterization and application as a precursor for micron-sized copper(II) oxide fibers." Žurnal obŝej himii 94, no. 5 (2024): 639–48. http://dx.doi.org/10.31857/s0044460x24050119.

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Abstract:

A coordination compound of copper(II) with succinic acid was obtained by electrochemical synthesis in media of various compositions. The samples were characterized by methods of quantitative analysis, ESR and IR spectroscopy, synchronous thermal analysis. The vibrational frequencies of copper(II) succinate were calculated by using DFT and the experimental IR spectra were interpreted on the basis of the results. Micro-sized copper(II) oxide fibers were obtained by thermal decomposition of synthesized samples. It was shown that the use of the water–dimethyl sulfoxide system with a volume ratio 1

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