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Journal articles on the topic 'Furoic acid'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

He, Wei, Yucai He, and Jianren Ye. "Efficient Synthesis of Biobased Furoic Acid from Corncob via Chemoenzymatic Approach." Processes 10, no. 4 (2022): 677. http://dx.doi.org/10.3390/pr10040677.

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Valorization of lignocellulosic materials into value-added biobased chemicals is attracting increasing attention in the sustainable chemical industry. As an important building block, furoic acid has been commonly utilized to manufacture polymers, flavors, perfumes, bactericides, fungicides, etc. It is generally produced through the selective oxidation of furfural. In this study, we provide the results of the conversion of biomass-based xylose to furoic acid in a chemoenzymatic cascade reaction with the use of a heterogeneous chemocatalyst and a dehydrogenase biocatalyst. For this purpose, NaOH

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2

Kriechbaum, Ricarda, Oliver Spadiut, and Julian Kopp. "Bioconversion of Furanic Compounds by Chlorella vulgaris—Unveiling Biotechnological Potentials." Microorganisms 12, no. 6 (2024): 1222. http://dx.doi.org/10.3390/microorganisms12061222.

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Lignocellulosic biomass is abundant on Earth, and there are multiple acidic pretreatment options to separate the cellulose, hemicellulose, and lignin fraction. By doing so, the fermentation inhibitors 5-Hydroxymethylfurfural (HMF) and furfural (FF) are produced in varying concentrations depending on the hydrolyzed substrate. In this study, the impact of these furanic compounds on Chlorella vulgaris growth and photosynthetic activity was analyzed. Both compounds led to a prolonged lag phase in Chlorella vulgaris growth. While the photosynthetic yield Y(II) was not significantly influenced in cu

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3

Parkin, Andrew, Martin Adam, Suzanne M. Harte, Jennifer L. Kennedy, and Chick C. Wilson. "4-Ethoxycarbonyl-3-furoic acid." Acta Crystallographica Section E Structure Reports Online 62, no. 3 (2006): o987—o989. http://dx.doi.org/10.1107/s1600536806004429.

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4

Lu, Zhixiang, Bo Lang, Shaoqing Wang, Hongyi Liu, Xinhua Wang, and Jie Chen. "Elucidating the Fundamental Process of Methyl-(5hydroxymethyl) Furan-2-Carboxylate Toxin Biosynthesis in Curvularia lunata Causing Maize Leaf Spot." Journal of Fungi 10, no. 10 (2024): 688. http://dx.doi.org/10.3390/jof10100688.

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Maize leaf spot, which is caused by Curvularia lunata (Wakkre) Boedijn, was epidemic in the maize-growing regions of northeastern and northern China in the mid-1990s, where it led to large yield losses. Since then, the epidemic has evolved into a kind of common disease. In recent years, however, a tendency of becoming an epidemic disease again has been observed in some areas in China due to significant changes in climate, farming, systems and crop varieties. The significance of methyl-(5hydroxymethyl) furan-2-carboxylate (M5HF2C) as a nonspecific host toxin in causing maize leaf spot disease h

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5

Nguyen, Hannah, Yunzhu Wang, David Moglia, et al. "Production of renewable oleo-furan surfactants by cross-ketonization of biomass-derived furoic acid and fatty acids." Catalysis Science & Technology 11, no. 8 (2021): 2762–69. http://dx.doi.org/10.1039/d0cy02349c.

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6

Choi, Sun-Il, Xionggao Han, Xiao Men, et al. "Benincasa hispida Extract Prevents Ovariectomy-Induced Osteoporosis in Female ICR Mice." Applied Sciences 13, no. 2 (2023): 832. http://dx.doi.org/10.3390/app13020832.

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With the increase in bone metabolic diseases owing to the aging of the global population, interest in functional food ingredients for improving bone health is increasing. This study aimed to determine the anti-osteoporosis effect of Benincasa hispida extract (BHE, HR1901-W) and 2-furoic acid in ovariectomy (OVX)-induced osteoporosis in female ICR mice. Thirty-five female ICR mice underwent OVX or sham operation and were randomized into seven groups of five animals as follows: normal, sham, OVX, OVX with genistein (10 mg/kg), 2-furoic acid (20 mg/kg), LBHE (100 mg/kg), and HBHE (200 mg/kg). Aft

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7

Holewinski, Adam. "Electro-Oxidative Valorization of Biomass-Derived Furanics." ECS Meeting Abstracts MA2023-02, no. 27 (2023): 1428. http://dx.doi.org/10.1149/ma2023-02271428mtgabs.

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Electrocatalysis poses many potential advantages for distributed scale biomass valorization. Furanic biomass derivatives such as furfural and 5-hydroxymethylfurfural (HMF) can provide access to a number of value-added chemicals by partial oxidation, including furoic acid, maleic acid, and 2,5-furandicarboxylic acid (FDCA). Here, we have utilized differential reactor studies with online electrochemical mass spectrometry (OLEMS), as well as in-situ attenuated total reflectance surface enhanced infrared reflection absorption spectroscopy (ATR-SEIRAS), to probe these reaction pathways on various m

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8

Dick, Graham R., Amy D. Frankhouser, Aanindeeta Banerjee, and Matthew W. Kanan. "A scalable carboxylation route to furan-2,5-dicarboxylic acid." Green Chemistry 19, no. 13 (2017): 2966–72. http://dx.doi.org/10.1039/c7gc01059a.

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9

DEADY, L., and R. SHANKS. "A Convenient Preparation of 3-Furoic Acid." Synthesis 1972, no. 10 (2002): 571. http://dx.doi.org/10.1055/s-1972-21937.

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10

Cioc, Răzvan C., Tom J. Smak, Marc Crockatt, Jan C. van der Waal, and Pieter C. A. Bruijnincx. "Furoic acid and derivatives as atypical dienes in Diels–Alder reactions." Green Chemistry 23, no. 15 (2021): 5503–10. http://dx.doi.org/10.1039/d1gc01535d.

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11

Dixit, Ram Ji, Aditya Singh, Vijay K. Ramani, and Suddhasatwa Basu. "Electrocatalytic hydrogenation of furfural paired with photoelectrochemical oxidation of water and furfural in batch and flow cells." Reaction Chemistry & Engineering 6, no. 12 (2021): 2342–53. http://dx.doi.org/10.1039/d1re00080b.

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12

Du, Genlai, Xia Hua, Bin Xu, Huan Wang, Xin Zhou, and Yong Xu. "The processing-module assembly strategy for continuous bio-oxidation of furan chemicals by integrated and coupled biotechnology." Green Chemistry 23, no. 3 (2021): 1330–36. http://dx.doi.org/10.1039/d0gc03300f.

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13

Xie, Fan, Sethupathy Mahendiran, Nathan A. Seifert, and Yunjie Xu. "Modifying conformational distribution of chiral tetrahydro-2-furoic acid through its interaction with water: a rotational spectroscopic and theoretical investigation." Physical Chemistry Chemical Physics 23, no. 6 (2021): 3820–25. http://dx.doi.org/10.1039/d0cp06265k.

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14

Salis, Severyn, Nadia Spano, Marco Ciulu, Ignazio Floris, Maria I. Pilo, and Gavino Sanna. "Electrochemical Determination of the “Furanic Index” in Honey." Molecules 26, no. 14 (2021): 4115. http://dx.doi.org/10.3390/molecules26144115.

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5-(hydroxymethyl)furan-2-carbaldehyde, better known as hydroxymethylfurfural (HMF), is a well-known freshness parameter of honey: although mostly absent in fresh samples, its concentration tends to increase naturally with aging. However, high quantities of HMF are also found in fresh but adulterated samples or honey subjected to thermal or photochemical stresses. In addition, HMF deserves further consideration due to its potential toxic effects on human health. The processes at the origin of HMF formation in honey and in other foods, containing saccharides and proteins—mainly non-enzymatic bro

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15

Douthwaite, Mark, Xiaoyang Huang, Sarwat Iqbal, et al. "The controlled catalytic oxidation of furfural to furoic acid using AuPd/Mg(OH)2." Catalysis Science & Technology 7, no. 22 (2017): 5284–93. http://dx.doi.org/10.1039/c7cy01025g.

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16

Chacón-Huete, F., C. Messina, F. Chen, L. Cuccia, X. Ottenwaelder, and P. Forgione. "Solvent-free mechanochemical oxidation and reduction of biomass-derived 5-hydroxymethyl furfural." Green Chemistry 20, no. 23 (2018): 5261–65. http://dx.doi.org/10.1039/c8gc02481b.

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17

Roselli, Alessandra, Yuri Carvalho, Franck Dumeignil, Fabrizio Cavani, Sébastien Paul, and Robert Wojcieszak. "Liquid Phase Furfural Oxidation under Uncontrolled pH in Batch and Flow Conditions: The Role of In Situ Formed Base." Catalysts 10, no. 1 (2020): 73. http://dx.doi.org/10.3390/catal10010073.

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Selective oxidation of furfural to furoic acid was performed with pure oxygen in aqueous phase under mild conditions and uncontrolled pH using hydrotalcite-supported gold nanoparticles as catalyst. Hydrotalcites with different Mg: Al ratios were tested as support. The effects of reaction time, temperature and furfural/catalyst ratio were evaluated. The catalyst Au/HT 4:1 showed the highest activity and selectivity to the desired product, achieving a complete conversion of furfural to furoic acid after 2 h at 110 °C. Further, stability tests were carried out in a continuous stirred-tank reactor

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18

Payne, Karl A. P., Stephen A. Marshall, Karl Fisher, et al. "Enzymatic Carboxylation of 2-Furoic Acid Yields 2,5-Furandicarboxylic Acid (FDCA)." ACS Catalysis 9, no. 4 (2019): 2854–65. http://dx.doi.org/10.1021/acscatal.8b04862.

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19

RAJESH, NAGAR, and C. SHARMA R. "Structural and Biocidal Studies of Ternary Complexes of some Transition Metals." Journal of Indian Chemical Society Vol. 66, May 1989 (1989): 337–38. https://doi.org/10.5281/zenodo.6163874.

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Department of Chemistry, Institute of Basic Sciences, Agra University.,Agra-282 002 <em>Manuscript received 11 November 1987, revised 26 October 1988, accepted 28 February 1989</em> Structural and Biocidal Studies of Ternary Complexes of some Transition Metals 

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20

Ketkaew, Marisa, Sunpet Assavapanumat, Sorasak Klinyod, Alexander Kuhn, and Chularat Wattanakit. "Bifunctional Pt/Au Janus electrocatalysts for simultaneous oxidation/reduction of furfural with bipolar electrochemistry." Chemical Communications 58, no. 27 (2022): 4312–15. http://dx.doi.org/10.1039/d1cc06759a.

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We report the simultaneous electro-oxidation/-reduction of biomass-derived furfural in a one-pot approach, using bipolar electrochemistry with bifunctional Pt/Au Janus electrocatalysts, selectively into both, furfuryl alcohol and furoic acid.

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21

Sárvári Horváth, Ilona, Carl Johan Franzén, Mohammad J. Taherzadeh, Claes Niklasson, and Gunnar Lidén. "Effects of Furfural on the Respiratory Metabolism of Saccharomyces cerevisiae in Glucose-Limited Chemostats." Applied and Environmental Microbiology 69, no. 7 (2003): 4076–86. http://dx.doi.org/10.1128/aem.69.7.4076-4086.2003.

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ABSTRACT Effects of furfural on the aerobic metabolism of the yeast Saccharomyces cerevisiae were studied by performing chemostat experiments, and the kinetics of furfural conversion was analyzed by performing dynamic experiments. Furfural, an important inhibitor present in lignocellulosic hydrolysates, was shown to have an inhibitory effect on yeast cells growing respiratively which was much greater than the inhibitory effect previously observed for anaerobically growing yeast cells. The residual furfural concentration in the bioreactor was close to zero at all steady states obtained, and it

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22

Bistocchi, Giovanni Allunni, Giovanni De Meo, Mauro Pedini, Adolfo Ricci, and Pierre Jacquignon. "Alkylating activity of polyphosphate ester in the course of the synthesis of benzimidazoles." Collection of Czechoslovak Chemical Communications 50, no. 9 (1985): 1959–61. http://dx.doi.org/10.1135/cccc19851959.

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5-Fluoro-2-(5-nitrofuryl)benzimidazole (I) was synthesized from 4-fluoro-1,2-diaminobenzene and 5-nitro-2-furoic acid using ethyl polyphosphate as cyclization reagent. N-Ethyl derivative was isolated as by-product in substantial amount.

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23

Klein, Larry L. "Convenient Synthesis of 2, 5-Dimethyl-2-Furoic Acid." Synthetic Communications 16, no. 4 (1986): 431–35. http://dx.doi.org/10.1080/00397918608057719.

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24

Petrosyan, A. M., V. V. Ghazaryan, and M. Fleck. "On the existence of “l-alanine 2-furoic acid”." Optik 125, no. 21 (2014): 6609–10. http://dx.doi.org/10.1016/j.ijleo.2014.08.027.

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25

Hall, Iris H., Oi T. Wong, David J. Reynolds, and J. J. Chang. "Hypolipidemic Effects of 2-Furoic Acid inSprague-Dawley Rats." Archiv der Pharmazie 326, no. 1 (1993): 15–23. http://dx.doi.org/10.1002/ardp.19933260105.

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26

Tran‐Cong, Nam Michael, Attila Mándi, Sándor Balázs Király, et al. "Furoic acid derivatives from the endophytic fungus Coniothyrium sp." Chirality 32, no. 5 (2020): 605–10. http://dx.doi.org/10.1002/chir.23209.

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27

Otto, David A., Chris Chatzidakis, Eva Kasziba, and George A. Cook. "Reciprocal effects of 5-(tetradecyloxy)-2-furoic acid on fatty acid oxidation." Archives of Biochemistry and Biophysics 242, no. 1 (1985): 23–31. http://dx.doi.org/10.1016/0003-9861(85)90475-8.

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28

Nichols, Nancy N., Tristan A. Lunde, Kevin C. Graden, et al. "Chemotaxis to Furan Compounds by Furan-Degrading Pseudomonas Strains." Applied and Environmental Microbiology 78, no. 17 (2012): 6365–68. http://dx.doi.org/10.1128/aem.01104-12.

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ABSTRACTTwoPseudomonasstrains known to utilize furan derivatives were shown to respond chemotactically to furfural, 5-hydroxymethylfurfural, furfuryl alcohol, and 2-furoic acid. In addition, a LysR-family regulatory protein known to regulate furan metabolic genes was found to be involved in regulating the chemotactic response.

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29

K., S. GUPTA, KUMAR DINESH, BHARGAVA RACHNA, RANI ASHU, and S. N. PRASAD D. "Kinetics and Mechanism of Thallium(III)- Ligand Electron Transfer Reactions. Oxidation of 2-Furoic Acid in Perchloric Acid Solutions." Journal Of Indian Chemical Society Vol.66, Aug-Oct 1989 (1989): 619–27. https://doi.org/10.5281/zenodo.6010225.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004 In the oxidation of 2-furoic acid (HFA) with thallic perchlorate at 55˚, several TI<sup>III</sup>-HFA complexes are formed and the complex TI(HFA)\(^{2+}_3\)appears to be only reactive species. When at constant [TI<sup>III</sup>]<sub>1</sub> the HF A Is increased the rate profile passes through a maximum. At very high [HFA]T/[TI<sup>III</sup>]<sub>T</sub> ratio, the following rate law is obeyed,                                       &nb

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30

Lutsenko, Irina A., Dmitry E. Baravikov, Kseniya A. Koshenskova, et al. "What are the prospects for using complexes of copper(ii) and zinc(ii) to suppress the vital activity of Mycolicibacterium smegmatis?" RSC Advances 12, no. 9 (2022): 5173–83. http://dx.doi.org/10.1039/d1ra08555g.

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New complexes of zinc(ii) and copper(ii) with 2-furoic acid (Hfur), acetic acids and N-donor ligands with the compositions [Zn2(fur)4]n, [Zn2(fur)4(NH2py)2], [Zn(fur)2(neoc)], [Zn(OAc)2(neoc)], and [Cu(fur)2(neoc)(H2O)] were synthesized.

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31

Schwarz, Mónica, Fabian Weber, Enrique Durán-Guerrero, et al. "HPLC-DAD-MS and Antioxidant Profile of Fractions from Amontillado Sherry Wine Obtained Using High-Speed Counter-Current Chromatography." Foods 10, no. 1 (2021): 131. http://dx.doi.org/10.3390/foods10010131.

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In the present work, the polyphenolic profile of a complex matrix such as Amontillado sherry has been processed by means of high-speed counter-current chromatography (HSCCC) and characterized by HPLC-DAD-MS. An Amberlite XAD-7 column was used to obtain the wine extract, and three different biphasic solvent systems were applied for HSCCC separation: MTBE (methyl tert-butyl ether)/n-butanol/acetonitrile/water (1.1/3/1.1/5+0.1% trifluoroacetic acid), MTBE/n-butanol/acetonitrile/water (2/2/1/5), and hexane/ethyl acetate/ethanol/water (1/5/1/5). As a result, 42 phenolic compounds and furanic deriva

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32

Schwarz, Mónica, Fabian Weber, Enrique Durán-Guerrero, et al. "HPLC-DAD-MS and Antioxidant Profile of Fractions from Amontillado Sherry Wine Obtained Using High-Speed Counter-Current Chromatography." Foods 10, no. 1 (2021): 131. http://dx.doi.org/10.3390/foods10010131.

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In the present work, the polyphenolic profile of a complex matrix such as Amontillado sherry has been processed by means of high-speed counter-current chromatography (HSCCC) and characterized by HPLC-DAD-MS. An Amberlite XAD-7 column was used to obtain the wine extract, and three different biphasic solvent systems were applied for HSCCC separation: MTBE (methyl tert-butyl ether)/n-butanol/acetonitrile/water (1.1/3/1.1/5+0.1% trifluoroacetic acid), MTBE/n-butanol/acetonitrile/water (2/2/1/5), and hexane/ethyl acetate/ethanol/water (1/5/1/5). As a result, 42 phenolic compounds and furanic deriva

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33

Wu, Xu, Heqin Guo, Litao Jia, Yong Xiao, Bo Hou, and Debao Li. "Effect of MnO2 Crystal Type on the Oxidation of Furfural to Furoic Acid." Catalysts 13, no. 4 (2023): 663. http://dx.doi.org/10.3390/catal13040663.

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The base-free oxidation of furfural by non-noble metal systems has been challenging. Although MnO2 emerges as a potential catalyst application in base-free conditions, its catalytic efficiency still needs to be improved. The crystalline form of MnO2 is an important factor affecting the oxidation ability of furfural. For this reason, four crystalline forms of MnO2 (α, β, γ, and δ-MnO2) were selected. Their oxidation performance and surface functional groups were analyzed and compared in detail. Only δ-MnO2 exhibited excellent activity, achieving 99.04% furfural conversion and 100% Propo.FA (Onl

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34

Pevzner, L. M. "Synthesis and selected reactions of 4-(diethoxyphosphorylmethyl)-3-furoic acid." Russian Journal of General Chemistry 82, no. 3 (2012): 404–12. http://dx.doi.org/10.1134/s1070363212030073.

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35

Liu, Shengqin, and Jason Chun-Ho Lam. "One-Pot Electrosynthesis of Gamma-Butyrolactone (GBL) from Furoic Acid." ECS Meeting Abstracts MA2024-01, no. 56 (2024): 2974. http://dx.doi.org/10.1149/ma2024-01562974mtgabs.

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The catalytic valorization of biomass to afford synthetically useful small molecules is essential for sustainable biorefinery processes. Herein, we present a mild cascaded electrochemical protocol for converting furoic acid (FA), a common biomass-derived feedstock, into a versatile platform chemical, gamma-butyrolactone (GBL). All involved species participate in the desired redox pathway with high selectivity: FA was electrochemically oxidized with 84.2% selectivity to 2(5H)-furanone (2-FO), the olefin of which was then hydrogenated to yield GBL with 98.5% selectivity. We identified that a cer

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36

Donohoe, Timothy J., Madeleine Helliwell, Clare A. Stevenson, and Tamara Ladduwahetty. "Stereoselectivity in the Birch reduction of 2-furoic acid derivatives." Tetrahedron Letters 39, no. 19 (1998): 3071–74. http://dx.doi.org/10.1016/s0040-4039(98)00361-x.

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37

Navio, J. A., J. Fuentes Mota, M. A. Pradera Adrian, and M. Garcia Gomez. "Oxidation of 2-furoic acid via singlet oxygen generated photochemically." Journal of Photochemistry and Photobiology A: Chemistry 52, no. 1 (1990): 91–95. http://dx.doi.org/10.1016/1010-6030(90)87094-r.

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38

Gilman, Henry, Robert R. Burtner, and E. Westley Smith. "Orientation in the furan nucleus. 2-methyl-3-furoic acid." Recueil des Travaux Chimiques des Pays-Bas 51, no. 5 (2010): 407–10. http://dx.doi.org/10.1002/recl.19320510503.

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39

Liu, Tian-Tian, Xiao-Rong He, Run-Xue Xu, et al. "Inhibitory mechanism and molecular analysis of furoic acid and oxalic acid on lipase." International Journal of Biological Macromolecules 120 (December 2018): 1925–34. http://dx.doi.org/10.1016/j.ijbiomac.2018.09.150.

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40

Martin, Alex. "Synthesis, Characterization and Screening of Anti-tubercular activity of 2, 5-Disubstituted-1, 3, 4-Oxadiazole." Indian Journal of Pharmaceutical and Biological Research 1, no. 03 (2013): 12–19. http://dx.doi.org/10.30750/ijpbr.1.3.3.

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The synthesis of 2-furyl-5-(substituted)-1,3,4-oxadiazoles was carried out by microwave irradiation of 2-furoic acid and ethanol followed by subsequent hydrazinolysis with hydrazine hydrate. Finally furan-2-acid hydrazide was treated with appropriate carboxylic acid in the presence of phosphorous oxychloride to produce title compounds. The structures of the newly synthesized compounds were established on the basis of spectral analysis such as IR, H1NMR and Mass spectral data. The synthesized compounds were screened for their anti-tubercular activity.

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41

Kimura, Yasuo, Satoko Tani, Asami Hayashi, et al. "Nematicidal Activity of 5-Hydroxymethyl-2-furoic Acid against Plant-Parasitic Nematodes." Zeitschrift für Naturforschung C 62, no. 3-4 (2007): 234–38. http://dx.doi.org/10.1515/znc-2007-3-413.

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Abstract A nematicide, 5-hydroxymethyl-2-furoic acid (1), was isolated from cultures of the fungus Aspergillus sp. and its structure was identified by spectroscopic analysis. Compound 1 showed effective nematicidal activities against the pine wood nematode Bursaphelenchus xylophilus and the free-living nematode Caenorhabditis elegans without inhibitory activity against plant growth, but 1 did not show any effective nematicidal activity against Pratylenchus penetrans.

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42

Babu, A. Ravindra, J. S. V. M. Lingeswara Rao, D. Murali Krishna, and R. Sambasiva Rao. "Acid—base equilibria of 2-furoic acid hydrazide and adipic acid dihydrazide in aqueous—organic media." Analytica Chimica Acta 306, no. 2-3 (1995): 297–300. http://dx.doi.org/10.1016/0003-2670(94)00688-i.

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43

Nichols, Nancy N., and Jeffrey A. Mertens. "Identification and transcriptional profiling ofPseudomonas putidagenes involved in furoic acid metabolism." FEMS Microbiology Letters 284, no. 1 (2008): 52–57. http://dx.doi.org/10.1111/j.1574-6968.2008.01196.x.

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44

Yang, Dong, Cuiluan Ma, Bo Peng, Jianhe Xu, and Yu-Cai He. "Synthesis of furoic acid from biomass via tandem pretreatment and biocatalysis." Industrial Crops and Products 153 (October 2020): 112580. http://dx.doi.org/10.1016/j.indcrop.2020.112580.

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45

Chai, Wei-Ming, Xuan Liu, Yong-Hua Hu, et al. "Antityrosinase and antimicrobial activities of furfuryl alcohol, furfural and furoic acid." International Journal of Biological Macromolecules 57 (June 2013): 151–55. http://dx.doi.org/10.1016/j.ijbiomac.2013.02.019.

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46

Gilman, Henry, and M. B. Lousinian. "An improved procedure for the preparation of furan from furoic acid." Recueil des Travaux Chimiques des Pays-Bas 52, no. 2 (2010): 156–59. http://dx.doi.org/10.1002/recl.19330520209.

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47

Brzić, Saša, Nataša Knežević, Tihomir Kovačević, Marija Vuksanović, Aleksandar Marinković, and Jelena Gržetić. "Furoic acid-based (non)energetic plasticizers for solid composite propellants production." Scientific Technical Review 74, no. 1 (2024): 50–55. https://doi.org/10.5937/str2401050b.

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This paper presents the development of high-performance energetic plasticizers based on furan-2,5-dicarboxylic acid (FDCA) as a renewable bio-material, resulting in bis(2-ethylhexyl) furan-2,5-dicarboxylate (FDC) and bis(1,3-diazidopropan-2-yl) furan-2,5-dicarboxylate (FDAC). The structural characterization was performed using FTIR spectroscopy. The effects of FDCA-based plasticizers were analyzed in the binder component of composite rocket propellants (CRP) as well as in ammonium perchlorate-based CRP, and the results were compared with those obtained for the commercial plasticizer dioctyl ad

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48

Kim, Jiwon, Hyeoncheol Francis Son, Sungmin Hwang, et al. "Improving Lipid Production of Yarrowia lipolytica by the Aldehyde Dehydrogenase-Mediated Furfural Detoxification." International Journal of Molecular Sciences 23, no. 9 (2022): 4761. http://dx.doi.org/10.3390/ijms23094761.

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Abstract:

Yarrowia lipolytica, the non-conventional yeast capable of high lipogenesis, is a microbial chassis for producing lipid-based biofuels and chemicals from renewable resources such as lignocellulosic biomass. However, the low tolerance of Y. lipolytica against furfural, a major inhibitory furan aldehyde derived from the pretreatment processes of lignocellulosic biomass, has restricted the efficient conversion of lignocellulosic hydrolysates. In this study, the furfural tolerance of Y. lipolytica has been improved by supporting its endogenous detoxification mechanism. Specifically, the endogenous

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49

Kim, Jiwon, Hyeoncheol Francis Son, Sungmin Hwang, et al. "Improving Lipid Production of Yarrowia lipolytica by the Aldehyde Dehydrogenase-Mediated Furfural Detoxification." International Journal of Molecular Sciences 23, no. 9 (2022): 4761. http://dx.doi.org/10.3390/ijms23094761.

Full text

Abstract:

Yarrowia lipolytica, the non-conventional yeast capable of high lipogenesis, is a microbial chassis for producing lipid-based biofuels and chemicals from renewable resources such as lignocellulosic biomass. However, the low tolerance of Y. lipolytica against furfural, a major inhibitory furan aldehyde derived from the pretreatment processes of lignocellulosic biomass, has restricted the efficient conversion of lignocellulosic hydrolysates. In this study, the furfural tolerance of Y. lipolytica has been improved by supporting its endogenous detoxification mechanism. Specifically, the endogenous

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50

Hong, Min, Han-Dong Yin та Da-Qi Wang. "Bis[μ-furan-2-carbaldehyde (1-carboxyethylidene)hydrazonato(2–)]bis[methanoldimethyltin(IV)]". Acta Crystallographica Section E Structure Reports Online 62, № 7 (2006): m1555—m1557. http://dx.doi.org/10.1107/s1600536806017612.

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Abstract:

In the title complex, [Sn2(CH3)4(C8H6N2O4)2(CH4O)2], each SnIV ion exists in a distorted pentagonal–bipyramidal coordination environment, coordinated by three O atoms and one N atom from the pyruvic acid 2-furoic acid hydrazone ligands, one O atom from a methanol molecule and two axial C atoms from trans methyl groups, thus forming a dimeric molecule, which has crystallographic \overline{1} symmetry. In the dimeric structure there are also intramolecular hydrogen bonds, which contribute to the crystal stability and compactness.

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