Relevant bibliographies by topics / Furan derivatives

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Furan derivatives'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Furan derivatives"

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Duc, Dau Xuan. "Recent Achievement in the Synthesis of Benzo[b]furans." Current Organic Synthesis 17, no. 7 (2020): 498–517. http://dx.doi.org/10.2174/1570179417666200625212639.

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Background: Benzo[b]furan derivatives are oxygen-containing heterocyclic compounds consisting of fused benzene and furan rings and are present in a large number of natural and non-natural compounds. This class of compounds has a wide spectrum of biological activities, such as antiarrhythmic, anticancer, inflammatory, antioxidant, antimicrobial, and antiviral. Furthermore, benzo[b]furan derivatives have also been applied in various areas, such as organic electroluminescence device materials and organic dyes, photosensitizing material, organic synthesis as building blocks or intermediates. : Bec
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Hana, Saeid1* Hadeel Al-sayed2 Marwa Bader2. "A Review on Biological and Medicinal Significance of Furan." Alq J Med App Sci 6, no. 1 (2023): 44–58. https://doi.org/10.5281/zenodo.7650255.

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An important group of heterocyclic compounds with significant biological characteristics are furan derivatives. The creation of furan derivatives and their testing for various pharmacological properties have received a lot of attention over the past few decades. Various substances with anti-bacterial properties have a fundamental skeleton made up of furan rings. These molecules are frequently used in antiviral, antifungal, anti-inflammatory, analgesic, antidepressant, anti-anxiolytic, anti-parkinsonian, anti-glaucoma, muscle relaxant, antihypertensive, diuretic, anti-ulcer, anti-ageing, and an
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Albrand, Michel, René Dolmazon, and Patrick Pollet. "Synthèse, structure et études spectroscopiques RMN 1H et 13C de dérivés perhydrocyclododéca[b]furaniques." Canadian Journal of Chemistry 69, no. 3 (1991): 521–27. http://dx.doi.org/10.1139/v91-078.

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A synthetic route to perhydrocyclododeca[b]furan-3-ols, perhydrocyclododeca[b]furan-3-ones, and perhydrocyclododeca[b]furan derivatives is described. Their configurations were determined. For the perhydrocyclododeca[b]furan-3-one and perhydrocyclododeca[b]furan pairs, the cis isomer was much less stable than the trans isomer. This agrees well with results from a conformational analysis, carried out by molecular mechanics. The 1H and l3C NMR spectra are reported. Key words: perhydrocyclododeca[b]furans, conformations, force field calculations, 1H and 13C NMR.
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Yadav, Maruti B., and Yeon Tae Jeong. "A one-pot ring-closure and ring-opening sequence for the cascade synthesis of dihydrofurofurans and functionalized furans." Organic & Biomolecular Chemistry 19, no. 34 (2021): 7409–19. http://dx.doi.org/10.1039/d1ob01300a.

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Hasimujiang, Balati, Shengsheng Lin, Chengwei Zheng, Yong Zeng, and Zhixiong Ruan. "Direct Electrooxidative Selenylation/Cyclization of Alkynes: Access to Functionalized Benzo[b]furans." Molecules 27, no. 19 (2022): 6314. http://dx.doi.org/10.3390/molecules27196314.

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A mild, practical, metal and oxidant-free methodology for the synthesis of various C-3 selenylated benzo[b]furan derivatives was developed through the intramolecular cyclization of alkynes promoted with diselenides via electrooxidation. A wide range of selenium-substituted benzo[b]furan derivatives were obtained in good to excellent yields with high regioselectivity under constant current in an undivided cell equipped with carbon and platinum plates as the anode and cathode, respectively. Moreover, the convergent approach exhibited good functional group tolerance and could be easily scaled up
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Jurášek, Adolf, Vladimír Žvak, Jaroslav Kováč, Oľga Rajniaková та Jarmila Štetinová. "Synthesis and reactions of β-substituted derivatives of furan". Collection of Czechoslovak Chemical Communications 50, № 9 (1985): 2077–83. http://dx.doi.org/10.1135/cccc19852077.

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The 1,4-cycloaddition reaction of 4-phenyl-1,3-oxazole to 2-propinyl benzoate and dimethyl butinedioate afforded the respective 3-furylmethyl benzoate (I) and 3,4-bis(methoxycarbonyl)furan (II). These compounds served for the synthesis of 3-chloromethylfuran and 3,4-bis(chloromethyl)furan, which afforded via Wittig reaction 3-(β-arylvinyl)furans III (aryl = 5-nitro-2-furyl (IIIa), 5-nitro-2-thienyl (IIIb), 1-methyl-4-nitro-2-pyrrolyl (IIIc), and 4-nitrophenyl (IIIe)) and 3,4-bis(β-arylvinyl)furans IV (aryl = 5-nitrofuryl (IVa), 5-nitro-2-thienyl (IVc), and 4-nitrophenyl (IVd)). According to sp
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Saito, Yoshinori, Koji Takiguchi, Xun Gong, Chiaki Kuroda, and Motoo Tori. "Thiophene, Furans, and Related Aromatic Compounds from Eupatorium heterophyllum." Natural Product Communications 6, no. 3 (2011): 1934578X1100600. http://dx.doi.org/10.1177/1934578x1100600312.

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A thiophene, two furans, a dihydro furan, and two acetylenic benzene derivatives were isolated from the roots of Eupatorium heterophyllum collected in China. Structures were established on the basis of spectroscopic analyses as well as chemical transformations.
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Ma, Linyi, and Xuhui Jin. "Design of a novel D-A-D type furan-based charge transfer organic photoelectric material." Journal of Physics: Conference Series 2783, no. 1 (2024): 012025. http://dx.doi.org/10.1088/1742-6596/2783/1/012025.

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Abstract This work describes the synthesis of a novel D-A-D type furan derivative using a [2+2] cycloaddition and ring-opening reaction. Compared to thiophene-based materials, furan derivatives have lower aromaticity and more quinone-like structures, resulting in better π-electron delocalization. The novel D-A-D furan molecule in this paper exhibits a reduced bandgap and enhanced absorption in the near-infrared and visible regions, as well as strong fluorescence and good solubility.
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Lasseuguette, Elsa, Alessandro Gandini, and Hans-Joachim Timpe. "Photoreactive furan derivatives." Journal of Photochemistry and Photobiology A: Chemistry 174, no. 3 (2005): 222–28. http://dx.doi.org/10.1016/j.jphotochem.2005.03.012.

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Eggly, Alyssa S., Namuunzul Otgontseren, Carson B. Roberts, Amir Y. Alwali, Haylie E. Hennigan, and Elizabeth I. Parkinson. "A Diels–Alder probe for discovery of natural products containing furan moieties." Beilstein Journal of Organic Chemistry 20 (May 2, 2024): 1001–10. http://dx.doi.org/10.3762/bjoc.20.88.

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Natural products (NPs) are fantastic sources of inspiration for novel pharmaceuticals, oftentimes showing unique bioactivity against interesting targets. Specifically, NPs containing furan moieties show activity against a variety of diseases including fungal infections, and cancers. However, it is challenging to discover and isolate these small molecules from cell supernatant. The work described herein showcases the development of a molecular probe that can covalently modify furan moieties via a [4 + 2] Diels–Alder cycloaddition, making them easily identifiable on liquid chromatography–mass sp
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Dissertations / Theses on the topic "Furan derivatives"

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Yazicioglu, Emre Yusuf. "Transformation Of Cyclohexanone Derivatives To Bicyclic Furan And Pyrrole Derivatives." Master's thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/12605269/index.pdf.

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Tetrahydrobenzofurans and tetrahydroindoles are two very valuable classes of substances which have wide usage area<br>either as starting materials for drug substances or many other compounds which have fused heterocyclic rings in their structures and pharmacophore for many complex natural products<br>syntheses of derivatives of these compounds with different substitution patterns, is an exciting challenge for many scientists. Benzofuran and tetrahydroindole derivatives, which are potent bioactive substances, are synthesized from various cyclohexanone derivatives that are allylated by Stork-ena
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Livi, Francesco. "From 3,3,4,4-Tetraethoxybut-1-yne to furan derivatives." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2012. http://amslaurea.unibo.it/3004/.

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The starting material for this project was the highly functionalized compound 3,3,4,4- tetraethoxybut-1-yne (TEB) and it can be prepared from ethyl vinyl ether by a 4-steps synthesis. The third and the fourth step in TEB synthesis were sensitive to reaction conditions, so it was developed a strategy to try to optimize the third step and obtain TEB with higher yields. An approach, which tries to optimize also the fourth step, will be developed in further works. Several γ-hydroxy-α,β-unsaturated acetylenic ketones can be prepared from 3,3,4,4- tetraethoxybut-1-yne. TEB and γ-hydroxy-α,β-un
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Woollaston, Daniel. "Total synthesis of natural products via the oxidation of furan derivatives." Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.491599.

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Oxidation of furan rings in the presence of hydroxy groups can lead to spirobutenolides. This methodology has been applied in synthetic studies towards three natural products: Pyrenolide 0 - An antileukaemic fungal metabolite. AL-(1) - An antitumor plant natural product. Sawaranospirolides - Four highly oxygenated spiroacetals isolated from the heartwood of the Sawara tree.
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Gowda, Anitha Shankaralinge. "HYDROGENATION AND HYDROGENOLYSIS OF FURAN DERIVATIVES USING BIPYRIDINE-BASED ELECTROPHILIC RUTHENIUM(II) CATALYSTS." UKnowledge, 2013. http://uknowledge.uky.edu/chemistry_etds/29.

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The catalytic activity of ruthenium(II) bis(diimine) complexes cis-[Ru(6,6′-Cl2bpy)2(OH2)2](Z)2 (2, Z = CF3SO3; 3, Z = (3,5-(CF3)2C6H3)4B ,i.e. BArF), cis-[Ru(4,4′-Cl2bpy)2(OH2)2](Z)2 (4, Z = CF3SO3; 5, Z = BArF) and cis-[Ru(bpy)2(PR3)(OH2)](CF3SO3)2 (7, bpy = 2,2’-bipyridine, PR3 = P(C6H4F)3; 8, bpy = 2,2-bipyridine, PR3 = PPh3; 9, bpy = 4,4’-dichloro-2,2’-bipyridine, PR3 = PPh3; 10, bpy = 4,4’-dimethyl-2,2’-bipyridine, PR3 = P(C6H4F)3) for the hydrogenation and hydrogenolysis of furfural (FFR), furfuryl alcohol (FFA) and 5-hydroxymethylfurfural (HMF) was investigated. The compounds 2-5 are a
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Raffa, Guillaume. "Hétérocyclisations électrophiles et pallado-catalysées d’α-alcynyl β-alcoxyénones (et systèmes apparentés) : nouvelles voies d’accès à des dérivés furaniques tétrasubstitués". Thesis, Lyon 1, 2011. http://www.theses.fr/2011LYO10236.

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Banert, Klaus, Sandra Bochmann, Andreas Ihle, et al. "Synthesis with Perfect Atom Economy: Generation of Furan Derivatives by 1,3-Dipolar Cycloaddition of Acetylenedicarboxylates at Cyclooctynes." Universitätsbibliothek Chemnitz, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-152891.

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Cyclooctyne and cycloocten-5-yne undergo, at room temperature, a 1,3-dipolar cycloaddition with dialkyl acetylenedicarboxylates 1a,b to generate furan-derived short-lived intermediates 2, which can be trapped by two additional equivalents of 1a,b or alternatively by methanol, phenol, water or aldehydes to yield polycyclic products 3b–d, orthoesters 4a–c, ketones 5 or epoxides 6a,b, respectively. Treatment of bis(trimethylsilyl) acetylenedicarboxylate (1c) with cyclooctyne leads to the ketone 7 via retro-Brook rearrangement of the dipolar intermediate 2c. In all cases, the products are formed w
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Weber, Isabelle Kathrin [Verfasser], and M. [Akademischer Betreuer] Olzmann. "Kinetic Studies with Shock Tubes: Instrumental Developments and the Thermal Decomposition of Furan Derivatives / Isabelle Kathrin Weber ; Betreuer: M. Olzmann." Karlsruhe : KIT-Bibliothek, 2018. http://d-nb.info/1166234312/34.

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Hartmann, Ana Paula. "Síntese e avaliação de derivados furânicos, tetraidrofurânicos e pirrólicos com potencial atividade tripanocida." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/60/60138/tde-25092015-113957/.

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A Doença de Chagas é causada pelo Trypanosoma cruzi, e possui duas fases clínicas, sendo o tratamento com o fármaco benznidazol eficaz somente na fase aguda, porém com diversos efeitos adversos ao longo do período do tratamento. Desta forma, consórcios vêm sendo estabelecidos entre \"governo - universidade - indústria\", com auxilio de capital nacional e estrangeiro para o desenvolvimento de novos fármacos. Apesar de diversas ferramentas disponíveis para o planejamento de novos compostos, a busca por produtos naturais ainda desperta interesse de muitos pesquisadores. Diversos trabalhos vêm des
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Ulbrich, Kathrin [Verfasser], and Oliver [Akademischer Betreuer] Reiser. "The conversion of furan derivatives from renewable resources into valuable building blocks and their application in synthetic chemistry / Kathrin Ulbrich. Betreuer: Oliver Reiser." Regensburg : Universitätsbibliothek Regensburg, 2014. http://d-nb.info/1068055839/34.

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Benahmed-Gasmi, Amina. "Nouveaux précurseurs de matériaux organiques conducteurs : des donneurs-pi aux polymères conjugués." Angers, 1996. http://www.theses.fr/1996ANGE0020.

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Ce travail porte sur l'élaboration et la caractérisation de plusieurs séries de systèmes hybrides du tetrathiafulvalène (HTTFS). Ces systèmes sont construits par le greffage de deux motifs 1,3-dithiole-2-ylidene aux deux extrémités d'un espaceur conjugué. Apres une première étape consacrée à l'analyse des différentes possibilités d'insertion d'espaceurs benzéniques, plusieurs séries de HTTFS dérivées d'hétérocycles aromatiques, thiophène, furanne et n-méthyl pyrrole, ont été synthétisées, l'analyse des propriétés électrochimiques de ces derniers montre qu'ils conduisent à un abaissement du pot
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Books on the topic "Furan derivatives"

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Furans and Furan Derivatives - Recent Advances and Applications [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.95169.

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Asiri, Abdullah Mohammed, Anish Khan, and Mohammed Muzibur Rahman. Furan Derivatives: Recent Advances and Applications. IntechOpen, 2022.

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Lukevics, E., and L. M. Ignatovich. Organosilicon and Organo-Germanium Derivatives of Furan (Soviet Scientific Reviews Series, Section B). Routledge, 1988.

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Book chapters on the topic "Furan derivatives"

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Arican, Yagmur Emre. "Furan." In Food Safety. Nobel Tip Kitabevleri, 2024. http://dx.doi.org/10.69860/nobel.9786053358787.13.

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Furan, a volatile compound with a strong etheric odor and flammability, is a crucial component in the industrial context, producing various chemicals such as pyrrole, thiophene, tetrahydrofuran, pharmaceuticals, and pesticides. It is also used as a solvent for resins in organic synthesis and is present in many foods, including carbohydrates, unsaturated fatty acids, carotenoids, vitamin C, and amino acids, due to thermal processes and high-energy radiation used in the food manufacturing industry. Furan and its derivatives are utilized in the refining of tobacco and as flavoring agents in speci
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Boto, Alicia, and Laura Alvarez. "Furan and Its Derivatives." In Heterocycles in Natural Product Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634880.ch4.

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Aghazadeh, Ali, and Massoud Mahmoudian. "Different structural requirements for the inhibitory activity of furan carboxanilide derivatives against SDC for either wild or mutant strains of Ustilago maydis." In Trends in QSAR and Molecular Modelling 92. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1472-1_163.

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Wittich, Rolf-Michael. "Aerobic Degradation by Bacteria of Dibenzo-p-Dioxins, Dibenzofurans, Diphenyl Ethers and Their Halogenated Derivatives." In Biodegradation of Dioxins and Furans. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-662-06068-1_1.

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Golbs, S., M. Kuehnert, H. Zimmermann, and J. A. P. Donato. "Pharmacological-Toxicological Investigations with a Furan Derivative Produced from Sugar-Cane on Laboratory Animals." In Archives of Toxicology. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-74936-0_63.

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Guk Nam, Dong, Jung Woon Yang, and Do Hyun Ryu. "Catalytic Enantioselective Reactions of Biomass-Derived Furans." In Furans and Furan Derivatives - Recent Advances and Applications [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.101827.

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In this chapter, recent developments with regard to catalytic enantioselective reactions of furans, derived from biomass such as unsubstituted furan, 2-methylfuran, 2,5-dimethylfuran, and furfural are described. Although several review articles have dealt with the Diels-Alder reactions of furans, there have been no articles highlighting enantioselective versions. The resulting products derived from the catalytic enantioselective reaction of furan are often found as core structures in natural products and pharmaceuticals with important pharmacological activities. After recognizing the valuable
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Haider, N., and W. Holzer. "From Furan Derivatives." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00226.

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Pal, Pinki. "Recent advances in syntheses and antibacterial activity of novel furan derivatives." In Heterocyclic Chemistry - New Perspectives [Working Title]. IntechOpen, 2024. http://dx.doi.org/10.5772/intechopen.1004117.

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Microbial resistance has turned into a global issue due to the ineffectiveness of currently available antimicrobial medicines. In the realm of medicinal chemistry, furan derivatives have taken on a special position. An essential synthetic technique in the search for new drugs is the inclusion of the furan nucleus. Due to the remarkable therapeutic efficacy of furan-related medicines, medicinal chemists have been inspired to create numerous innovative antibacterial agents. Due to the numerous methods by which furans derivatives can be made as well as their numerous structural reactions, the fie
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Adelani Alabi, Kazeem, Rasheed Adewale Adigun, Ibrahim Olasegun Abdulsalami, and Mariam Dasola Adeoye. "Furfural: A Versatile Derivative of Furan for the Synthesis of Various Useful Chemicals." In Furan Derivatives - Recent Advances and Applications. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.100303.

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Furfural, a five-membered heterocyclic aromatic hydrocarbon derivable from acid hydrolysis of sugar cane bagasse, maize cob, rice husk or any cellulose-containing material, is useful in the synthesis of a range of specialized chemical products. Its condensation with nitromethane in basic medium yields 2-(2-Nitrovinyl) furan. This functional group (nitrovinyl) has been documented as a potent anti-microbial agent against gram-positive and gram-negative bacteria, with more potency against the gram-positive strains. The reaction of urea and thiourea with furfural yields bisimines-1,3-bis[(E)-furan
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Houssine Mabrouk, El. "Synthesis and Characterization of New Racemic α-Heterocyclic α,α-Diaminoester and α,α-Diamino Acid Carboxylic: 2-Benzamido-2-[(Tetrahydro-Furan-2-Ylmethyl)Amino]Acetate and 2-Benzamido-2-[(Tetrahydro-Furan-2-Ylmethyl)Amino] Acetic Acid." In Furan Derivatives - Recent Advances and Applications. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.98408.

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We reported here the synthesis of new α,α-diaminoester and α,α-diamino acid derivatives, as 2-benzamido-2-[(tetrahydro-furan-2-ylmethyl)amino] acetic acid through alkaline hydrolysis reaction of corresponding N-benzoylated methyl α,α-diamino ester. The α,α-diaminoester derivative was synthesized by nucleophilic substitution of methyl α-azido glycinate N-benzoylated with 2-tetrahydrofuran-2-ylmethan-amine. The structure of these products were established on the basis of NMR spectroscopy (1H, 13C), and MS data.
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Conference papers on the topic "Furan derivatives"

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Mih�ly, Norbert B., Miruna Prodan, Vasile M. Cristea, and Anton A. Kiss. "Sustainable Downstream Process Design for HMF Conversion to Value-Added Chemicals." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.185398.

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Biomass conversion to chemical derivatives and essential intermediates is regarded as a long-term strategy for the chemical sector. Among the numerous valuable chemicals obtained from biomass, 5-hydroxymethylfurfural (HMF) is considered an industrially relevant compound due to its capacity to be converted into a variety of value-added chemicals. Compared to conventional catalytic synthesis, bio-catalysis has emerged as a potential greener substitute for HMF conversion to value-added compounds. HMF conversion through bio-catalysis, although more sustainable, seldom leads to the production of a
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HENRIQUE FREIRE ARAUJO, LUIZ, José Augusto Rosário Rodrigues, FABIO NASARIO, and Paulo José Samenho Moran. "Biotransformation of Biomass Furan Derivatives." In XXIV Congresso de Iniciação Científica da UNICAMP - 2016. Galoa, 2016. http://dx.doi.org/10.19146/pibic-2016-51633.

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Kessler, Travis, Eric R. Sacia, Alexis T. Bell, and J. Hunter Mack. "Predicting the Cetane Number of Furanic Biofuel Candidates Using an Improved Artificial Neural Network Based on Molecular Structure." In ASME 2016 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/icef2016-9383.

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The next generation of alternative fuels is being investigated through advanced chemical and biological production techniques for the purpose of finding suitable replacements to diesel and gasoline while lowering production costs and increasing process yields. Chemical conversion of biomass to fuels provides a plethora of pathways with a variety of fuel molecules, both novel and traditional, which may be targeted. In the search for new fuels, an initial, intuition-driven evaluation of fuel compounds with desired properties is required. Due to the high cost and significant production time neede
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Fabian, Walter, Pedro Mancini, María Kneeteman, and Romina Brasca. "GLOBAL REACTIVITY INDEXES CALCULATED ON DIELSALDER PRIMARY ADDUCTS TO STUDY THE REGIO- AND STEREOCHEMISTRY OF THE REACTIONS BETWEEN FURAN DERIVATIVES AND DANISHEFSKY\'S DIENE." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00246.

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Lei, Hanwu, Shoujie Ren, James Julson, Lu Wang, Quan Bu, and Roger Ruan. "Microwave Torrefaction of Corn Stover and Tech-Economic Analysis." In ASME 2011 International Manufacturing Science and Engineering Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/msec2011-50230.

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Microwave torrefaction of corn stover with particle size of 4 mm was investigated and the effects of reaction temperature and time on the yields of volatile, bio-oil and torrefied biomass were determined. The response surface analysis of the central composite design (CCD) showed that the yields of volatile, bio-oil and torrefied biomass were significantly affected by the reaction temperature and time. Three linear models were developed to predict the yields of conversion products as a function of temperature and time. A first order reaction kinetics was also developed to model the corn stover
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Kinaci, Emre, Giuseppe Palmese, Joseph Stanzione, and Sarah Salazar. "Evaluation of hybridized bio-based building blocks as coating materials." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/oyjf3899.

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Commercial epoxy resins are often the oligomeric reaction products of bisphenol A (BPA) with epichlorohydrin. BPA is a toxic petrochemical and a well-known endocrine disruptor which can mimic the body’s own hormones and may lead to several negative health effects. The most common curing agents are also the derivatives of toxic amines such as aniline, ethylene di-amine, and ammonia etc. which are under strict regulations and restrictions by TSCA and (REACH) agencies. Therefore; there is a growing demand to develop epoxy and amine systems from non- or less- toxic and annually renewable precurs
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Hannis Fadzillah Mohsin, Ibtisam Abdul Wahab, and Jean-Frederic Faizal Weber Abdullah. "A derivative of furan-2,3-diol from pandan extract." In 2010 International Conference on Science and Social Research (CSSR). IEEE, 2010. http://dx.doi.org/10.1109/cssr.2010.5773758.

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Kiruthika, M., and M. Srinivasan. "Antioxidant potential against furan derivative in natural ester based insulating fluid." In 2017 4th International Conference on Innovations in Information, Embedded and Communication Systems (ICIIECS). IEEE, 2017. http://dx.doi.org/10.1109/iciiecs.2017.8275924.

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