Relevant bibliographies by topics / Cyclohexenone

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

Academic literature on the topic 'Cyclohexenone'

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

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Journal articles on the topic "Cyclohexenone"

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El-Korso, Sanaa, Sumeya Bedrane, Abderrahim Choukchou-Braham, and Redouane Bachir. "The effect of redox properties of ceria-supported vanadium oxides in liquid phase cyclohexene oxidation." RSC Advances 5, no. 78 (2015): 63382–92. http://dx.doi.org/10.1039/c5ra11430f.

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In the presence of redox catalysts, cyclohexene oxidation leads to an epoxidation product, while in the presence of acidic features; the allylic oxidation is predominant and leads to cyclohexenol and cyclohexenone.
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S., Khare, та Shrivastava S. "Epoxidation of cyclohexene catalysed by MnII supported on α-titanium arsenate as catalyst and dry TBHP as an oxidant". Journal of Indian Chemical Society Vol. 83, Aug 2006 (2006): 813–18. https://doi.org/10.5281/zenodo.5827777.

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School of Chemical Sciences, Takshashila Campus, Khandwa Road, Devi Ahilya University, Indore-452 017, Madhya Pradesh, India <em>E-mail</em> : kharesavita@rediffmail.com <em>Manuscript received 5 August 2005, revised 10 May 2006. accepted 16 May 2006</em> Manganese supported on a-titanium arsenate {&alpha;-TiMn<sup>II</sup>As} was synthesized by ion-exchange method and characterized by DSC. Its catalytic activity is reported for cpoxidation of cyclohexene using dry tert-butylhydroperoxide (TBHP) as an oxidant.In the epoxidation reaction&nbsp;cyrlohexene was oxidized to cyclohexene oxide,cycloh
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Chen, Jingwen, Minda Chen, Biying Zhang, et al. "Allylic oxidation of olefins with a manganese-based metal–organic framework." Green Chemistry 21, no. 13 (2019): 3629–36. http://dx.doi.org/10.1039/c9gc01337g.

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Hylden, Anne T., Eric J. Uzelac, Zeljko Ostojic, et al. "Cyclization of 5-hexynoic acid to 3-alkoxy-2-cyclohexenones." Beilstein Journal of Organic Chemistry 7 (September 23, 2011): 1323–26. http://dx.doi.org/10.3762/bjoc.7.155.

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The one-pot cyclization of 5-hexynoic acid to produce 3-alkoxy-2-cyclohexenones proceeds in good yields (58–90%). 3-Hexynoic acid was converted to its acyl chloride with the aid of oxalyl chloride and was cyclized to 3-chloro-2-cyclohexenone upon addition of indium(III) chloride. Subsequent addition of alcohol nucleophiles led to the desired 3-alkoxy-2-cyclohexenones.
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Fujii, Tatsuya, Tomohiro Ozawa, Yasuhiro Funahashi, Koichiro Jitsukawa, and Hideki Masuda. "Synthesis of Mononuclear Non-Heme Iron(III)-Hydroperoxo Complex as an Oxidative Catalyst." Advanced Materials Research 11-12 (February 2006): 331–34. http://dx.doi.org/10.4028/www.scientific.net/amr.11-12.331.

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Mononuclear FeII complex [FeII(ppba)]2+ (ppba = (6-pivalamido-2-pyridylmethyl) (2-pyridylmethyl)tert-butylamine) (1) has been synthesized and structurally characterized. The addition of H2O2 (10eq) to an acetone solution of 1 at -78°C generated FeIIIPPBA-OOH species, accompanied by a color change from pale yellow to reddish purple, which showed an intense absorption band corresponding to LMCT band (HOO- to Fe) at 528 nm (ε = 1120 M-1cm-1). The ESR spectrum for FeIIIPPBA-OOH species (g// = 4.22, g⊥ = 7.70 in acetone at 77 K) was typical of a high-spin FeIII species, suggesting that the FeIIIPPB
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Weir, D., J. C. Scaiano, and D. I. Schuster. "A reinvestigation of the interaction between triplet states of cyclohexenones and amines." Canadian Journal of Chemistry 66, no. 10 (1988): 2595–600. http://dx.doi.org/10.1139/v88-407.

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Laser flash photolysis studies lead to the conclusion that the short-lived triplet states of cyclohexenones are readily quenched by amines. For example, in the case of 2-cyclohexen-1-one (1) its triplet state (τT = 40 ns in acetonitrile) is quenched by triethylamine with a rate constant of (9.0 ± 0.8) × 107 M−1 s−1. Cyclohexenone triplets are also quenched efficiently by DABCO and by triphenylamine leading to the formation of the corresponding amine radical cations. The new evidence reported rules out the involvement of long-lived detectable exciplexes.
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Schuster, David I., Jie-Min Yang, Jan Woning, Timothy A. Rhodes, and Anton W. Jensen. "Mechanism of acid-catalyzed photoaddition of methanol to 3-alkyl2-cyclohexenones." Canadian Journal of Chemistry 73, no. 11 (1995): 2004–10. http://dx.doi.org/10.1139/v95-247.

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Contrary to a previous report, it is concluded that formation of methanol adducts to 3-methyl-2-cyclohexenones and of deconjugated enones on irradiation of the enones in acidified solutions proceeds via protonation of the intermediate enone π,π* triplet excited state and not by protonation of a relatively long-lived ground state trans-cyclohexenone. A rate constant for protonation of the triplet state of 3-methyl-2-cyclohexenone by sulfuric acid of 1.7 × 109 M−1 s−1 was determined by laser flash photolysis in ethyl acetate. Based on quantum efficiencies of product formation, a rate constant of
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Atioğlu, Zeliha, Mehmet Akkurt, Flavien A. A. Toze, Gunay Z. Mammadova, and Humay M. Panahova. "Crystal structure and Hirshfeld surface analysis of 3,3′,3′′-[(1,3,5-triazine-2,4,6-triyl)tris(oxy)]tris(5,5-dimethylcyclohex-2-en-1-one)." Acta Crystallographica Section E Crystallographic Communications 74, no. 7 (2018): 1035–38. http://dx.doi.org/10.1107/s2056989018009003.

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The three cyclohexenone rings of the title compound, C27H33N3O6, adopt slightly distorted envelope conformations, with the C atom bearing two methyl groups as the flap atom in each case. These cyclohexenone mean planes form dihedral angles of 87.41 (11), 70.73 (11) and 70.47 (11)° with the 1,3,5-triazine ring, while the dihedral angle between the cyclohexenone mean planes are 57.52 (12), 23.75 (12) and 53.21 (12)°. In the crystal, molecules are linked via C—H...O hydrogen bonds, forming a three-dimensional network.
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Sureshbabu, N., and V. Sughanya. "6-Hydroxy-5-[(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)(4-nitrophenyl)methyl]-1,3-dimethylpyrimidine-2,4(1H,3H)-dione." Acta Crystallographica Section E Structure Reports Online 69, no. 11 (2013): o1690—o1691. http://dx.doi.org/10.1107/s1600536813028584.

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In the title compound, C21H23N3O7, the pyrimidinedione ring adopts a screw-boat conformation, whereas the cyclohexenone ring adopts an envelope conformation, with the C atom bearing the methyl groups as the flap atom. The dihedral angle between the mean planes of the pyrimidinedione and cyclohexenone rings is 58.78 (2)°. The pyrimidinedione and cyclohexenone rings form dihedral angles of 59.94 (3) and 54.73 (2)°, respectively, with the 4-nitrophenyl ring. Relatively strong intramolecular O—H...O hydrogen bonds are observed. In the crystal, molecules are linked by C—H...O hydrogen bonds, formin
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Leepasert, Theerachart, Patchreenart Saparpakorn, Kittipong Chainok, and Tanwawan Duangthongyou. "Crystal structure of 5-[(benzoyloxy)methyl]-5,6-dihydroxy-4-oxocyclohex-2-en-1-yl benzoate." Acta Crystallographica Section E Crystallographic Communications 76, no. 7 (2020): 1096–100. http://dx.doi.org/10.1107/s2056989020007793.

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The crystal structure of the natural product zeylenone, C21H18O7, was confirmed by single-crystal X-ray diffraction. The crystal structure has three chiral centers at positions C1, C5 and C6 of the cyclohexanone ring, but the absolute configuration could not be determined reliably. The methyl benzoate and benzoyloxy substituents at positions C1 and C5 of the cyclohexenone ring are on the same side of the ring with the dihedral angle between their mean planes being 16.25 (10)°. These rings are almost perpendicular to the cyclohexenone ring. The benzoate groups and two hydroxyl groups on the cyc
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Dissertations / Theses on the topic "Cyclohexenone"

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Ohnemüller, Ulrike. "Effiziente Synthese hochsubstituierter enantiomerenreiner Cyclohexenone und Tetrahydroxanthenone." Berlin Logos-Verl, 2005. http://deposit.ddb.de/cgi-bin/dokserv?id=2793052&prov=M&dok_var=1&dok_ext=htm.

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Ohnemüller, Ulrike Kerstin. "Effiziente Synthese hochsubstituierter enantiomerenreiner Cyclohexenone und Tetrahydroxanthenone /." Berlin : Logos Verl, 2006. http://deposit.ddb.de/cgi-bin/dokserv?id=2793052&prov=M&dok_var=1&dok_ext=htm.

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Jaunet, Alex. "Synthetic approaches to naturally occuring cyclohexenone epoxides." Thesis, University of Sheffield, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.505527.

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Chen, Jianxin. "A study of the photorearrangements of crystalline dibenzobarrelene and cyclohexenone derivatives." Thesis, University of British Columbia, 1991. http://hdl.handle.net/2429/30985.

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Two series of compounds, 4,4-diarylcyclohexenones and 9-substituted dibenzobarrelenes, were synthesized and their photochemistry was investigated in the crystalline state and in solution medium. The differences in photoreactivity and product selectivity of these compounds between the solution and solid states have been determined, and possible structure-reactivity correlations are discussed based on X-ray crystallographic data for some of the substances. The photorearrangement of 4,4-diarylcyclohexenones was found to be affected moderately by the crystal lattice. The migratory aptitude of the
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Hwang, Christine. "Crystal structures and solid state reactions of maleic anhydride and of a cyclohexenone and its photoproduct." Thesis, University of British Columbia, 1988. http://hdl.handle.net/2429/27966.

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Two sets of structures were determined by X-ray crystallographic techniques, one of maleic anhydride (2,5-furandione) and the other of 4-phenyl-4-p-bromophenylcyclohex-2-en-1-one and its photoproduct, trans-5-phenyl-6-p-bromophenylbicyclo[3.1.0]hexan-2-one. Analysis of maleic anhydride included a room temperature redetermination of the crystal structure. This was done to improve parameters and simplify comparison of the room temperature and low temperature data. The structure determination at 104k resulted in the location of bonding electrons in the double bond. Thermal motions of both sets o
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Boulet, Serge L. "Total syntheses of (±)-neoverrucosan-5(ß)-ol, (±)-homoverrucosan-5(ß)-ol, (±)-verrucosan-2(ß)-ol, and (±)-(3R,4R, 5R, 6S, 9R)-cyatha-12, 18-diene, a new cyclohexenone annulation sequence." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ34515.pdf.

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Xing, Dongxia. "Stereoselective Solid-State NaBH₄ Reduction of 1-Methylpentacyclo[5.4.0.0²,⁶.0³,¹⁰,0⁵,⁹]undecane-8, 11-Dione, Synthesis and Chemistry of Strained Alkenes, and Chemical and Microbial Synthesis of Racemic and Optically Active (S)-4-Hydroxy-2-Cyclohexenone." Thesis, University of North Texas, 1995. https://digital.library.unt.edu/ark:/67531/metadc278368/.

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Part I. Reduction of the 1-methylpentacyclo [5.4.0.0²,⁶.0³,¹⁰,0⁵,⁹]undecane-8, 11-dione (9) with solid NaBH₄ resulted in highly stereoselective reduction of both C=O groups in the substrate, thereby affording the corresponding endo-8, endo-11-diol (11a). The configuration of 11a was established unequivocally by converting 11a into the corresponding cyclic thiocarbonate ester, 12. Part II. Z-1,2-Di(1'-adamantyl)ethene (14) was synthesized with a high degree of stereoselectively in four steps (Scheme 9 in Chapter 2). E-1,2-di(1'-adamantyl)ethene (15) was synthesized by iodine promoted isomerizat
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Hookins, Daniel Ritchie. "Synthesis of oxygenated cyclohexene natural products." Thesis, University of York, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.547340.

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Adesina, Olumide, Cassandra T. Eagle, Ayobami Olukanni, and Reza Mohseni. "Purification of Cyclohexene for Cyclopropanation Reactions." Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/asrf/2019/schedule/143.

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Environmentally friendly reactions yielding cis-cyclopropanes are desired in the insecticide industry as these are most effective at reducing the population of insects while remaining benign to the environment. We are exploring the best parameters for the most effective cis-cyclopropanation reactions. An alkene and a diazo compound react together in the presence of a dirhodium catalyst to produce cyclopropanes. First however, the starting materials must be pure. Alfa Aesar supplies cyclohexene which is reported to be 99% pure, however, Gas column chromatography/Mass spectroscopy reveals that t
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Clark, R. S. J. "The synthesis of cyclohexenones by rearrangement of bicyclo(2,2,2)octanones." Thesis, University of Cambridge, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.356675.

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Books on the topic "Cyclohexenone"

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. 4-biniru-1-shikurohekisen: 4-vinyl-1-cyclohexene. Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2009.

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Liu, Zhongyi, Shouchang Liu, and Zhongjun Li. Catalytic Technology for Selective Hydrogenation of Benzene to Cyclohexene. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-6411-6.

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Begin, Paul. Terpolymerization of cyclohexene, 3-butenoic acid and sulfur dioxide. Laurentian University, 1986.

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Moralee, Andrew Charles. The synthesis of geminally difluorinated cyclohexenols via Diels-Alder chemistry. University of Birmingham, 2001.

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Georgiades, George Chris. A study of cyclohexene reactions on supported characterised metal catalysts. Brunel University, 1988.

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Su, Ping. Copolymerization characteristics of sulfur dioxide and cyclohexene: Initiation/termination mechanism by end group analysis. s.n.], 1987.

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Chhabra, Rajendra. NTP technical report on the toxicology and carcinogenesis studies of 4-vinyl-1-cyclohexene diepoxide (CAS no. 106-87-6) in F344/N rats and B6C3F1 mice (dermal studies). National Toxicology Program, U. S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 1989.

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Chhabra, Rajendra. NTP technical report on the toxicology and carcinogenesis studies of 4-vinyl-1-cyclohexene diepoxide (CAS no. 106-87-6) in F344/N rats and B6C3F ́mice (dermal studies). U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 1989.

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Li, Zhongjun, Zhongyi Liu, Shouchang Liu, and Wang Erqiang. Catalytic Technology for Selective Hydrogenation of Benzene to Cyclohexene. Springer, 2020.

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Catalytic Technology for Selective Hydrogenation of Benzene to Cyclohexene. Springer Singapore Pte. Limited, 2021.

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Book chapters on the topic "Cyclohexenone"

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Gooch, Jan W. "Cyclohexene Oxide." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3242.

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Lide, David R. "117. Cyclohexene." In Handbook of Organic Solvents. CRC Press, 2024. http://dx.doi.org/10.1201/9781003575191-108.

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Wohlfarth, Christian. "Refractive index of cyclohexene." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_223.

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Mahidol, Chulabhorn. "Naturally Occurring Cyclohexene Epoxides Revisited." In Ciba Foundation Symposium 154 - Bioactive Compounds from Plants. John Wiley & Sons, Ltd., 2007. http://dx.doi.org/10.1002/9780470514009.ch6.

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Bährle-Rapp, Marina. "2,4-Dimethyl-3-Cyclohexene Carboxaldehyde." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3119.

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Winkelmann, J. "Diffusion of hydrogen (1); cyclohexene (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1541.

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Winkelmann, Jochen. "Diffusion coefficient of cyclohexene in cyclohexane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_543.

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Winkelmann, Jochen. "Diffusion coefficient of cyclohexene in octane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_544.

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Winkelmann, Jochen. "Diffusion coefficient of cyclohexene in decane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_545.

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Winkelmann, Jochen. "Diffusion coefficient of cyclohexene in dodecane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_546.

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Conference papers on the topic "Cyclohexenone"

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Wisetsai, A., R. Lekphrom, and FT Schevenels. "Roxydienone, a novel cyclohexenone from Trachyspermum roxburghianum." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3400153.

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Peng, Hui-Sheng, and Tian-Hang Yang. "Flame Propagation Characteristic of Cyclohexene/Air Mixtures." In AIAA AVIATION 2023 Forum. American Institute of Aeronautics and Astronautics, 2023. http://dx.doi.org/10.2514/6.2023-3786.

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Kukolich, Stephen, Shih-Yuan Liu, Jacob Ishibashi, Adam Daly, and Ming Sun. "IDENTIFICATION AND CHARACTERIZATION OF 1,2-BN CYCLOHEXENE USING MICROWAVE SPECTROSCOPY." In 71st International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.wk01.

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Bezborodov, Vladimir, Roman S. Dabrowski, Genadz Sasnouski, V. Lapanik, and Jerzy Dziaduszek. "New LC cyclohexene and cyclohexane derivatives: LC compositions on their base." In XIV Conference on Liquid Crystals, Chemistry, Physics, and Applications, edited by Jolanta Rutkowska, Stanislaw J. Klosowicz, and Jerzy Zielinski. SPIE, 2002. http://dx.doi.org/10.1117/12.472203.

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Liu, Xue, Ling Zhang, Wei-Qiao Deng, and Nian-Yu Huang. "Mn-, Ru-Coordinated Covalent Triazine Framework as Catalysts for Epoxidation of Cyclohexene." In 2015 Asia-Pacific Energy Equipment Engineering Research Conference. Atlantis Press, 2015. http://dx.doi.org/10.2991/ap3er-15.2015.26.

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Sonstrom, Reilly, Brooks Pate, W. Harman, Jacob Smith, and Patrick Kelleher. "ISOTOPOLOGUE AND ISOTOPOMER ANALYSIS OF DEUTERATED CYCLOHEXENE USING MOLECULAR ROTATIONAL RESONANCE SPECTROSCOPY." In 2020 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.fc04.

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Tykarski, W., Jerzy Dziaduszek, Roman S. Dabrowski, and Vladimir Bezborodov. "Synthesis and mesogenic properties of compounds with lateral substituted cyclohexane and cyclohexene ring." In Liquid Crystals, edited by Marzena Tykarska, Roman S. Dabrowski, and Jerzy Zielinski. SPIE, 1998. http://dx.doi.org/10.1117/12.301314.

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Petrovic, Zoran, Dragana Radojcic, and Jian Hong. "Epoxy materials with triglyceride structure." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/jegt5242.

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Preparing materials for technical applications made completely from natural oils is always a respectable goal. Epoxidized oils are an excellent platform for a range of new polymers, including cross-linked epoxy resins prepared by cationic ring-opening polymerization. Casts of glassy or rubbery epoxy resins were made from epoxidized algal, soybean, and linseed oils at room temperature, in relatively short amounts of time. The tris(pentafluorophenyl)borane catalyst allowed for precise control of the processing time and curing temperature, even at very low concentrations. Properties of the resi
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Otto, Jessica, Evan Davison, and Randy Maglinao. "Synthesis of Cycloalkanes from Lignocellulosic Platform." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/qbeo2379.

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Abstract: Catalytic hydrodeoxygenation of biooil is instrumental in producing sustainable aviation fuels, specifically cycloalkanes, from lignocellulosic materials. Cycloalkanes typically have higher energy densities, lower freeze points and higher flash points than conventional jet fuel. In our study, we compared hydrodeoxygenation of p-cresol using Pd/C and tandem hydrogenation-dehydration using Pd/C for hydrogenation and heteropolyacid on alumina catalyst for dehydration. All of the hydrodeoxygenation and hydrogenation trials were ran at 250°C and 600 psi of hydrogen gas while dehydration t
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Aliaj, Fisnik, Naim Syla, and Arlinda Bytyqi-Damoni. "Refractive indices of cyclohexene + ethanol + acetone ternary system at T = (293.15, 298.15 and 303.15) K and atmospheric pressure." In The 3rd Virtual Multidisciplinary Conference. Publishing Society, 2015. http://dx.doi.org/10.18638/quaesti.2015.3.1.249.

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