Academic literature on the topic 'Trimethylphenol'

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Journal articles on the topic "Trimethylphenol"

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Nazarova, M., and I. Mammadzadeh. "SYNTHESIS OF TRIMETHYLPHENOLS IN THE CATALYTIC ALKYLATION OF XYLENOL AND METHANOL AND APPLICATION IN THE PRODUCTION OF VITAMIN E (TOCOPHEROL)." Slovak international scientific journal, no. 92 (February 14, 2025): 4–6. https://doi.org/10.5281/zenodo.14869675.

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In this article, the alkylation reactions of 2,6-, 2,5- and 2,3-dimethylphenols in the presence of methanol and CrCaY zeolite were investigated. The experiments were carried out at a temperature of 360°C and a volume flow rate of 0.82 st·¹. The results show that, regardless of the catalyst composition, the main conversion product of 2,6-dimethylphenol is 2,4,6-trimethylphenol. In the presence of CrCaY zeolite, 2,3,6-trimethylphenol is also formed with some selectivity. The potential application of trimethylphenols obtained in the alkylation process in the synthesis of tocophero
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Ziemer, Burkhard, and Oxana Surygina. "2,4,6-Trimethylphenol." Acta Crystallographica Section C Crystal Structure Communications 56, no. 11 (2000): e528-e528. http://dx.doi.org/10.1107/s0108270100013524.

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Gordon, JLM, MP Hartshorn, RJ Martyn, AJ Morgan, WT Robinson, and GJ Wright. "The Chlorination of Some Substituted 2,4-Dimethylphenols." Australian Journal of Chemistry 47, no. 2 (1994): 289. http://dx.doi.org/10.1071/ch9940289.

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Chlorination reactions of 2-chloro-3,4,6-trimethylphenol (4), 2-chloro-4,6-dimethylphenol (5) and 3-chloro-2,4,6-trimethylphenol (6) are described. In acetic acid or acetic anhydride solution, chlorinations yield predominantly the corresponding 4-chlorocyclohexa-2,5-dienones (8), (17a) and (29), but in carbon tetrachloride containing pyridine products are formed which result from the modification of the 4-methyl group in each substrate. X-Ray crystal structure analyses are reported for compounds (7), (14), (28) and (31).
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Hartshorn, MP, KA Hayman, RJ Martyn, et al. "The Chlorination of 4-Chloro-2,3,6-trimethylphenol. Some Addition-Reactions of 4,6-Dichlorocyclohexa-2,4-dienones." Australian Journal of Chemistry 43, no. 10 (1990): 1729. http://dx.doi.org/10.1071/ch9901729.

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Reaction of a mixture of 6-chlorocyclohexa-2,4-dienones (4) and (5) with chlorine in acetic acid gives the tetrachloro ketones (2) and (3), the major products of chlorination of 2,3,6-trimethylphenol (1a) or 4-chloro-2,3,6-trimethylphenol (1b). Reactions of this mixture of 6- chlorocyclohexa-2,4-dienones (4) and (5) in acetic acid with chlorine acetate, chlorine, chlorine in the presence of sodium acetate, and in benzene with nitrogen dioxide are described. -Ray crystal structure determinations are reported for compounds (3), (6)-(8) and (11)-(13).
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Гребенникова, Ольга Валентиновна, Александрина Михайловна Сульман, Степан Петрович Михайлов, Елена Игоревна Шиманская, and Валентина Геннадьевна Матвеева. "OXIDATION OF ORGANIC COMPOUNDS BY MAGNETIC BIOCATALYST." Вестник Тверского государственного университета. Серия: Химия, no. 1(39) (March 19, 2020): 31–39. http://dx.doi.org/10.26456/vtchem2020.1.4.

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В статье описывается синтез магнитного биокатализатора на основе иммобилизованной пероксидазы. Данный биокатализатор тестировался в реакции окисления 2,3,6-триметилфенола с помощью пероксида водорода до 2,3,5-триметилгидрохинона (полупродукта витамина Е). В работе выбран метод синтеза магнитных наночастиц. Подобраны оптимальные условия проведения процесса окисления 2,3,6-триметилфенола в присутствии магнитного биокатализатора (начальная концентрация субстрата, температура, рН). The article describes the synthesis of a magnetic biocatalyst based on immobilized peroxidase. This biocatalyst was t
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Гребенникова, Ольга Валентиновна, Александрина Михайловна Сульман, Владимир Петрович Молчанов, Елена Михайловна Михайлова, Ирина Павловна Шкилева, and Валентина Геннадьевна Матвеева. "STUDY OF THE KINETICS OF ENZYMATIC OXIDATION OF 2,3,6-TRIMETHYLPHENOL IN THE PRESENCE OF IMMOBILIZED PEROXIDASE." Вестник Тверского государственного университета. Серия: Химия, no. 4(42) (December 21, 2020): 7–15. http://dx.doi.org/10.26456/vtchem2020.4.1.

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В работе изучался процесс окисления 2,3,6-триметилфенола в присутствии иммобилизованной пероксидазы корня хрена. В результате такого окисления был получен полупродукт витамина Е (2,3,5-триметилгидрохинон). Иммобилизация фермента проводилась на магнитные наночастицы, на SiO и AlO. Все исследованные биокатализаторы показали стабильную работу в процессе окисления 2,3,6-триметилфенола с помощью пероксида водорода. Таким образом, синтезированные биокаталитические ферментные системы могут успешно применяться в качестве альтернативных катализаторов окисления замещенных фенолов с целью получения биоло
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Saux, Clara, Luis R. Pizzio, and Liliana B. Pierella. "2,3,5-Trimethylphenol oxidation over Co-based solid catalysts." Applied Catalysis A: General 452 (February 2013): 17–23. http://dx.doi.org/10.1016/j.apcata.2012.11.037.

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Li, Kuo-Tseng, and Pang-Yih Liu. "Oxidation of 2,4,6-trimethylphenol using iron-based catalysts." Applied Catalysis A: General 272, no. 1-2 (2004): 167–74. http://dx.doi.org/10.1016/j.apcata.2004.05.038.

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Shen, Yu, Fumin Wang, Chaoqun Yang, and Xubin Zhang. "Synthesis and Characterisation of Hierarchically Porous HZSM-5 as Catalysts for the Synthesis of 2,3,5-Trimethyl-1,4-benzoquinone." Australian Journal of Chemistry 70, no. 6 (2017): 691. http://dx.doi.org/10.1071/ch16392.

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Hierarchical HZSM-5 were synthesised by controlled desilication in alkaline medium and characterised by field-emission scanning electron microscopy, X-ray diffraction, transmission electron microscopy, inductively coupled plasma–atomic emission spectrometry, N2 adsorption–desorption, and Fourier transform infrared spectroscopy. The catalytic performance of HZSM-5 towards the selective oxidation of 2,3,6-trimethylphenol by H2O2 was evaluated. Recyclability tests were also carried out. The results showed that 2,3,5-trimethyl-1,4-benzoquinone was produced in high yields (i.e. 90 %), corresponding
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Chambers, MV, MP Hartshorn, WT Robinson, and J. Vaughan. "The Nitration of 2,3,4-Tribromo-5,6-dimethylphenol and 3,4-Dibromo-2,5,6-trimethylphenol." Australian Journal of Chemistry 38, no. 1 (1985): 133. http://dx.doi.org/10.1071/ch9850133.

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The nitrations of 2,3,4-tribromo-5,6-dimethylphenol (9) and 3,4- dibromo-2,5,6-trimethylphenol (10) with fuming nitric acid in acetic acid give 2,5,6-trinitrocyclohex-3-enones in addition to 6-hydroxy-2,5-dinitrocyclohex-3-enones. X-ray crystal structure determinations are reported for the trinitro ketones (21) and (22), and the hydroxy dinitro ketones (23) and (24).
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Dissertations / Theses on the topic "Trimethylphenol"

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Cawley, Kaelin Marie. "The sensitized photolysis of 2,4,6-Trimethylphenol, Atrazine and Metolachlor in a temperate Eutrophic wetland." The Ohio State University, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=osu1406647483.

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Chatwin, Sarah Louise. "Ruthenium hydride complexes bearing the ligand 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene." Thesis, University of Bath, 2007. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.443541.

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Chang, Ching-Hsiang, and 張清香. "Synthesis of Certain New Dienes from Naphthol and 2,3,5-Trimethylphenol." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/94448889331516218415.

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碩士<br>高雄醫學大學<br>醫藥暨應用化學系碩士班<br>93<br>In this master thesis the synthesis of 1-allyloxy-2-(2-methylallyl)- naphthalene and 1-allyloxy-2-(2-phenylallyl)naphthalene from naphthol is described. On the other hand,synthesis of 3-allyloxy-1,2,5-trimethyl-4-(2- methylallyl)benzene and 3-allyloxy-1,2,5-trimethyl-4-(2-phenylallyl) benzene from 2,3,5- trimethylphenol, is also described. Naphthol or 2,3,5- trimethylphenol dissolved in anhydrous acetone was respectively reacted with 1-chloroacetone and 2-bromoacetophenone in refluxing acetone in the presence of K2CO3 to undergo SN2 reaction to give carbony
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Tsai, Chia Lung, and 蔡佳龍. "Synthesis of Novel Molecular Sieves and Studies on Catalytic Oxidation of Trimethylphenol over Cu,Al-MCM-41." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/11713136081488482950.

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Prokofieva, Angelina. "Bioinspired oxidation reactions of phenols with dinuclear copper complexes." Doctoral thesis, 2007. http://hdl.handle.net/11858/00-1735-0000-000D-F12D-0.

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Book chapters on the topic "Trimethylphenol"

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Tan, Robin P., Gregory R. Gillette, Howard B. Yokelson, Robert West, and Philip Boudjouk. "Tetrakis (2,4,6-Trimethylphenyl)Disilene (Tetramesityldisilene)." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132609.ch8.

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Winkelmann, Jochen. "Diffusion coefficient of bis(2,4,4-trimethylphenyl)-phosphinic acid in tetrachloro-methane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_1092.

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Winkelmann, Jochen. "Diffusion coefficient of bis(2,4,4-trimethylphenyl)-phosphinic acid in trichloro-deuterio-methane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_1091.

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"Trimethylphenyl-ammonium chloride." In Toxicological Evaluations. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-84195-8_18.

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Takehira, Katsuomi, Masao Shimizu, Yoshihito Watanabe, Hideo Orita, and Takashi Hayakawa. "A Novel and Effective Oxygenation of 2,3,6-Trimethylphenol To Trimethyl-p-Benzoquinone by Dioxygen with Copper(II) Chloride/Amine Hydrochloride System Catalyst." In New Developments in Selective Oxidation. Elsevier, 1990. http://dx.doi.org/10.1016/s0167-2991(08)60142-1.

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Echavarren, A. M., and S. Porcel. "Oxidative Dimerization of 2,4,6-Trimethylphenyl Chloroformate." In Quinones and Heteroatom Analogues. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-028-00538.

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"2,4,6-Tri-tert.-butylphenylphosphane, (E)-1,2-Bis(2,4,6-tri-tert.-butylphenyl)diphosphene, (E)-1-(2,4,6-Trimethylphenyl)-2-(2,4,6-tri-tert.-butylphenyl)diphosphene." In Phosphorus, Arsenic, Antimony and Bismuth, edited by Karsch. Georg Thieme Verlag, 1996. http://dx.doi.org/10.1055/b-0035-114102.

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Conference papers on the topic "Trimethylphenol"

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Liu, Wei, Ying Li, Pei Zhang, et al. "Hypocrellin B graft on activated carbon and photocatalytic oxidation of 2,3,5-trimethylphenol." In Photonics and Optoelectronics Meetings, edited by Qingming Luo, Lihong V. Wang, and Valery V. Tuchin. SPIE, 2008. http://dx.doi.org/10.1117/12.821175.

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Grebennikova, Olga, Aleksandrina Sulman, Elena Shimanskaya, Esther Sulman, and Valentin Doluda. "ENZYMATIC KINETICS OF THE OXIDATION OF 2,3,6-TRIMETHYLPHENOL IN THE PRESENCE OF IMMOBILIZED PEROXIDASE." In 20th International Multidisciplinary Scientific GeoConference Proceedings SGEM 2020. STEF92 Technology, 2020. http://dx.doi.org/10.5593/sgem2020/6.1/s25.032.

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ZHANG, PEI, YING LI, WEI LIU, et al. "A HIGHLY SELECTIVE PHOTOOXIDATION OF 2,3,5-TRIMETHYLPHENOL TO 2,3,5-TRIMETHYLBENZOQUINONE USING HYPOCRELLINS AS CATALYSTS." In Proceedings of the 6th International Conference on Photonics and Imaging in Biology and Medicine (PIBM 2007). WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812832344_0033.

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Roslan, Nurliana, Salasiah Endud, Zainab Ramli, and Mohd Bakri Bakar. "Synthesis of ionic liquid-functionalized mesoporous SBA-15 containing copper porphyrin for oxidation of trimethylphenol." In INTERNATIONAL CONFERENCE ON RECENT TRENDS IN COMPOSITE SCIENCES WITH COMPUTATIONAL ANALYSIS. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0185631.

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Vita, Diana E., Mercedes A. Badajoz, Marcos J. Lo Fiego, and Gustavo F. Silbestri. "Synthesis of N-Heterocyclic Carbene Gold Complexes Using 2,4,6-Trimethylphenyl Sydnone as Model Substrate †." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13674.

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