Relevant bibliographies by topics / Trimethoxyphenol

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

Academic literature on the topic 'Trimethoxyphenol'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Trimethoxyphenol"

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Jia, Xiao-Chuan, Jing Li, Zhi-Rui Yu, Hui Zhang, and Lei Zhou. "3,4,5-Trimethoxyphenol." Acta Crystallographica Section E Structure Reports Online 68, no. 11 (2012): o3160. http://dx.doi.org/10.1107/s1600536812042997.

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Qin, Qi-Xue, Jian Yang, Duo-Zhi Chen, Bo Yang, and Ji Zhang. "An Alternate Preparation of 3,4,5-Trimethoxyphenol." Organic Preparations and Procedures International 45, no. 4 (2013): 321–24. http://dx.doi.org/10.1080/00304948.2013.798570.

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Muftah, Mohamed Saad. "Studies on Benzoxazine Derivaties." International Journal for Research in Applied Science and Engineering Technology 12, no. 5 (2024): 5589–90. http://dx.doi.org/10.22214/ijraset.2024.62844.

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Abstract: The 5, 6, 7 trimethoxy (1, 4) benzoxazine -2,3diones was synthesized by reaction of 2-amino-3,4,5 trimethoxyphenol with oxalyl chloride. The new compound of benzoxazine derivative was characterized by elemental analysis, mass spectroscopy , infrared and 1H-NMR . The compound exhibited antifungal and antibacterial activities.
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Liu, Xiuhua, Dongbao Zhao, and Hanqing Wang. "Phenolic compounds from Celastrus angulatus." Journal of Indian Chemical Society Vol.79, Mar 2002 (2002): 259–60. https://doi.org/10.5281/zenodo.5846201.

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Chemistry and Chemical Engineering College of Henan University, Kaifeng-475001, P.R. China <em>E-mail</em> : xiuhual@371.net <em>Fax</em> : 086-378-2852533 Lanzhou Institute of Chemical Physics, Chinese Academy of Science, Lanzhou-730000, P. R. China <em>Manuscript received 12 January 2001, revised 24 July 2001, accepted 6 August 2001</em> Four phenolic compounds (+)-catechin (1), (-)-epicatechin (2), 2,4,6-trimethoxyphenol-l<em>-&Omicron;</em>-&beta;-D-glucopyranoside (3), 3&beta;,7,3&#39;- trihydroxy- 4&#39;-methoxyflavan-l<em>-&Omicron;</em>-&beta;-D-glucopyranoside (4) together with dulcit
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Qin, Qi-xue, Jian Yang, Duo-zhi Chen, Bo Yang, and Ji Zhang. "ChemInform Abstract: An Alternate Preparation of 3,4,5-Trimethoxyphenol." ChemInform 45, no. 16 (2014): no. http://dx.doi.org/10.1002/chin.201416079.

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Faizi, Shaheen, Sadia Zikr-Ur-Rehman, and Muhammad Ali Versiani. "Shamiminol: A New Aromatic Glycoside from the Stem Bark of Bombax ceiba." Natural Product Communications 6, no. 12 (2011): 1934578X1100601. http://dx.doi.org/10.1177/1934578x1100601226.

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A new aromatic glycoside, shamiminol was isolated from the stem bark of Bombax ceiba along with the known constituents stigmasta-3,5-diene, lupenone, (±)-lyoniresinol 2a- O-β-D-glucopyranoside and opuntiol, obtained for the first time from this plant. The structure of shamiminol was elucidated on the basis of extensive 1D- and 2D-NMR spectroscopic and mass spectrometric studies as 3,4,5-trimethoxyphenol 1- O-β-D-xylopyranosyl-(1→2)-β-D-glucopyranoside (1).
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Thao, Nguyen Phuong. "PHENOLIC CONSTITUENTS FROM THE STEM BARKS OF RHIZOPHORA APICULATA BLUME." Vietnam Journal of Science and Technology 58, no. 5 (2020): 517. http://dx.doi.org/10.15625/2525-2518/58/5/14712.

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Using various chromatographic separations, seven phenolic derivatives (1‒7) were isolated from a methanolic extract of R. apiculata stem barks. Their structures were elucidated to be dunnianoside E (1), (+)-dihydroquercetin (2), 2,6-dimethoxy-[1,4]benzoquinone (3), 2,4,6-trimethoxyphenol (4), 3,4,5-trimethoxybenzyl alcohol (5), hydroxytyrosol (6), and methyl 3,4-dihydroxycinnamate (7) by detailed analysis via spectroscopic techniques (1D, 2D NMR and ESI-MS data) as well as comparison with those reported. This is the first report of compounds 1 and 4‒7 from Rhizophora genus.
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Feng, Shixiu, Jijiang Bai, Shengxiang Qiu(Samuel), Yong Li, and Tao Chen. "Iridoid and Phenolic Glycosides from the Roots of Prismatomeris connata." Natural Product Communications 7, no. 5 (2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700502.

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A new phenolic glycoside, 1- O-[β-D-glucopyranoyl-(1→6)-β-D-glucopyranosyl]-3,4,5-trimethoxyphenol, named prismaconnatoside (1), together with one known phenolic glycoside (2) and four aspruloside type iridoid glycosides (3-6) were isolated from the roots of Prismatomeris connata. Their structures were determined by spectroscopic and spectrometric methods. Based on the results, along with those from other studies, iridoids were suggested to be chemical markers to distinguish between P. connata and P. tetrandra, two species that are confused in traditional Chinese medicine.
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Matos, M. Agostinha R., Margarida S. Miranda, and Victor M. F. Morais. "3,4,5-Trimethoxyphenol: A combined experimental and theoretical thermochemical investigation of its antioxidant capacity." Journal of Chemical Thermodynamics 40, no. 4 (2008): 625–31. http://dx.doi.org/10.1016/j.jct.2007.11.006.

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Yake Nkom, Patience, Esther Offiong Asuquo, Lynius Ashipu Bebiaundeye, and Endurance Egwu Ukam. "GC-MS Evaluation of stem bark extract of sterculia oblonga for biomedical potentials." World Health Journal 5, no. 1 (2024): 16–21. http://dx.doi.org/10.47422/whj.v5i1.46.

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The stem-bark of sterculla oblonga, which is a rich lignocellulosic material, was analysed using GC-MS chromatography in other to identify the bioactive compounds present in the plant and deduce its possible therapeutic potentials. The pulverized plant sample was extracted by maceration for 48 hours using ethanol solvent, after solvent recovery, the crude extract was used for the GC-MS analysis. Results revealed the presence of 12 bioactive compounds namely: 1-(Butylsulfanyl)-2-ethoxyethane 4-methoxyphenol (mequinol), 2,6-dimethoxy-phenol (Syringol), 3,4,5-Trimethoxyphenol, 4,4,5,6-Tetramethyl
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Dissertations / Theses on the topic "Trimethoxyphenol"

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Slaghenaufi, Davide. "Contribution à la caractérisation des précurseurs d’arôme glycosylés du bois de chêne." Thesis, Bordeaux 2, 2012. http://www.theses.fr/2012BOR21987/document.

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La présence d’un métabolisme actif des bactéries lactiques dans le vin logé en fûts de chêne induit une augmentation de la concentration des composés volatils du bois. Ce phénomène a récemment été attribué à l'activité glycosidique des bactéries. Le glucoside précurseur d'un composé majeur de l’arôme boisé (whiskylactone) a déjà été identifié et quantifié dans le bois de chêne. Mais aucune donnée n'était disponible jusqu’à présent concernant l’identification formelle des précurseurs pour d’autres arômes du bois de chêne.Un premier travail a permis de montrer que les précurseurs monoglycosides
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Fourman, Cody. "Targeting oncogenic K-Ras and monoamine oxidase B utilizing chalcones bearing the 3,4,5-trimethoxyphenyl motif." Wright State University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1596823680746445.

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Popp, Friedrich. "(2,4,6-Trimethoxyphenyl)silane : Verwendung als geschützte Bausteine für die Synthese siliciumhaltiger Wirkstoffe sowie als Silylierungsreagenzien." kostenfrei, 2008. http://www.opus-bayern.de/uni-wuerzburg/volltexte/2008/2745/.

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Fischer, Markus [Verfasser], and Reinhold [Gutachter] Tacke. "Synthese neuartiger siliciumorganischer Wirkstoffe sowie siliciumhaltiger Synthese-Bausteine unter Verwendung der 4-Methoxyphenyl-, 2,6-Dimethoxyphenyl- und 2,4,6-Trimethoxyphenyl-Schutzgruppe / Markus Fischer. Gutachter: Reinhold Tacke." Würzburg : Universität Würzburg, 2015. http://d-nb.info/1112655638/34.

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Weisenberger, Verena [Verfasser]. "Casein Kinase 1 delta (CK1delta) und Kolorektale Karzinome: Nachweis von Mutationen in der Kinasedomäne von CK1delta sowie Validierung der Effekte von IC261 (3-[(2,4,6-trimethoxyphenyl)-methylidenyl]-indolin-2-one) in Kolontumorzelllinien / Verena Weisenberger." Ulm : Universität Ulm. Medizinische Fakultät, 2012. http://d-nb.info/1023728605/34.

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Tsai, Cheng-Yan, and 蔡承延. "Synthesis and Cytotoxic Activities of 1-(3,4,5-Trimethoxyphenyl)-1-(substituted)ethylene." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/38332158074699727448.

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碩士<br>中國文化大學<br>應用化學研究所<br>97<br>Combretastatin A-4 (CA-4), isolated from Combretum caffrum, strongly inhibited the polymerization of tubulin by binding to the colchicine site and showed strong cytotoxicity against a variety of human cancer cell lines. Phenstatin, a benzophenone compound related to CA-4, was synthesized by Pettit group, and showed strong cytotoxic activity against a variety of human cancer cell lines. In order to study the structure and cytotoxic activity relationship, we replaced the carbonyl group in phenstatin by ethylene or ethyl group to synthesize a series of phenstatin
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yuan, Chuang shun, and 莊舜淵. "Synthesis and Cytotoxic activity of 4-(indolyl)-5-(3,4,5-trimethoxyphenyl) isoxazole." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/26896720340144652012.

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碩士<br>中國文化大學<br>應用化學研究所<br>95<br>Combretastatin A-4 (CA-4), a natural product isolated from Combretum caffrum, strongly inhibited the polymerization of tubulin by binding to the colchicine site, and it showed strong cytotoxicity against a variety of human cancer cells. To date, many CA-4 analogues and their anticancer activity have been extensively studied. Its water-soluble derivative, sodium phosphate prodrug (CA-4P), is currently evaluated for clinical applications. The structure–activity relationship analysis of the combretastatins indicated that the cis configuration of the two aromat
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Popp, Friedrich. "(2,4,6-Trimethoxyphenyl)silane: Verwendung als geschützte Bausteine für die Synthese siliciumhaltiger Wirkstoffe sowie als Silylierungsreagenzien." Doctoral thesis, 2008. https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-27459.

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In Fortführung der bisher in dieser Forschungsgruppe durchgeführten Studien mit (2,4,6-Trimethoxyphenyl)silanen wurden im Rahmen der vorliegenden Arbeit weitere Untersuchungen zu den Schutzgruppen-Eigenschaften der Si-(2,4,6-Trimethoxyphenyl)-Gruppe angestellt und anschließend die hierbei gewonnenen Erkenntnisse verwendet, um Sila-Analoga bereits bekannter biologisch aktiver Verbindungen über neue Synthesewege mit (2,4,6-Trimethoxyphenyl)silanen darzustellen. Des Weiteren wurden im Rahmen der Untersuchungen zur C/Si-Bioisosterie die pharmakologischen Eigenschaften dieser bereits auf anderem We
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Popp, Friedrich [Verfasser]. "(2,4,6-Trimethoxyphenyl)silane : Verwendung als geschützte Bausteine für die Synthese siliciumhaltiger Wirkstoffe sowie als Silylierungsreagenzien / vorgelegt von Friedrich Popp." 2008. http://d-nb.info/991833678/34.

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Fischer, Markus. "Synthese neuartiger siliciumorganischer Wirkstoffe sowie siliciumhaltiger Synthese-Bausteine unter Verwendung der 4-Methoxyphenyl-, 2,6-Dimethoxyphenyl- und 2,4,6-Trimethoxyphenyl-Schutzgruppe." Doctoral thesis, 2015. https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-113987.

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Synthese siliciumhaltiger Wirkstoffe und Synthese-Bausteine des 4-Silapiperidin-Typs: Im Rahmen der systematischen Untersuchungen unseres Arbeitskreises zur C/Si-Bioisosterie wurde für bereits bekannte σ-Rezeptor-Antagonisten eine neue verbesserte Syntheseroute entwickelt, wobei die Endprodukte jeweils in einer sechsstufigen Synthese dargestellt und als entsprechende Hydrochloride isoliert wurden. Ein weiteres Teilprojekt der vorliegenden Arbeit betraf die Entwicklung einer Syntheseroute zur Darstellung von Sila-L-741,626, dem Sila-Analogon des selektiven D2-Dopamin-Rezeptorantagonisten L-741,
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Books on the topic "Trimethoxyphenol"

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DiFiore, Kenneth A. Synthetic routes to 4(2,3,4- Trimethoxyphenyl)-3-cyclohexen-1-one. 1988.

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Book chapters on the topic "Trimethoxyphenol"

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Aggarwal, P., and M. W. P. Bebbington. "Cyclization of 5-[Hydrazono(3,4,5-trimethoxyphenyl)methyl]-1,2,4-triazin-6(1)-ones." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-117-00253.

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Conference papers on the topic "Trimethoxyphenol"

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McCarthy, Florence, Kevin O'Shea, Michael Cahill, and Larry Pierce. "Synthesis and anticancer activity of novel indole-trimethoxyphenyl conjugates." In 4th International Electronic Conference on Medicinal Chemistry. MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05640.

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Gagné-Boulet, Mathieu, Sébastien Fortin, Jacques Lacroix, Carole-Anne Lefebvre, Marie-France Côté, and René C-Gaudreault. "Abstract 1664: New moieties mimicking the trimethoxyphenyl (ring A) of combretastatin A-4: Synthesis and biological evaluation." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-1664.

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Prabhu, A. N., V. Upadhyaya, A. Jayarama, et al. "Synthesis, Growth And Characterization of 1-(5-chlorothiophen-2-yl)-3-(2,4,5-Trimethoxyphenyl) Prop-2-en-1-one Single Crystal: A Potential NLO Material." In OPTICS: PHENOMENA, MATERIALS, DEVICES, AND CHARACTERIZATION: OPTICS 2011: International Conference on Light. AIP, 2011. http://dx.doi.org/10.1063/1.3643603.

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Effendy, A. H. White, Abarrul Ikram, et al. "Synthesis and X-ray Structural Study on the Complexes of Silver(I) Halide with Tricyclohexylephosphine, Diphenyl-(2,4,6-trimethoxy)phenylphosphine, Phenyl-2,4,6-trimethoxyphenyl phosphine, and Tris(2,4,6-trimethoxy)phenylphosphine." In NEUTRON AND X-RAY SCATTERING 2007: The International Conference. AIP, 2008. http://dx.doi.org/10.1063/1.2906094.

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Yudhani, Ratih Dewi, Dwi Aris Agung Nugrahaningsih, Eti Nurwening Sholikhah, and Mustofa Mustofa. "The 1,4-bis(3,4,5-trimethoxyphenyl)-tetrahydro-furo(3,4-c) furan isolated from Swietenia macrophylla King. improves the morphology of liver skeletal muscles cells as insulin resistance model induced by palmitate acid." In THE 4TH INTERNATIONAL CONFERENCE ON LIFE SCIENCE AND TECHNOLOGY (ICoLiST). AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0111536.

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Journal articles
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