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Relevant bibliographies by topics / 4-methoxyphenyl

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Academic literature on the topic '4-methoxyphenyl'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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Journal articles on the topic "4-methoxyphenyl"

1

Brown, RFC, WR Jackson, TD Mccarthy, and GD Fallon. "Reactions of Methyl threo-2-Acetoxy-3-chloro-3-(4-methoxyphenyl)propanoate and Methyl cis-2,3-Epoxy-3-(4-methoxyphenyl)propanoate With 3,5-Dimethoxyphenol: Potential Routes to Flavan-3-ols." Australian Journal of Chemistry 45, no. 11 (1992): 1833. http://dx.doi.org/10.1071/ch9921833.

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Attempted syntheses of flavan-3-ols by reaction of either methyl threo-2-acetoxy-3-chloro-3-(4-methoxypheny1)propanoate (3) or methyl cis-2,3-epoxy-3-(4-methoxypheny1)propanoate (14) with 3,5-dimethoxyphenol failed to give the required aryl ethers. Products usually were derived from C-alkylation of the electron-rich phenol although reaction of the chloro acetate (3) with the phenoxide ion gave the furanone (5). The single-crystal X-ray structures of methyl 4-hydroxy-3-(4-methoxyphenyl)-2-(4-methoxyphenylmethyl)-5-oxo-2,5-dihydrofuran-2-carboxylate and cis-3-hydroxy-5,7-dimethoxy-4(4-methoxyphenyl)-3,4dihydr-2H-1-benzopyran-2-one have been determined.

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Gowda, B. Thimme, Sabine Foro, Roopa Nayak, and Hartmut Fuess. "4-Methoxyphenyl benzoate." Acta Crystallographica Section E Structure Reports Online 63, no. 8 (July 18, 2007): o3507. http://dx.doi.org/10.1107/s160053680703406x.

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Flower, Kevin R., Philip J. Miles, and Robin G. Pritchard. "(4-Methoxyphenyl)diphenylphosphine." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (February 16, 2007): o1339—o1340. http://dx.doi.org/10.1107/s1600536807007271.

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Akkurt, Mehmet, Irfana Mariam, Ifrah Naseer, Islam Ullah Khan, and Shahzad Sharif. "N-(4-Methoxyphenyl)-4-methylbenzenesulfonamide." Acta Crystallographica Section E Structure Reports Online 67, no. 1 (December 18, 2010): o186. http://dx.doi.org/10.1107/s1600536810052633.

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Haase, W., H. Paulus, G. Strobl, and W. Hotz. "Mesogenic 4-methoxyphenyl 4-hexyloxybenzoate." Acta Crystallographica Section C Crystal Structure Communications 47, no. 9 (September 15, 1991): 2005–6. http://dx.doi.org/10.1107/s0108270191002731.

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6

Liu, Wei, and Lida Tang. "(4-Methoxyphenyl)(4-methylcyclohexyl)methanone." Acta Crystallographica Section E Structure Reports Online 68, no. 10 (September 5, 2012): o2850. http://dx.doi.org/10.1107/s1600536812037373.

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Ding, Chun-Lei, Yong-Jie Wu, Yi Zhang, and Li Zhou. "(4-Ethylcyclohexyl)(4-methoxyphenyl)methanone." Acta Crystallographica Section E Structure Reports Online 69, no. 3 (February 6, 2013): o348. http://dx.doi.org/10.1107/s1600536813003279.

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Wang, Ling, Zi-Qian Chang, Jie Zhang, and Cheng-Min Li. "(4-Methoxyphenyl)(4-propylcyclohexyl)methanone." Acta Crystallographica Section E Structure Reports Online 69, no. 3 (February 20, 2013): o404. http://dx.doi.org/10.1107/s1600536813003644.

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Zhang, Xiao-Meng, Cang Zhang, Wen-Ping Zhang, and Xiao-Rong Liu. "4-(3-Fluoro-4-methoxyphenyl)-1-(4-methoxyphenyl)-5-(3,4,5-trimethoxyphenyl)-1H-imidazole." Acta Crystallographica Section E Structure Reports Online 66, no. 12 (November 6, 2010): o3084. http://dx.doi.org/10.1107/s160053681004465x.

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Collins, DJ, and HA Jacobs. "Steric and Stereoelectronic Effects in the Hydrogenolysis and Birch Reduction of Some Hindered Tertiary-Benzylic Carbinols." Australian Journal of Chemistry 40, no. 12 (1987): 1989. http://dx.doi.org/10.1071/ch9871989.

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3-(4'-Methoxyphenyllpentan-3-ol (3a) and 3-(4'-methoxypheny1)-2,4-dimethylpentan-3-ol (3b) underwent catalytic hydrogenolysis over 10% palladium/charcoal at moderate temperatures and pressures. The more hindered tertiary-benzylic carbinols 3-(4'-methoxypheny1)-2,2,4-trimethylpentan-3-ol (6), 3-(4'-methoxyphenyl)-2,2,4,4-tetramethylpentan-3-ol (3c), 1-(4'- methoxyphenyl )-2,2,6,6-tetramethylcyclohexan-l-ol (8) and 1-(1',1'-dimethylethy1)-6-methoxy- 2,2-dimethyl-l,2,3,4-tetrahydronaphthalen-1-ol (10) were completely resistant to hydrogenolysis, even under vigorous conditions. While the hindered tertiary-benzylic carbinols (6),(8) and (10) readily underwent Birch reduction, the analogous di-t-butyl anisyl carbinol (3c) was unchanged. The failure of (3c) to undergo Birch reduction is probably due to a hitherto unrecognized stereoelectronic effect: the C-OH bond of (3c) is constrained to lie more or less in the plane of the benzene ring, and addition of an electron to the benzene ring of the derived oxyanion (31) is inhibited in this conformation.

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Dissertations / Theses on the topic "4-methoxyphenyl"

1

Ying, Hu. "Synthesis and Photophysical Properties of 3D Substituted Heterohelicenes and their Derivatives." Bowling Green State University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1224602780.

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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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Chan, Yi-Cheng, and 詹沂澄. "Synthesis and biological evalution of 7-(4-Methoxyphenyl)tetrahydroquinazolinone derivatives." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/59666684186884373450.

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碩士
中國醫藥大學
藥物化學研究所碩士班
99
Inflammation is the protective response of the injury or microbialinvasion. Overexpression of the inflammatory response and continuous inflammation is closely related to many diseases.Cytokines, adhesion molecules,growth factors and inflammatory factors,and so a large number of enzymes expressed in many inflammatory reactions and the formation of inflammation-related diseases.Inflammatory hormone agonist is a role of inflammatory drug targets for inflammation and symptoms in addition to steroid drugs alsoNSAIDs. Shown in the literature of compounds with naphthyridinones moieties have a variety of pharmacological activities, including anti- inflammatory,and antimicrotubule polymerization. On the other hand amino-quinazolinone in cancer research have been found to inhibit Heat shock protein 90(HSP 90), Lck kinase and other effects, such derivatives have shown potential anticancer activity. To find the path through inhibition of Lck kinase, we also find the relevant aminopyrimidine and its derivativeshave the effect of blocking the MAPK pathway and also has antiinflammatory potential. We try to use the characteristics of these three compounds,synthesis of phenyldihydroquinazolinone the main frame of the compounds.For cell linessuch as A549,PC3,AGS,TW01, compounds can inhibit the activity of cell line proliferation.

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Lu, Chia-Hao, and 呂家豪. "Synthesis and anticancer activity of 6-(4-methoxyphenyl) tetrahydroindazolone derivatives." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/24669673103122547647.

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碩士
中國醫藥大學
藥物化學研究所碩士班
99
6-(Methoxyphenyl)tetrahydroindazol-4-one derivatives were synthesized and evaluated for antiproliferative activity. Structure-activity relationship was elucidated with various substitutions on the N-1 aryl moiety of tetrahydroindazol-4-one. A novel N-2 aryl-substituted skeleton was established by microwave synthesis. The bioevaluative result was shown that the N-1 substituted tetrahysroindazol-4-one possessed more potential activity against human lung cancer cell (H226), leukemia (Jurkat cell), and nasopharyngeal carcinoma cell (NPC-TW01) than those of corresponding N-2 derivatives. The introduction of oxime moiety at 4-position of tetrahydroindazoles led to a loss of the cytotoxic activity.

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Huang, Cong-Long, and 黃聰龍. "Synthesisandβ-adrenoceptorblockingeffectsofDZBN(4-[4'-(2-hydroxy-3-tert-butylaminopropoxy)-3'-methoxyphenyl]-3-buten-2-one)." Thesis, 1993. http://ndltd.ncl.edu.tw/handle/25685030766414200978.

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Wu, Bo-Jian, and 吳柏樫. "Pyrolytic Study of 2-Azidocycloheptanone and 2-[2-(4-Methoxyphenyl)vinyl]benzofuran." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/44309324906805227381.

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碩士
國立中山大學
化學系研究所
93
Flash vacuum pyrolysis (FVP) of 2-azidocycloheptanone gave two products: 3,4,5,6-tetrahydro-1H-azocin-2-one and 1-hydroxy-2-oxo-4- azabicyclo[5.3.0]dec-4-ene-3-spiro-2’-cycloheptanone. Flash vacuum pyrolysis of 2-[2-(4-methoxyphenyl)vinyl]benzofuran gave two products: 4-(2-benzofuran-2-ylvinyl)phenol and 1H-6-oxacyclopenta[c]fluorine.

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Chuan-YiWu and 吳傳益. "Synthesis and Discussion of 6-Methoxy-1, 2, 3, 4-Tetraphenylnaphthalene and 1-(4-Methoxyphenyl)-2, 3, 4-Triphenylnaphthalene." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/25673322724513373472.

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8

Chen, Rong-Yu, and 陳溶諭. "Synthesis and Bioevaluation of 6-(4-Methoxyphenyl)-2-aminobenzofuran Derivatives as Enolase Inhibitors." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/pswtn2.

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碩士
中國醫藥大學
藥物化學研究所碩士班
102
Cancer is the leading cause of death in worldwide, and the process of metastasis formation leads to the majority of deaths associated with cancer. Alpha-enolase (ENO-1) has a significant role in cancer metastasis, and ENO-1 linked with glycolysis and energy metabolism in both normal and cancer cells. Therefore, we hoped that inhibited ENO-1 expression could decrease cell migration and invasion. A series of 2-aminobenzofuran derivatives has been successfully synthesized previously and subject to bioevaluation for ENO-1 activity in vitro. That result was shown that the compound BL-082 could inhibit 75% activity of ENO-1 at the value of 10 μM and had cytotoxicity for high metastatic lung adenocarcinoma cells (CL1-5). The thesis was following the previous result to deeply investigate the structure-activity relationship of 2-aminobenzofuran at the substitution of NH2 moiety for ENO-1 activity. The results were shown that the substitution of withdrawing group or donating group on 2-aminobenzofuran could attenuate the ENO-1 inhibitive activity. The compound 11p possessed 2-furonyl substitution on 2-amino moiety was illustrated the good inhibitive activity for ENO-1.

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Liu, Chin-Yu, and 劉晉育. "Synthesis of hydrophilic derivatives of 5-Methyl-2-(3-methoxyphenyl)-1,8-naphthyridin-4-one." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/03648744475882260917.

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碩士
中國醫藥大學
藥物化學研究所碩士班
94
In our previous studies of 2-phenyl-1,8-naphthyridine-4-one (2-PN) derivatives, compounds with a methyl group at the 5- or 6- position, were potent inhibitors of tubulin polymerization and showed remarkable cytoxicity in vitro against leukemia (HL-60), prostate cancer (PC-3), ovarian cancer (OVCAR-3), CNS cancer (SF-295) and melanoma (SF-MEL-5). 2-phenyl-1,8-naphthyridine-4-ones were synthesized according to following steps: condensation of substituted 2-aminopyridines (4,5) with substituted ethyl benzoylacetates (3) in the presence of polyphosphoric acid formed the corresponding pyridopyrimidinones (6,7). These kinetically favored products were then thermally converted at 350℃ in liquid paraffin to 2-PN (8,9). However, the low water-solubility of 2-PN limits its efficacy in vivo. In order to improve bioavailability by increasing solubility, we introduced hydrophilic group into the 4-position of 2-PN to form 5-methyl-2-(3-methoxyphenyl)-4-O-(β-D-glucopyranosyl)-1,8-naphthyridine (12) and substituted 2-phenyl-1,8-naphthyridin-4-oxyalkylcarboxylic acid (17-24) as target compounds. Further pharmacokinetic investigation is underway to determine if hydrophilic substitution of the 4-position of 2-PNs will result in compounds with increased bioavailability.

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Hwang, Tsong-Long, and 黃聰龍. "Synethesis and .beta.-adrenoceptor Blocking Effects of DZBN(4- [4'-(2-hydroxy-3-tert-butylaminopropoxy)-3'-methoxyphenyl]- 3buten-2-one)." Thesis, 1993. http://ndltd.ncl.edu.tw/handle/81033176603565273697.

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Book chapters on the topic "4-methoxyphenyl"

1

Winkelmann, Jochen. "Self-diffusion coefficient of 4-butyl-N-[(4-methoxyphenyl)methylene]- benzenamine." In Diffusion in Gases, Liquids and Electrolytes, 424. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_255.

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Winkelmann, Jochen. "Diffusion coefficient of 4-hydroxy-3-methoxyphenyl-acetic acid in water." In Diffusion in Gases, Liquids and Electrolytes, 890. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_667.

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Winkelmann, Jochen. "Diffusion coefficient of (4-hydroxy-3-methoxyphenyl)-glycolic acid in water." In Diffusion in Gases, Liquids and Electrolytes, 891. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_668.

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Winkelmann, Jochen. "Diffusion coefficient of 7-hydroxy-3-(4-methoxyphenyl)-8-methyl-4H-1-benzopyran-4-one in methanol." In Diffusion in Gases, Liquids and Electrolytes, 1114. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_890.

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Winkelmann, Jochen. "Diffusion coefficient of 7-hydroxy-3-(4-methoxyphenyl)-8-methyl-4H-1-benzopyran-4-one in acetonitrile." In Diffusion in Gases, Liquids and Electrolytes, 1115. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_891.

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Winkelmann, Jochen. "Diffusion coefficient of 7-hydroxy-3-(4-methoxyphenyl)-8-methyl-4H-1-benzopyran-4-one in ethanol." In Diffusion in Gases, Liquids and Electrolytes, 1116. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_892.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex derived from 1,2-di(4-methoxyphenyl-tellurato)-o-xylene." In Magnetic Properties of Paramagnetic Compounds, 312–13. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_163.

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Winkelmann, Jochen. "Diffusion coefficient of 7-hydroxy-3-(4-methoxyphenyl)-8-methyl-4H-1-benzopyran-4-one in propan-2-ol." In Diffusion in Gases, Liquids and Electrolytes, 1117. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_893.

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Alvarez, Marion, and Didier Le Bars. "Synthesis of 4-(2′-Methoxyphenyl)-1-[2′-(N-2″Pyridinyl)-p-[18F]Fluorobenzamido]Ethylpiperazine [18F]MPPF." In Radiochemical Syntheses, 87–94. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118140345.ch10.

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Shao, Xia, Keunsam Jang, and Peter J. H. Scott. "Synthesis of 1-(2,4-Dichlorophenyl)-4-Cyano-5-(4-[11C]methoxyphenyl)-N-(Piperidin-1-yl)-1H-Pyrazole-3-Carboxamide ([11C]OMAR)." In Radiochemical Syntheses, 73–80. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118834114.ch8.

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Conference papers on the topic "4-methoxyphenyl"

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Bulavka, Vladimir, Alexander Shchavlinskii, and Oleg Tolkachev. "N-Methyltyramine and N,O-Dimethyltyramine Synthesis via Intermediate 4-Methoxyphenyl-N-methyltioacetamide." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01731.

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Kovalev, Igor S., Dmitry S. Kopchuk, Olga S. Taniya, Nataliya V. Slovesnova, Alexey P. Krinochkin, Grigory V. Zyryanov, Vladimir L. Rusinov, and Oleg N. Chupakhin. "Synthesis of 5-(4-methoxyphenyl)-2,2′-bipyridine-based Schiff base with pyrene moiety." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0019983.

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Zhao, Bingbing, Yuping Guo, Zhou Lan, and Shan Xu. "Synthesis of tert-butyl 5-amino-4 - ((2- (dimethylamino) ethyl) (methyl) amino) -2- methoxyphenyl) Carbamate." In 2016 7th International Conference on Education, Management, Computer and Medicine (EMCM 2016). Paris, France: Atlantis Press, 2017. http://dx.doi.org/10.2991/emcm-16.2017.41.

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Sandhya, H. J. Ravindra, Praveen B. Managutti, and Tayur N. Guru Row. "Synthesis, crystal growth and characterization of (1E, 4E)-1, 5-bis (4-methoxyphenyl) penta-1, 4-dien-3-one (BMPD)." In PROCEEDINGS OF THE INTERNATIONAL CONFERENCE ON PHYSICS OF MATERIALS AND NANOTECHNOLOGY ICPN 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0009161.

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Chen, Xiao-Bing, Jun Xu, Po Zhao, Zun-Hua Yang, and Hong Peng. "Lipid lowering activity of (E)-3-[4-[2-(4-chlorophenoxy)-2-methylpropanoylox y]-3-methoxyphenyl] acrylic acid (AZ) in hyperlipidemic rats." In 2011 International Conference on Remote Sensing, Environment and Transportation Engineering (RSETE). IEEE, 2011. http://dx.doi.org/10.1109/rsete.2011.5966150.

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Duan, Fang, and Gang Liu. "Synthesis and properties of 1-[2-methyl-5-(4-methoxyphenyl)-3-thienyl]-2-[2-methyl-5-(4-chlorphenyl)-3-thienyl] perfluorocyclopentene." In 2015 International Workshop on Materials, Manufacturing Technology, Electronics and Information Science. WORLD SCIENTIFIC, 2016. http://dx.doi.org/10.1142/9789813109384_0008.

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Öner, Nazmiye, Ömer Tamer, Davut Avci, and Yusuf Atalay. "A theoretical study on 3-(4-methoxyphenyl)-1-(pyridin-2-Yl) prop-2-en-1-one." In 9TH INTERNATIONAL PHYSICS CONFERENCE OF THE BALKAN PHYSICAL UNION (BPU-9). AIP Publishing LLC, 2016. http://dx.doi.org/10.1063/1.4944226.

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Arianingrum, Retno, and Indyah Sulistyo Arty. "The effect of bromo chalcone [1-(4’-bromophenyl)-3-(4-hydroxy-3-methoxyphenyl)-2-propene-1-on] on T47D breast cancer cells." In 2ND INTERNATIONAL CONFERENCE ON CHEMISTRY, CHEMICAL PROCESS AND ENGINEERING (IC3PE). Author(s), 2018. http://dx.doi.org/10.1063/1.5065031.

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Ravindrachary, V., Vincent Crasta, R. F. Bhajantri, and J. Indira. "Optical, dielectric and micro hardness studies on 1-(4-methylphenyl)-3-(4-methoxyphenyl)-2-propen-1-one: a nonlinear optical single crystal." In Optics & Photonics 2005, edited by Manfred Eich. SPIE, 2005. http://dx.doi.org/10.1117/12.616642.

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Alande, Balaji D., C. G. Renuka, G. N. Sushma, M. Suma, Basavaraj Sannakki, and Y. F. Nadaf. "Quantum chemical studies on structure and electronic properties of the 2,7-bis(4-methoxyphenyl) 9,9-dipropyl-9H-flurene." In PROF. DINESH VARSHNEY MEMORIAL NATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF MATERIALS: NCPCM 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5098664.

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Reports on the topic "4-methoxyphenyl"

1

Mudge, Christopher, Bradley Sartain, Benjamin Sperry, and Kurt Getsinger. Efficacy of florpyrauxifen-benzyl for eurasian watermilfoil control and nontarget Illinois pondweed, elodea, and coontail response. Engineer Research and Development Center (U.S.), September 2021. http://dx.doi.org/10.21079/11681/42063.

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This research evaluated low concentrations and short exposure times of the recently registered aquatic herbicide florpyrauxifen-benzyl (4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoro-pyridine-2-benzyl ester) on the target plant Eurasian watermilfoil (Myriophyllum spicatum L., hereafter referred to as EWM) as well as selectivity towards the nontarget submersed species Illinois pondweed (Potamogeton illinoensis Morong), elodea (Elodea canadensis Michx.), and coontail (Ceratophyllum demersum L.)

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