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Dissertations / Theses on the topic 'Methoxypheny'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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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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2

Harrison, Karl Nicholas. "The synthesis and characterisation of Tris(2-methoxyphenyl)phosphite nickel palladium and platinum complexes." Thesis, University of Bristol, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303757.

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3

Axelsson, Karolin. "Chemical signals in interactions between Hylobius abietis and associated bacteria." Doctoral thesis, KTH, Organisk kemi, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-187817.

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The pine weevil (Hylobius abietis L.) is one of the two topmost economically important insect pests in Swedish conifer forests. The damage increase in areas were the silvicultural practice is to use clear cuttings were the insects gather and breed. During egglaying the female protects her offspring by creating a cave in roots and stumps were she puts her egg and covers it with frass, a mixture of weevil feces and chewed bark. Adult pine weevils have been observed to feed on the other side of the egg laying site and antifeedant substance has been discovered in the feces of the pine weevil. We t

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4

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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5

Soodin, Mahamed Ally. "The attempted synthesis of 2'-[2-amino-3(p-methoxyphenyl) propanamiodo]-2'-deoxy-N'6N'6-dimethyladenosine, an isomer of the antibiotic and antitumour drug puromycin." Thesis, City University London, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387375.

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6

Roose, Max. "Photolibération de monoxyde d'azote dans des complexes de ruthénium nitrosyle à ligands polypyridines fonctionnalisés par des groupes fluorène ou méthoxyphényle." Thesis, Toulouse 3, 2018. http://www.theses.fr/2018TOU30189/document.

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Le monoxyde d'azote (NO•) est connu pour son rôle dans de nombreux processus biologiques et physiologiques. Il peut cependant avoir des effets antagonistes selon sa concentration dans le milieu. Le développement de sources exogènes capables de relarguer localement et quantitativement NO• est donc nécessaire pour profiter pleinement de son potentiel thérapeutique. La chimiothérapie photoactivée offre une approche intéressante qui consiste en l'irradiation de systèmes photosensibles non toxiques dans l'obscurité, mais capables de déclencher la mort cellulaire sous activation à la lumière. Cette

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7

Ricquebourg, Emilie. "Etude de la réactivité et de la toxicité des particules de méthoxyphénols : analyse de leur action in vivo chez le rat en atmosphère contrôlée sur la fonction cardiaque et les paramètres du stress oxydant." Thesis, Aix-Marseille, 2014. http://www.theses.fr/2014AIXM4711.

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De manière générale, l'inhalation de particules entraîne des réactions inflammatoires et des réactions d'oxydo-réduction responsables de la dégradation des matrices biologiques qui exercent, de plus, un fort impact cardio-vasculaire. La combustion du bois est une source majeure de composés organiques semi-volatils, parmi lesquels les méthoxyphénols (MPs), tels que le coniféryl aldéhyde (CA), le syringaldéhyde (SR), ou l'acétosyringone (AS). Les MPs sont néanmoins peu étudiés dans la littérature alors que la toxicité d'autres composés également issus de la combustion de la biomasse, tels que le

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8

Ricquebourg, Emilie. "Etude de la réactivité et de la toxicité des particules de méthoxyphénols : analyse de leur action in vivo chez le rat en atmosphère contrôlée sur la fonction cardiaque et les paramètres du stress oxydant." Electronic Thesis or Diss., Aix-Marseille, 2014. http://www.theses.fr/2014AIXM4711.

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De manière générale, l'inhalation de particules entraîne des réactions inflammatoires et des réactions d'oxydo-réduction responsables de la dégradation des matrices biologiques qui exercent, de plus, un fort impact cardio-vasculaire. La combustion du bois est une source majeure de composés organiques semi-volatils, parmi lesquels les méthoxyphénols (MPs), tels que le coniféryl aldéhyde (CA), le syringaldéhyde (SR), ou l'acétosyringone (AS). Les MPs sont néanmoins peu étudiés dans la littérature alors que la toxicité d'autres composés également issus de la combustion de la biomasse, tels que le

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9

Lie, Wu Fu, and 吳福利. "Solid-Liquid Equilibria for Catehol/4-Methoxyphenol." Thesis, 1996. http://ndltd.ncl.edu.tw/handle/80439110064751809735.

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碩士<br>國立臺灣科技大學<br>化學工程研究所<br>84<br>1,4-Butanediol is used as an auxiliary agent in the present study to separate the close-boiling, eutectic mixture of 4-methoxyphenol and catechol by a crystallization method. Solid- liquid equilibria (SLE) were measured by a solid-disappearance method for the binary and the ternary systems composed of 4- methoxyphenol, catechol, 1,4-butanediol, or p-cresol. The results show that a 1:1 adducted compound forms in the 1,4-butanediol+catechol mixtures. A sepa

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10

Chiu, I.-Chen, and 邱一真. "Synthesis of 4-Bromotropolone from 2-Methoxyphenol." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/20043790713531274753.

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碩士<br>中原大學<br>化學研究所<br>99<br>This research uses 2-methoxyphenol to synthesize 3-bromines and 4- bromines MOB 66 and 72. Responded separately with the Corey-Chaykovsky reagent to act cyclopropane alkylation respond, to obtains including the bromine’s Shuanghuan [4.1.0] heptenone skeletons 67 and 73. This response, may possibly influence by the bromine substituting steric hindrance and the electronic effect to occured in the different duplet bond (respectively is C2=C3, with C4=C5) on the cyclopropane alkylation. Once again the compound 67 and 73 using the acid hydrolysis to get the same diketon

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11

chang, Yu-pei, and 張毓珮. "Synthesis of 4-Aryltropolones from 2-methoxyphenol." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/89238430569559683217.

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碩士<br>中原大學<br>化學研究所<br>99<br>In this study, at first we used bromination to introduct a bromine on the 4-position of 2-methoxy phenol. Then used employed palladium-catalyzed cross-coupling Suzuki Coupling to get various aromatic compounds, which were oxidized to the correspounding 4–aryl masked o-benzoquinone, Corey-Chaykovsky reagent (CCR) 1 eq. was used for cyclopropanation reaction of MOBs to construct bicyclo[4.1.0]heptenone systems. Which were then converted to 4-aryl tropolones via hydrolysis of the ketal group, ring expansion by boron trifluoride-ether, and hydrolysis the difluoro borat

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12

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<br>中國醫藥大學<br>藥物化學研究所碩士班<br>99<br>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 naph

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13

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<br>中國醫藥大學<br>藥物化學研究所碩士班<br>99<br>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 corre

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14

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<br>國立中山大學<br>化學系研究所<br>93<br>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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15

Tseng, Shu Li, and 曾淑麗. "Separation of 4-methoxyphenol + catechol mixtures by distillative freezing process." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/58640714701454169717.

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碩士<br>長庚大學<br>化工與材料工程研究所<br>96<br>A new separation technique, called distillative freezing (DF), is introduced in this work to separate the mixture of 4-methoxyphenol and catechol. In principle, the DF process is operated at a triple-point condition in which the liquid mixture is simultaneously vaporized and solidified due to the three-phase equilibrium. It results in the formation of pure solid and both liquid and vapor phase of mixtures. In essence, the process is continued until the liquid phase is completely eliminated and only the pure solid crystals remain in the feed. The experimental r

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16

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<br>中國醫藥大學<br>藥物化學研究所碩士班<br>102<br>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

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17

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<br>中國醫藥大學<br>藥物化學研究所碩士班<br>94<br>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 aci

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18

Liao, Ping-Heng, and 廖秉恆. "Kinetics Study of Methoxybenzoylation of p-Methoxyphenol over Phase-Transfer Catalysts." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/52098136865789483301.

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碩士<br>國立中興大學<br>化學工程學系<br>90<br>e of phase-transfer catalysts,volume ratio of aqueous and solvent, and so on. From the experimental data shown, the substitution reaction was greatly enhanced by applying phase-transfer catalysis. Without the addition of any catalyst, the product yield is very low, while the reaction rate increases with increasing the amounts of TBAB catalyst added ,and the overall reaction rate can be well described by the pseudo-first-order kinetics. And using TBPB as the ,the product yield was obtained above 95% under very mild conditions. An optimal quantity of NaOH is loca

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19

Huang, Cong-Long, та 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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20

HUANG, CIANG-YU, and 黃薔瑜. "Synthesis and electrochromic characterization of triazole, thiazole, benzothiazole, and methoxyphenoxy-containing polydithienylpyrroles." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/6gf7ye.

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碩士<br>國立雲林科技大學<br>化學工程與材料工程系<br>106<br>In this study, triazole, benzothiazole, methylthiazole, and methoxyphenoxy groups are incorporated to dithienylpyrroles using Paal-Knorr reaction, which are denominated as TN, BT, MP, and MT, respectively. Their corresponding polydithienylpyrroles (PTN, PBT, PMP, and PMT) are synthesized using electrochemical polymerization and are employed as the anodic coloring materials of electrochromic devices (ECDs). Moreover, a cathodic coloring material (POTP) is also synthesized electrochemically. PMP film is goldenrod in the neutral state, it turns into dark gol

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21

Lin, Chao-Jung, and 林昭蓉. "Synthesis of Carbamate and Amine derivatives of(5 or 6)-Methyl-2-(3-methoxyphenyl)-1,8-naphthyridine." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/47037739675343332384.

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碩士<br>中國醫藥大學<br>藥物化學研究所碩士班<br>94<br>5-Methyl-2-(3-methoxyphenyl)-1,8-naphthyridine (6a) and 6-methyl-2-(3-methoxyphenyl)-1,8-naphthyridine (6b) have been synthesized and shown potent cytotoxicity. However, during the undergoing in vivo tests and other preclinical studies, their limited water solubility complicated the issues of IV preparation and oral formulation. To simplify these issues several carbamate and amine derivatives of 6a were synthesized and their cytotoxicity were examined. Strangely, attempted to introduce a bromo group into the benzylic carbon of 6a or 6b by treatment with NBS

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賴玉琪. "Synthesis and biological activities of (2E)-3-[2-(substituted benzyloxy0-4(or 5) methoxyphenyl] acrylaldehyde derivatives." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/01580863496631727352.

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23

Liao, Ying-Chi, and 廖英錡. "Pyrolytic Study of 2-(2-Vinylstyryl)furan derivatives and 2-[2-(4-Methoxyphenyl)vinyl]benzo[b]thiophene." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/32400694735627980679.

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碩士<br>國立中山大學<br>化學系研究所<br>94<br>Flash vacuum pyrolysis of 2-(2-vinylstyryl)furan derivatives via electrocyclization followed by dehydrogenation will give 2-(2-naphthalen-2-yl)furan analogues, on the other hand, FVP of 2-(2-vinylstyryl)furan derivatives via electrocyclization followed by [1,5]-H shift will give 3-(2-furyl)-1,2-dihydronaphthalene analogues. FVP of 2-[2-(4-methoxyphenyl)vinyl]benzo[b]thiophene gave three products: trans-4-(2-benzo[b]thiophen-2-ylvinyl)phenol, benzo[b]naphtha[1,2-d]thiophen-2-ol and 1H-6-thiacyclopenta[c]fluorene.

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Chou, Chih-Tsung, and 周志聰. "Pyrolytic and Photolytic Studies of 3- (o-Methoxyphenyl)-1-phenylprop-2-en-1-one and Its Derivatives." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/46785235206508055709.

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碩士<br>國立中山大學<br>化學系研究所<br>98<br>Pyrolysis of 3- (o-methoxyphenyl)-1-phenylprop-2-en-1-one(49) 、1- (o-methoxyphenyl)-3-phenylprop-2-en-1-one (50) and 1-(o-methoxyphenyl)-3-phenylprop -2-yn-1-one (51) gave the expected cyclic products 2-phenylbenzo[b]furan (11) and flavone (73). Furthermore, compounds 49-51 gave phenanthrene-9,10-dione (71)、fluoren-9-one (14) and others as the minor products at high temperture. Under photolytic condition, compounds 49-51 gave photocyclic product (73) all in low yields and recovered mostly the starting materials.

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25

蘇長清. "Vapor-Liquid Equilibria for Binary Mixtures of 2-Methoxyphenol, 1,2-Dimethoxybenzene and Auxiliary Agents." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/13471579965990746107.

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碩士<br>國立臺灣科技大學<br>化學工程系<br>90<br>A static-type apparatus with a liquid-phase circulation loop was used to measure isothermal vapor-liquid equilibrium ( VLE ) data for the systems containing high-melting point compounds. The apparatus was also employed to determine vapor pressures for 2-methoxyphenol, 1,2-dimethoxy -benzene, morpholine, tert-butanol, 2-butoxyethyl acetate, 2-2(ethoxyethoxy)ethyl acetate, diethyl methylmalonate, diethylene glycol diethyl ether, diethylene glycol dibutyl ether, and diethylene glycol hexyl ether at temperatures from 308.15 K to 473.15 K and pressures from 2 kPa

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Weng, Zi-Wen, and 翁子文. "Solid-Liquid Equilibria for Separating Closely Boiling Mixtures of 2-Methoxyphenol and 1,2-Dimethoxybenzene." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/22767821182806350574.

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碩士<br>國立臺灣科技大學<br>化學工程系<br>90<br>The objective of this study is to investigate the solid-liquid equilibrium (SLE) behavior for the mixtures, which are related to the separation of closely boiling mixtures of 2-methoxyphenol and 1,2-dimethoxybenzene via extractive or adductive crystallization method. tert-Butanol or morpholine was served as an auxiliary agent. The SLE data were measured with solid-disappearance method for various binary and ternary mixtures. The results showed that a 2:1 adducted compound formed in the system of tert-butanol + 2-methoxyphenol, and 1:4 and 1:1 adducted compou

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Wu, Hsien-Ming, and 吳憲銘. "Cardiovascular pharmacology of GPFER:3-[4'-(2-hydroxy- 3-tert- butylaminopropoxy)3'methoxyphenyl]-2-propenoic acid ethyl ester." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/71666430449483545434.

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Lu, Yi-Chih, and 呂益誌. "Synthetic studies of the (7''R)-8-[1-(4'-hydroxy-3'-methoxyphenyl)prop-2-en-1-yl]galangin." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/92332011961472886474.

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碩士<br>國立彰化師範大學<br>化學系<br>101<br>(7''R)-8-[1-(4'-Hydroxy-3'-methoxyphenyl)prop-2-en-1-yl]galangin, a new flavonoid isolated from Mexican propolis in 2010, displays preferential cytotoxicity against PANC-1 cells of human pancreatic cell line. First, the preparation of 8-bromo galangin was begun from the commercially available phloroglucinol. The phloroglucinol was converted by methylation and acetylation reactions to give dimethoxyphenyl acetate in two steps overall 49% yield. The dimethoxyphenyl acetate was transformed by Fries rearrangement in presence of AlCl3 to give acetophenone in 58% yiel

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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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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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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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32

tienyaotine and 田耀庭. "Thermal [m+n] cycloadditions of 8,8-Dicyanoheptafulvene with 6-(1',1'-Diethylmethyl)fulvene and 6-(4-Methoxyphenyl)fulvene for room temperature." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/40817011293351667664.

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碩士<br>中國文化大學<br>應用化學研究所<br>94<br>The investigation of this research involves the synthesis and intermolecular [m+n] cycloadditions of the unsymmetrically electron-rich 6-(1,1-Diethylmethyl)fulvene and 6-(4-methoxyphenyl)fulvene with 8,8-dicyaoheptafulvene; designed to establish the experimental analyses of the reactivity, diastereoselectivity, periselectivity, and regioselectivity of these cycloadditions. The experiment uses 1H-NMR, COSY, NOESY, E.I.M.S., H.E.I.M.S.À is judged . The result shows, under the gentle response condition of the room temperature, 8,8-Dicyanoheptafulvene to be 6 - (1

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HUANG, CONG-LONG, та 黃聰龍. "Synthesis and β-adrenoceptor blocking effects of DZBN(4-[ 4'-(2-hydroxy-3-tert-butylaminopropoxy)-3'-methoxyphenyl]-3-buten-2-one)". Thesis, 1993. http://ndltd.ncl.edu.tw/handle/79413869156473123248.

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34

Teng, Chia-Yin, and 滕家吟. "Synthesis and Optoelectronic Properties of Novel Poly(amide-imide)s Bearing N,N’-Di(4-methoxyphenyl)-N,N’-diphenyl- p-phenylenediamine Units." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/b83ncc.

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碩士<br>國立臺北科技大學<br>化學工程研究所<br>103<br>An aromatic secondary amine N,N’-bis(4-methoxyphenyl)-1,4- phenylenediamine (1) was synthesized by condensation of p-anisidine with hydroquinone. Subsequent condensation of compound 1 with p-fluoronitrobenzene resulted in the dinitro compound N,N’-bis(4-nitrophenyl)-N,N’-bis(4-methoxy- phenyl)-1,4-phenylenediamine (2), which was then reduced to the target diamine monomer, N,N’-bis(4-aminophenyl)-N,N’-bis(4-methoxyphenyl)-1,4-phenylene- diamine (3). A new dicarboxylic acid monomer bearing two built-in imide rings, namely N,N’-bis(trimellitimidophenyl)-N,N’-bi

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35

Liao, Chih-Chang, and 廖志彰. "Synthesis and cytotoxicity of 2-(hydroxyphenyl)-6-methyl-1,8-naphthyridin-4-ones and 2-(3-methoxyphenyl)-6-methyl-1,8-naphthyridin-4-one-8-N-oxide." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/94121368727238382567.

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碩士<br>中國醫藥大學<br>藥物化學研究所碩士班<br>98<br>Abstract In the previous study, 2-(3-methoxyphenyl)-6-methyl-1,8-naphthyridin-4-one（LYF-5）was synthesized and found to possess strong cytotoxicity. Because of its low hydrophilicity, an attempt was made to synthesize of its 4-phosphate. Whereas the poor stability proinhibited it from further development . In this study, two kinds of target compounds, including hydroxyl derivatives（IIa-IIc、IIIa、IVa、IVb） and 8-N-oxide（Va）were designed. Condensation of 2-amiopyridine with benzoyl acetates in PPA formed the corresponding pyrido-pyrimidines（5a-5g）. Thermal

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36

Chen, Shao-Yu, та 陳少宇. "（一）Pyrolytic Study of 2-Azido-1-(4-methoxyphenyl)ethanone and2-(2-Azidoethyl)furan（二）Pyrolytic Study of 3-Methyl-2-Cyclohexno[b]furylmethyl Benzoate". Thesis, 2012. http://ndltd.ncl.edu.tw/handle/52556926629861492818.

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碩士<br>國立中山大學<br>化學系研究所<br>100<br>一、Pyrolysis of 2-azido-1-(4-methoxyphenyl)ethanone (69) and 2-(2-azidoethyl)furan (85) gave nitrene intermediate to study. There is 2-(4-methoxybenzoyl)-4-(4- methoxyphenyl)imidazole (81) 、2-(4-methoxybenzoyl)-5-(4-methoxyphenyl) imidazole] (81’)、2,3-di(4-methoxybenzoyl)-5-(4-methoxyphenyl) pyrazine] (82) and 3,5-di(2-furyl) pyridine (92) for pyrolysis products. 二、Pyrolysis of3-methyl-2-cyclohexen[b] furylmethyl benzoate) (50) gave carbene intermediate to study. There is 2,3-dimethylene cyclohexen[b]furan (59) for pyrolysis products.

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37

Yang, Jai Sing, and 楊家欣. "Studies on the Anticancer Mechanisms of 2-(3''-Methoxyphenyl)-6-pyrrolidinyl-4-quinazolinone (HMJ-38) in HL-60 cells and in WEHI-3/BALB/c Leukemia Animal Model." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/51958215335926581992.

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博士<br>中國醫藥大學<br>藥物化學研究所<br>92<br>We previously reported that HMJ-38 was the most potent 2-phenyl-4-quinazolinone derivative in inhibiting tubulin polymerization and showed significant cytotoxicity against several human tumor cell lines. In this study, we studied its cytotoxic effect on HL-60 leukemia cells and underlying mechanisms and investigated the anticancer activity of HMJ-38 in syngeneic BALB/c mice bearing murine WEHI-3 leukemia cells. We first investigated the effects of HMJ-38 on viability, cell cycle and induction of apoptosis in leukemia cell lines (HL-60, U937 and K562

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38

Li, Liang-You, та 李亮佑. "(一) Pyrolytic and Photolytic Studies of 1-（o-methoxyphenyl）-3-phenylprop-2-en-1-one and Its Derivatives (二) Pyrolytic Study of (N-Methyl-2-indolyl)methyl Benzoate". Thesis, 2013. http://ndltd.ncl.edu.tw/handle/62202612707107546857.

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碩士<br>國立中山大學<br>化學系研究所<br>101<br>一、 1-（o-Methoxyphenyl）-3-phenylprop-2-en-1-one（35）、1-（o- allyloxyphenyl）-3-phenylprop-2-en-1-one（37）、3-（o-methoxyphenyl）-3-phenylprop-2-en-1-one（38）、3-（o- allyloxyphenyl）-3-phenylprop-2-en-1-one（39）、1-（o-methoxyphenyl）-3-phenylprop-2-yn-1-one（40）have been studied by means of pyrolysis and photolysis. Under pyrolytic conditions, compounds 35、37 and 40 gave expected product flavone（36）and major product 2-phenylbenzo[b]furan（8）. Compound 38 and 39 gave major product phenanthrene（2）. Under photolytic conditions, compound 35 didn’t give any product. Compound 38 gave

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39

Chen, Hsi-An, and 陳璽安. "(I) Constituents of 2-methoxyphenol from Zingiber officinale (ginger) treat clinical extensively drug resistant Acinetobacter baumannii synergistically by antioxidation properties(II) Constituents from Cinnamomum kotoense as human Lon protease inhibito." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/16440059190110162960.

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碩士<br>高雄醫學大學<br>香粧品學系碩士班<br>97<br>(I) Bacterial resistance to antibiotics is a major therapeutic problem in decades. The extensively drug resistant Acinetobacter baumanii (XDRAB) causes serious nosocomial infections worldwide, particularly at intensive care units (ICUs). Several pure compounds from the rhizomes of Zingiber officinale have been shown the various effects on human such as anti-tumor and anti-inflammation. However, their antimicrobial activities have not been reported on clinical bacterial isolates. The aim of this study was to find the components from ginger with novel anti-exten

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40

chieh, huang ming, та 黃明傑. "拉電子基取代之8,8-Dicyanoheptafulvene和不對稱單取代之6-(4-Methoxyphenyl)fulevne,6-(4-Nitrophenyl)fulvene和6-Phenylfulvene進行加熱[m+n]環化加成反應之研究". Thesis, 2005. http://ndltd.ncl.edu.tw/handle/81331621539755205044.

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碩士<br>中國文化大學<br>應用化學研究所<br>93<br>The investigation of this research involves the synthesis and intermolecular [m+n] cycloadditions of the unsymmetrically electron-rich 6-monosubstituted 6-phenylfulvene (1n) 6-(4-Methoxyphenyl)fulvene, 6-(4-Nitrophenyl)fulvene with 8,8-dicyaoheptafulvene (8a); designed to establish the experimental analyses of the reactivity, diastereoselectivity, periselectivity, and regioselectivity of these cycloadditions. The cycloaddition reaction of 8,8-dicyanoheptafulvene (8a) with 6-phenylfulvene (1n) at room temperature gave the anti-endo-[6+4] cycloadducts 21n/21n’

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41

christina та 陳怡婷. "拉電子基取代之8,8-dicyanoheptafulvene和給電子基不對稱“單”取代之6-(4-methoxyphenyl)fulvene在氯仿迴流下進行[m+n]環化加成反應之研究". Thesis, 2006. http://ndltd.ncl.edu.tw/handle/72175321628004330312.

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碩士<br>中國文化大學<br>應用化學研究所<br>94<br>The investigation of this research involves the synthesis and intermolecular [m+n] cycloadditions of the unsymmetrically electron-rich 6-monosubstituted 6-(4-methoxyphenyl)fulvene with 8,8-dicyaoheptafulvene ; designed to establish the experimental analyses of the reactivity, diastereoselectivity, periselectivity, and regioselectivity of these cycloadditions. The cycloaddition reaction of 8,8-dicyanoheptafulvene with 6-(4-methoxyphenyl)fulvene at room temperature gave the anti-endo-[6+4] cycloadducts 23n/23n’(1:1 ratio) and. The present results show that these

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42

(7360475), Sabyasachy Mistry. "MASS SPECTROMETRIC DETECTION OF INDOPHENOLS FROM THE GIBBS REACTION FOR PHENOLS ANALYSIS." Thesis, 2020.

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<p><a></a><a></a><a></a><a></a><a></a><a></a><a></a><a></a><a></a><a></a><a>ABSTRACT</a></p> <p>Phenols are ubiquitous in our surroundings including biological molecules such as L-Dopa metabolites, food components, such as whiskey and liquid smoke, etc. This dissertation describes a new method for detecting phenols, by reaction with Gibbs reagent to form indophenols, followed by mass spectrometric detection. Unlike the standard Gibbs reaction which uses a colorimetric approach, the use of mass spectrometry allows for simultaneous detection of differently substituted phenols. The procedure is

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