Relevant bibliographies by topics / Phenanthrenyl amine

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Phenanthrenyl amine'

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

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Journal articles on the topic "Phenanthrenyl amine"

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Afonso, Carlos A. M., and J. P. S. Farinha. "Synthesis of 4-aryl-butylamine Fluorescent Probes." Journal of Chemical Research 2002, no. 11 (2002): 584–86. http://dx.doi.org/10.3184/030823402103170871.

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A short synthesis of the fluorescent probes 4-(9-anthracenyl)butyl amine (three steps), 4-(9-phenanthrenyl)butyl amine (three steps) and 4-(1-pyrenyl)butyl amine (two steps) without chromatographic purification is described.
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Ram, Naresh Yadav, Banik Indrani та Krishna Banik Bimal. "Microwave-assisted novel stereoselective synthesis of bis-β-lactams with 2,7-phenanthrenyl imines". Journal of Indian Chemical Society Vol. 95, Nov 2018 (2018): 1377–80. https://doi.org/10.5281/zenodo.5652757.

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Department of Chemistry, Faculty of Engineering &amp; Technology, Veer Bahadur Singh Purvanchal University, Jaunpur-222 003, Uttar Pradesh, India Department of Chemistry, University of Texas-Pan American,1201 W. University Dr., Edinburg, TX 78539, USA The University of Texas M. D. Anderson Cancer Center, Department of Molecular Pathology, 1515 Holcombe Blvd, Houston, TX 77030, USA Community Health System of South Texas, 3135 South Sugar Road, Edinburg, TX 78539, USA E-mail: bimalbanik10@gmail.com, bimal.banik@chsst.org <em>Manuscript received 01 October 2018, accepted 02 November 2018</em> Mic
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Šindelář, Karel, Jiří Holubek, Miroslav Ryska, Ivan Koruna, and Miroslav Protiva. "5-Substituted and 5,7-disubstituted 5,7-dihydrodibenzo[c,e]thiepins and the corresponding S-oxygenated compounds: Alkylamines, carboxylic acids, and carboxamides; synthesis and pharmacological screening." Collection of Czechoslovak Chemical Communications 51, no. 12 (1986): 2848–68. http://dx.doi.org/10.1135/cccc19862848.

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Reaction of 5,7-dihydrodibenzo[c,e]thiepin (I) with n-butyllithium resulted in the partial sulfur extrusion and in the formation of the 9,10-dihydrophenanthrene-9-thiolate anion (B). Its further transformations (by hydrolysis, aminoalkylation and spontaneous dehydrogenation) led to phenanthrene-9-thiol (IX), the corresponding disulfide X, and the S-(2-dimethylaminoethyl) derivatives XI and XIV. Reactions of 5-chloro-5,7-dihydrodibenzo[c,e]thiepin (II) with the corresponding Grignard reagents were only a poor source of the amines III and IV. Reaction of the sulfoxide XVIII with n-butyllithium o
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Jiang, Guanyu, Xinduo Sun, Fanrui Zhou, Kun Liang, and Qian Chen. "Chiral Quaternary Ammoniums Derived from Dehydroabietylamine: Synthesis and Application to Alkynylation of Isatin Derivatives Catalyzed by Silver." Catalysts 11, no. 12 (2021): 1479. http://dx.doi.org/10.3390/catal11121479.

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Abietic acid and its derivatives have broadly been used in fine chemicals and are renewable resources. Its inherent chiral rigid tricyclic phenanthrene skeleton is unique. Its utilities in asymmetric catalysis remain to be explored. A series new amide-type chiral quaternary ammoniums bearing dehydroabietylamine were designed, and prepared by two convenient steps. Acylation of dehydroabietylamine with bromoacetyl chloride afforded amide holding bromoacetyl group in higher yields using triethyl amine as base. Subsequent quaternization reaction gave the desired amide-type chiral quaternary ammoni
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Estévez, Juan C., M. Carmen Villaverde, Ramon J. Estévez, Julio A. Seuas, and Luis Castedo. "New total synthesis of phenanthrene alkaloids." Canadian Journal of Chemistry 68, no. 6 (1990): 964–68. http://dx.doi.org/10.1139/v90-151.

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We describe a new synthesis of phenanthrene alkaloids based on the photocyclization of stilbene compounds prepared by a simple, efficient new method. It allows the preparation of phenanthrene compounds with a primary amine group in their side chain. Keywords: alkaloid, phenanthrene, stilbene, photocyclization.
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Lewis, Frederick D., and Bliss E. Cohen. "Solvent-Dependent Behavior of Phenanthrene-Amine Intramolecular Exciplexes." Journal of Physical Chemistry 98, no. 41 (1994): 10591–97. http://dx.doi.org/10.1021/j100092a033.

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Guédouar, Habiba, Faouzi Aloui, and Bechir Ben hassine. "Benzo[c]phenanthrene derivatives: Synthesis, optical properties and cytotoxic activity." JOURNAL OF ADVANCES IN CHEMISTRY 12, no. 9 (2016): 4404–12. http://dx.doi.org/10.24297/jac.v12i9.6706.

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A new benzo[c]phenanthrene ketone has been synthesized through Heck coupling and oxidative photocyclization. The optical properties of the target tetracyclic system were also investigated by UV-visible absorption and photoluminescence spectroscopy and an emission in the visible region was observed. The tetracyclic ketone has been reacted with primary amines in the presence of Lewis acid followed by NaBH4 reduction to provide new polyaromatic secondary amines in good yields and purity. All the synthesized new compounds were identified and characterized through a combination of nuclear magnetic
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Sun, Mingjie, Xinyang Chen, Zichao Feng, Guobo Deng, Yuan Yang, and Yun Liang. "A Catellani and retro-Diels–Alder strategy to access 1-amino phenanthrenes via ortho- and interannular C–H activation of 2-iodobiphenyls." Organic Chemistry Frontiers 8, no. 23 (2021): 6535–40. http://dx.doi.org/10.1039/d1qo01103k.

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9

Al-Moubarak, Ehab, Holly A. Shiels, Yihong Zhang, et al. "Inhibition of the hERG potassium channel by phenanthrene: a polycyclic aromatic hydrocarbon pollutant." Cellular and Molecular Life Sciences 78, no. 23 (2021): 7899–914. http://dx.doi.org/10.1007/s00018-021-03967-8.

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AbstractThe lipophilic polycyclic aromatic hydrocarbon (PAH) phenanthrene is relatively abundant in polluted air and water and can access and accumulate in human tissue. Phenanthrene has been reported to interact with cardiac ion channels in several fish species. This study was undertaken to investigate the ability of phenanthrene to interact with hERG (human Ether-à-go-go-Related Gene) encoded Kv11.1 K+ channels, which play a central role in human ventricular repolarization. Pharmacological inhibition of hERG can be proarrhythmic. Whole-cell patch clamp recordings of hERG current (IhERG) were
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Jhulki, Samik, Abhaya Kumar Mishra, Avijit Ghosh, Tahsin J. Chow, and Jarugu Narasimha Moorthy. "Deep blue-emissive bifunctional (hole-transporting + emissive) materials with CIEy ∼ 0.06 based on a ‘U’-shaped phenanthrene scaffold for application in organic light-emitting diodes." Journal of Materials Chemistry C 4, no. 39 (2016): 9310–15. http://dx.doi.org/10.1039/c6tc02615j.

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Phenanthrenes functionalized two-fold at 3,6 positions by fluorophoric amines, i.e., PTPA, PDPA and PCZL, serve as very good bifunctional materials (HTM + EM) with deep blue emission in simple double layer OLED devices.
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Dissertations / Theses on the topic "Phenanthrenyl amine"

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Ouellette, Mélanie. "Gas-phase Ion Chemistry of Hydroxy and Amino-substituted Interstellar Polycyclic Aromatic Hydrocarbons and Protonated Polycyclic Aromatic Hydrocarbons." Thesis, Université d'Ottawa / University of Ottawa, 2014. http://hdl.handle.net/10393/31349.

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The gas-phase ion chemistry of hydroxyl- and amino-substituted polycyclic aromatic hydrocarbons (PAHs) and their protonated counterparts were studied using mass spectrometry. Ions were generated using an electron ionization (EI) source and the unimolecular chemistry of metastable ions was studied by performing mass-analysed ion kinetic energy spectrometry (MIKES) experiments with a magnetic sector tandem mass spectrometer. Collision-induced dissociation (CID) experiments were used in conjunction with MIKES experiments to determine ion structure. The ten molecules studied were: 1-naphthol, 2-na
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Li, Cang-Xian, and 李倉賢. "Reactions of diquinone and tertiary amines produced phenanthrene oxide derivatives via palladium catalyzed carbon-hydrogen bond activation." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/69bw34.

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碩士<br>國立中興大學<br>化學系所<br>107<br>In this work, both diquinone, having two amido groups at opposite positions, and 3° amine as starting materials were used to carry out in an one-pot reaction in presence of palladium salt as catalyst. This catalytic reaction were screened with various reaction conditions to find out the optimized combinations of variable. A new compound 7b was obtained while a 3° amine (NBu3) had been used. The crystal structure of 7b was confirmed by the single crystal X-ray determining process. The structure of 7b reveals that it is having a main framework of 1,4,5,8-phenanthre
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Book chapters on the topic "Phenanthrenyl amine"

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Taber, Douglass F. "Alkaloid Synthesis: Penaresidin A (Subba Reddy), Allokainic Acid (Saicic), Sedacryptine (Rutjes), Lepistine (Yokoshima/Fukuyama), Septicine (Hanessian), Lyconadin C (Dai)." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0058.

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Penaresidin A 3, isolated from the Okinawan marine sponge Penares sp., is a potent activator of actomyosin ATPase. B. V. Subba Reddy of the Indian Institute of Chemical Technology prepared (Tetrahedron Lett. 2014, 55, 49) the azetidine ring of 3 by mesyl­ation of the hydroxy sulfonamide 2, derived from 1, followed by cyclization. Allokainic acid 6 has become a useful tool for neurological studies. Radomir N. Saicic of the University of Belgrade found (Org. Lett. 2014, 16, 34) that the Tsuji–Trost cyclization of 4 to 5 proceeded with high diastereoselectivity, presumably by way of the enamine o
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Journal articles
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