Relevant bibliographies by topics / Dihydrophenanthrene

Contents

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

Academic literature on the topic 'Dihydrophenanthrene'

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

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Journal articles on the topic "Dihydrophenanthrene"

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Pettit, George R., Sheo Bux Singh, Margaret L. Niven, and Jean M. Schmidt. "Cell growth inhibitory dihydrophenanthrene and phenanthrene constituents of the african tree Combretum caffrum." Canadian Journal of Chemistry 66, no. 3 (1988): 406–13. http://dx.doi.org/10.1139/v88-071.

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Combretum caffrum, a tree in the family Combretaceae, has been found to contain three 9,10-dihydrophenanthrenes (6,7-dihydroxy-2,3,4-trimethoxy; 7-hydroxy-2,3,4,6-tetramethoxy; and 2,7-dihydroxy-3,4,6-trimethoxy) that inhibit (ED50 2.2, 2.8, and 2.6 μg/mL) growth of the murine lymphocytic leukemia cell line. One phenanthrene (7-hydroxy-2,3,4,6-tetramethoxy) was also isolated with similar (ED50 2.0 μg/mL) activity. Structures for each of these substances, including a dihydrophenanthrene (2-hydroxy-3,4,6,7-tetramethoxy-9,10-dihydrophenanthrene), were determined by detailed high resolution nuclea
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2

Butts, CP, L. Eberson, KL Fulton, MP Hartshorn, and WT Robinson. "Photochemical Nitration by Tetranitromethane. XXXII. Adduct Formation in the Photochemical Reaction of Phenanthrene and Tetranitromethane." Australian Journal of Chemistry 49, no. 4 (1996): 469. http://dx.doi.org/10.1071/ch9960469.

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Photolysis of the phenanthrene/tetranitromethane charge-transfer complex yields the triad of phenanthrene radical cation, nitrogen dioxide, and trinitromethanide ion. Recombination of this triad in dichloromethane at 20° gives 9-nitrophenanthrene (1), trans-10-trinitromethyl-9,10-dihydrophenanthren-9-yl nitrate (2a), trans-9-nitro-10-trinitromethyl-9,10-dihydrophenanthrene (2b), and trans-10-trinitromethyl-9,10-dihydrophenanthren-9-ol (2c). Adduct formation is partially suppressed when trifluoroacetic acid (0.7 M) is added to the dichloromethane solvent at 20°, the major product identified bei
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3

Bisoli, Eder, Talita Vilalva Freire, Nídia Cristiane Yoshida, et al. "Cytotoxic Phenanthrene, Dihydrophenanthrene, and Dihydrostilbene Derivatives and Other Aromatic Compounds from Combretum laxum." Molecules 25, no. 14 (2020): 3154. http://dx.doi.org/10.3390/molecules25143154.

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The chemical investigation of the roots and stems of Combretum laxum yielded a new dihydrostilbene derivative, 4′-hydroxy-3,3′,4-trimethoxy-5-(3,4,5-trimethoxyphenoxy)-bibenzyl (1), two phenanthrenes (2–3), and three dihydrophenanthrenes (4–6), along with one lignan, three triterpenoids, one aurone, one flavone, one naphthoquinone, and two benzoic acid derivatives. Their structures were determined by 1D and 2D nuclear magnetic resonance (NMR) spectroscopic techniques and/or mass spectrometry data. The occurrence of dihydrostilbenoid, phenanthrene and dihydrophenanthrene derivatives is unpreced
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Delle Monache, Franco, Giuliano Delle Monache, Julianna F. Cavalcanti, and Rogerio M. Pinheiro. "An unexpected dihydrophenanthrene from." Tetrahedron Letters 28, no. 5 (1987): 563–66. http://dx.doi.org/10.1016/s0040-4039(00)95782-4.

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Jones, P. G. "9,10-Dihydrophenanthrene-4,5-dimethanol." Acta Crystallographica Section C Crystal Structure Communications 48, no. 12 (1992): 2245–47. http://dx.doi.org/10.1107/s0108270192003962.

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Shi, Yong-gang, Soren K. Mellerup, Kang Yuan, et al. "Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers." Chemical Science 9, no. 15 (2018): 3844–55. http://dx.doi.org/10.1039/c8sc00560e.

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Greca, Marina Della, Antonio Fiorentino, Antonio Molinaro, Pietro Monaco, and Lucio Previtera. "9,10-Dihydrophenanthrene Glucosides fromJuncus effusus." Natural Product Letters 6, no. 2 (1995): 111–17. http://dx.doi.org/10.1080/10575639508044098.

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Dijoux-Franca, M. Geneviève, Diderot Noungoué Tchamo, Bruno Cherel, Max Cussac, Etienne Tsamo, and Anne-M. Mariotte. "New Dihydrophenanthrene and Phenyldihydroisocoumarin Constituents ofTremaorientalis." Journal of Natural Products 64, no. 6 (2001): 832–35. http://dx.doi.org/10.1021/np000275s.

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Lewis, Frederick D., Todd L. Kurth, and Rajdeep S. Kalgutkar. "A push–pull 4a,4b-dihydrophenanthrene." Chemical Communications, no. 15 (2001): 1372–73. http://dx.doi.org/10.1039/b104510p.

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10

Sekine, Toshikazu, Nobuyaki Fukasawa, Isamu Murakoshi, and Nijsiri Ruangrungsi. "A 9,10-dihydrophenanthrene from Asparagus racemosus." Phytochemistry 44, no. 4 (1997): 763–64. http://dx.doi.org/10.1016/s0031-9422(96)00579-1.

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Dissertations / Theses on the topic "Dihydrophenanthrene"

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Munam, Abdul. "Chemistry of dihydrophenanthrene ketal and its application in polymer curing." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0020/MQ48505.pdf.

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古樹隆. "9,10-dihydrophenanthrene衍生物的Ring-strain效應對發光性質的影響及應用在有機發光二極體的探討". Thesis, 2005. http://ndltd.ncl.edu.tw/handle/98007596557922953359.

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Mao-Chia, Yuan, and 袁茂嘉. "Synthesis of Dihydrophenanthrenes with Antitumor Activity." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/51265054666742312170.

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碩士<br>中國文化大學<br>應用化學研究所<br>97<br>The Chinese herbal medicine “Shi-Hu” is prepared from the dried stalks of Dendrobium species and has been used for treatment of stomach, liver, spleen, lung, kidney, and eyes disease. In Taiwan, Ephemerantha lonchophylla is also used as a source of “Shi-Hu”. Recently, 2,5,6,7-tetramethoxy-9,10-dihydrophenanthren-1-ol and 2,3,4,7-tetramethoxy-9,10-dihydrophenanthrene were isolated from Ephemerantha lonchophylla and showed strong antitumor activity. It prompted us to synthesize these dihydrophenanthrenes and their derivatives. In this thesis, a variety of ben
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Book chapters on the topic "Dihydrophenanthrene"

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Seigler, David S. "2-Pyrones, Stilbenes, Dihydrophenanthrenes, and Xanthones." In Plant Secondary Metabolism. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4913-0_10.

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Qi, Jiaxin, Di Zhou, Gang Chen, and Ning Li. "Bioactive dihydrophenanthrenes from plants." In Bioactive Natural Products. Elsevier, 2022. http://dx.doi.org/10.1016/b978-0-323-91099-6.00002-5.

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Conference papers on the topic "Dihydrophenanthrene"

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Yamari, Imane, Suraj N. Mali, Ossama Abchir, et al. "In Silico Investigations of Dihydrophenanthrene Derivatives as Potential Inhibitors of SARS-CoV-2." In International Electronic Conference on Medicinal Chemistry. MDPI, 2022. http://dx.doi.org/10.3390/ecmc2022-13293.

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Hansakul, P., K. Aree, W. Duangprompo, and A. Itharat. "Caspase-dependent apoptosis induced by 5,6-dihydroxy-2,4-dihydrophenanthrene in human lung adenocarcinoma A549 cells." In GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608134.

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Haidar, Samer, Annika Meyers, and Joachim Jose. "Design and Development of 9,10-Dihydrophenanthrene Derivatives as Inhibitors of Human Protein Kinase CK2." In 2nd International Electronic Conference on Medicinal Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecmc-2-a020.

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4

Aminah, N. S., A. Yulvia, and M. Tanjung. "Methyl-3,4-dihydroxybenzoate and 9-10-dihydrophenanthrene-2,4,7-triol two phenolic compounds from Dioscorea alata L. and their antioxidant activity." In 6TH INTERNATIONAL CONFERENCE AND WORKSHOPS ON BASIC AND APPLIED SCIENCES. Author(s), 2017. http://dx.doi.org/10.1063/1.5004327.

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Sension, Roseanne J., Stephen T. Repinec, Arpad Z. Szarka, and Robin M. Hochstrasser. "Ultrafast Photoreactions of cis-Stilbene." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/up.1992.fc23.

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Time resolved spectroscopic studies of the photoisomerization reactions of cis-stilbene in solution have provided a great deal of information on these simple reactions (1-3). Transient absorption (1,2) and fluorescence (3) experiments have demonstrated that the initially created electronically excited cis-stilbene population (cis*) persists for 0.5 to 1.5 ps in room temperature solution-phase environments. Polarized transient absorption experiments and time-resolved fluorescence experiments indicate that during this time the cis* molecules retain most of the energy of the incident photon and a
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Reports on the topic "Dihydrophenanthrene"

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Sritularak, Boonchoo, Kittisak Likhitwitayawuid, Pithi Chanvorachote, and Varisa Pongrakhananon. Cytotoxic constituents from Dendrobium spp. : Final report. Chulalongkorn University, 2014. https://doi.org/10.58837/chula.res.2014.28.

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The MeOH extracts of Dendrobium pullchellum Roxb. Ex Lind1. And D. ellipsophyllum Tang &amp; wang (Orchidaceae) showed significant cytotoxic activity against human lung cancer cells. Phytochemical study of the whole plant of D. pullchellum Roxb. Ex Lind1 led to the isolation of seven phenolic compounds, namely, chrysotobibenzyl, chrysotoxine, crepidatin, moscatilin, fimbriatone, (-) –shikimic acid and liriodendrin. The whole plant of D. ellipsophyllum Tang &amp; wang yielded ten phenolic compounds indluding moscatilin, 5,7-dihydroxy-chromen-4-one, 4,5-dihydroxy-2,3-dimethoxy-9,10-dihydrophenan
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You might also be interested in the extended bibliographies on the topic 'Dihydrophenanthrene' for particular source types:
Journal articles
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