Relevant bibliographies by topics / Hydroxyanthraquinone – Synthesis

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Academic literature on the topic 'Hydroxyanthraquinone – Synthesis'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Hydroxyanthraquinone – Synthesis"

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Yenilmez Çiftçi, Gönül, Nagihan Bayık, Esra Tanrıverdi Eçik, Elif Şenkuytu, Maşuk Akşahin, and Tuba Yıldırım. "Synthesis of the first 2-hydroxyanthraquinone substituted cyclotriphosphazenes and their cytotoxic properties." New Journal of Chemistry 44, no. 39 (2020): 16733–40. http://dx.doi.org/10.1039/d0nj02723e.

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New 2-hydroxyanthraquinone based cyclotriphosphazenes were prepared and their cytotoxic effects were investigated in MCF-7 (breast cancer), MCF-12A (normal breast epithelium), DLD-1 (colon cancer), and CD-18Co (normal colon epithelium) cell lines.
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Zhu, Li, Wenfeng Wang, Junwei Miao, Xu Yin, Xiufang Hu, and Yaofeng Yuan. "Synthesis, NMR and computational studies on tautomerism of dichloroacetate of hydroxyanthraquinone." Journal of Molecular Structure 1141 (August 2017): 462–68. http://dx.doi.org/10.1016/j.molstruc.2017.03.101.

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Kudrevatykh, Alexandra A., and Lyubov S. Klimenko. "Synthesis and properties of halogen-containing macrocyclic anthraquinone imines – chemosensors for metal cations." Yugra State University Bulletin 16, no. 2 (2020): 50–56. http://dx.doi.org/10.17816/byusu2020250-56.

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New crown-containing imines of 1-hydroxyanthraquinone with chlorine and fluorine atoms in the anthraquinone nucleus were synthesized. For the first time, the thermal and photochemical stages of synthesis are carried out in the solid state (without a solvent). The features of complexation of new chemosensors with cations of alkaline and alkaline earth metals were studied by spectrophotometry. It is shown that the introduction of halogen atoms in the anthraquinone nucleus leads to a significant spectral response. The obtained compounds are tested as components of test systems for visual determin
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Yenilmez Çiftçi, Gönül, Gizem Demir, Elif Şenkuytu, Esra Tanrıverdi Eçik, Masuk Aksahin, and Tuba Yıldırım. "2-Hydroxyanthraquinone substituted cyclotriphosphazenes: Synthesis and cytotoxic activities in cancer cell lines." Inorganica Chimica Acta 514 (January 2021): 120005. http://dx.doi.org/10.1016/j.ica.2020.120005.

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5

Nguyen, Trang, Ramesh Pandey, Prakash Parajuli, et al. "Microbial Synthesis of Non-Natural Anthraquinone Glucosides Displaying Superior Antiproliferative Properties." Molecules 23, no. 9 (2018): 2171. http://dx.doi.org/10.3390/molecules23092171.

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Anthraquinones, naturally occurring bioactive compounds, have been reported to exhibit various biological activities, including anti-inflammatory, antiviral, antimicrobial, and anticancer effects. In this study, we biotransformed three selected anthraquinones into their novel O-glucoside derivatives, expressing a versatile glycosyltransferase (YjiC) from Bacillus licheniformis DSM 13 in Escherichia coli. Anthraflavic acid, alizarin, and 2-amino-3-hydroxyanthraquinone were exogenously fed to recombinant E. coli as substrate for biotransformation. The products anthraflavic acid-O-glucoside, aliz
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Cambie, RC, SE Holroyd, DS Larsen, PS Rutledge, and PD Woodgate. "Experiments Directed Towards the Synthesis of Anthracyclinones. XVI. Tin(IV)- and Titanium(IV)-Mediated Cyclizations of ortho-Allyl-Substituted Homochiral Hydroxyanthraquinone Dioxolans." Australian Journal of Chemistry 45, no. 10 (1992): 1589. http://dx.doi.org/10.1071/ch9921589.

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Tin(IV) chloride and titanium(IV) chloride mediated cyclizations of the ortho-allyl-substituted homochiral hydroxyanthraquinone acetals (7)-(10), prepared by optimized redictive Claisen rearrangements, have afforded monochloro and dichloro tetracyclic products, the tereochemistry of which has been assigned by using n.m.r. techniques. An Sn2-like process in which the dioxolan ring is maintained as an ion pair intermediate is favoured when either tin(IV) chloride or titanium(IV) chloride is used at -78�. Thereafter the direction of addition of chloride at C9 is largely governed by the orientatio
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Sirazhetdinova, Nafisa S., Victor A. Savelyev, Dmitry S. Baev, et al. "Synthesis, characterization and anticancer evaluation of nitrogen-substituted 1-(3-aminoprop-1-ynyl)-4-hydroxyanthraquinone derivatives." Medicinal Chemistry Research 30, no. 8 (2021): 1541–56. http://dx.doi.org/10.1007/s00044-021-02754-1.

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Zhao, Li-Ming, Feng-Yan Ma, Hai-Shan Jin, Shilong Zheng, Qiu Zhong, and Guangdi Wang. "Design and synthesis of novel hydroxyanthraquinone nitrogen mustard derivatives as potential anticancer agents via a bioisostere approach." European Journal of Medicinal Chemistry 102 (September 2015): 303–9. http://dx.doi.org/10.1016/j.ejmech.2015.08.006.

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Frąckowiak, Anna, Przemysław Skibiński, Wiesław Gaweł, Ewa Zaczyńska, Anna Czarny, and Roman Gancarz. "Synthesis of glycoside derivatives of hydroxyanthraquinone with ability to dissolve and inhibit formation of crystals of calcium oxalate. Potential compounds in kidney stone therapy." European Journal of Medicinal Chemistry 45, no. 3 (2010): 1001–7. http://dx.doi.org/10.1016/j.ejmech.2009.11.042.

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CAMBIE, R. C., S. E. HOLROYD, D. S. LARSEN, P. S. RUTLEDGE, and WOODGATE P. D. WOODGATE P. D. "ChemInform Abstract: Experiments Directed Towards the Synthesis of Anthracyclinones. Part 16. Tin(IV)- and Titanium(IV)-Mediated Cyclizations of ortho-Allyl- Substituted Homochiral Hydroxyanthraquinone Dioxolans." ChemInform 24, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199306306.

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Dissertations / Theses on the topic "Hydroxyanthraquinone – Synthesis"

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Gomez, Galeno Jorge E. "Part I, Aromatic annelation : synthesis of naphthalenes ; Part II, C-glycosyl anthraquinone synthesis : total synthesis of vineomycinone B2 methyl ester." Thesis, 1990. http://hdl.handle.net/10125/9496.

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Books on the topic "Hydroxyanthraquinone – Synthesis"

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Ezenwafor, Ephraim Ifeanyi Ihechukwu. The synthesis and properties of derivatives of 1-amino-4-hydroxy anthraquinone: The synthesis ofthiolated derivatives of 1-amino-4-hydroxyanthraquinone and a study of their application, dyeing and fastness properties on synthetic-polymer fibres. 1985.

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