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Relevant bibliographies by topics / Organoruthenium compounds

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Academic literature on the topic 'Organoruthenium compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 20 February 2023

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Journal articles on the topic "Organoruthenium compounds"

1

Trobec, Tomaž, Kristina Sepčić, Monika Cecilija Žužek, Jerneja Kladnik, Nina Podjed, Catarina Cardoso Páscoa, Iztok Turel, and Robert Frangež. "Fine Tuning of Cholinesterase and Glutathione-S-Transferase Activities by Organoruthenium(II) Complexes." Biomedicines 9, no. 9 (September 16, 2021): 1243. http://dx.doi.org/10.3390/biomedicines9091243.

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Cholinesterases (ChEs) show increased activities in patients with Alzheimer’s disease, and remain one of the main therapeutic targets for treatment of this neurodegenerative disorder. A library of organoruthenium(II) complexes was prepared to investigate the influence of their structural elements on inhibition of ChEs, and on another pharmacologically important group of enzymes, glutathione S-transferases (GSTs). Two groups of organoruthenium(II) compounds were considered: (i) organoruthenium(II) complexes with p-cymene as an arene ligand, and (ii) organoruthenium(II) carbonyl complexes as CO-

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2

Chow, Mun Juinn, Cynthia Licona, Giorgia Pastorin, Georg Mellitzer, Wee Han Ang, and Christian Gaiddon. "Structural tuning of organoruthenium compounds allows oxidative switch to control ER stress pathways and bypass multidrug resistance." Chemical Science 7, no. 7 (2016): 4117–24. http://dx.doi.org/10.1039/c6sc00268d.

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Varying the arene ligand on organoruthenium compounds induced the differential activation of ER stress pathways, leading to non-apoptotic programmed cell death and bypassing drug resistance mechanisms.

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3

Shakil, Md Salman, Shahida Parveen, Zohaib Rana, Fearghal Walsh, Sanam Movassaghi, Tilo Söhnel, Mayur Azam, et al. "High Antiproliferative Activity of Hydroxythiopyridones over Hydroxypyridones and Their Organoruthenium Complexes." Biomedicines 9, no. 2 (January 27, 2021): 123. http://dx.doi.org/10.3390/biomedicines9020123.

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Hydroxypyr(id)ones are a pharmaceutically important class of compounds that have shown potential in diverse areas of drug discovery. We investigated the 3-hydroxy-4-pyridones 1a–1c and 3-hydroxy-4-thiopyridones 1d–1f as well as their Ru(η6-p-cymene)Cl complexes 2a–2f, and report here the molecular structures of 1b and 1d as determined by X-ray diffraction analysis. Detailed cell biological investigations revealed potent cytotoxic activity, in particular of the 3-hydroxy-4-thiopyridones 1d–1f, while the Ru complexes of both compound types were less potent, despite still showing antiproliferativ

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4

Mondal, Ashaparna, and Priyankar Paira. "Synthesis and Biological Evaluations of Organoruthenium Scaffolds: A Comprehensive Update." Current Organic Synthesis 15, no. 2 (April 24, 2018): 179–207. http://dx.doi.org/10.2174/1570179414666170703143049.

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Background: Currently ruthenium complexes are immerging as effective anticancer agents due to their less toxicity, better antiproliferative and antimetastatic activity, better stability in cellular environment and most importantly variable oxidation and co-ordination states of ruthenium allows binding this molecule with a variety of ligands. So in past few years researchers have shifted their interest towards organoruthenium complexes having good fluorescent profile that may be applicable for cancer theranostics. Nowadays, photodynamic therapy has become more acceptable because of its easy and

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5

Nogueira, Luciano J., Maria A. de Resende, Sheila R. Oliveira, Maria Helena de Araújo, Thais F. F. Magalhães, Milena B. de Oliveira, Cleide V. B. Martins, Miriam T. P. Lopes, Ana C. Araújo e Silva, and Claudio L. Donnici. "In vitro susceptibility of Aspergillus spp. to dithiocarbamate organoruthenium compounds." Mycoses 54, no. 5 (June 14, 2010): e323-e329. http://dx.doi.org/10.1111/j.1439-0507.2010.01914.x.

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6

Parveen, Shahida, Kelvin K. H. Tong, Muhammad Khawar Rauf, Mario Kubanik, Muhammad Ashraf Shaheen, Tilo Söhnel, Stephen M. F. Jamieson, Muhammad Hanif, and Christian G. Hartinger. "Coordination Chemistry of Organoruthenium Compounds with Benzoylthiourea Ligands and their Biological Properties." Chemistry – An Asian Journal 14, no. 8 (February 14, 2019): 1262–70. http://dx.doi.org/10.1002/asia.201801798.

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7

Nagy, Eszter Marta, and Dolores Fregona. "Critical comment on: ‘In vitro susceptibility of Aspergillus spp. to dithiocarbamate organoruthenium compounds’." Mycoses 55, no. 1 (August 8, 2011): 101. http://dx.doi.org/10.1111/j.1439-0507.2011.02085.x.

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8

Gomathi, Asaithambi, Paranthaman Vijayan, Periasamy Viswanathamurthi, Shanmugam Suresh, Raju Nandhakumar, and Takeshi Hashimoto. "Organoruthenium(II) compounds with pyridyl benzoxazole/benzthiazole moiety: studies on DNA/protein binding and enzyme mimetic activities." Journal of Coordination Chemistry 70, no. 10 (March 30, 2017): 1645–66. http://dx.doi.org/10.1080/00958972.2017.1309649.

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9

Cuccioloni, Massimiliano, Valentina Cecarini, Laura Bonfili, Riccardo Pettinari, Alessia Tombesi, Noemi Pagliaricci, Laura Petetta, Mauro Angeletti та Anna Maria Eleuteri. "Enhancing the Amyloid-β Anti-Aggregation Properties of Curcumin via Arene-Ruthenium(II) Derivatization". International Journal of Molecular Sciences 23, № 15 (5 серпня 2022): 8710. http://dx.doi.org/10.3390/ijms23158710.

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Alzheimer’s disease (AD) is a fatal neurodegenerative disorder associated with severe dementia, progressive cognitive decline, and irreversible memory loss. Although its etiopathogenesis is still unclear, the aggregation of amyloid-β (Aβ) peptides into supramolecular structures and their accumulation in the central nervous system play a critical role in the onset and progression of the disease. On such a premise, the inhibition of the early stages of Aβ aggregation is a potential prevention strategy for the treatment of AD. Since several natural occurring compounds, as well as metal-based mole

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10

Movassaghi, Sanam, Euphemia Leung, Muhammad Hanif, Betty Y. T. Lee, Hannah U. Holtkamp, Jason K. Y. Tu, Tilo Söhnel, Stephen M. F. Jamieson, and Christian G. Hartinger. "A Bioactive l-Phenylalanine-Derived Arene in Multitargeted Organoruthenium Compounds: Impact on the Antiproliferative Activity and Mode of Action." Inorganic Chemistry 57, no. 14 (June 27, 2018): 8521–29. http://dx.doi.org/10.1021/acs.inorgchem.8b01187.

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Dissertations / Theses on the topic "Organoruthenium compounds"

1

Yang, San-ming. "Synthesis and characterization of some organoruthenium complexes containing 1,4,7-trimethyl-1,4,7-triazacyclononane." Click to view the E-thesis via HKUTO, 1997. http://sunzi.lib.hku.hk/hkuto/record/B42574699.

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2

Choi, Mei-yuk. "Synthesis and characterization of some organoruthenium complexes with macrocyclic amine ligands /." Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B20667978.

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3

蔡美玉 and Mei-yuk Choi. "Synthesis and characterization of some organoruthenium complexes with macrocyclic amine ligands." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1999. http://hub.hku.hk/bib/B31220654.

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4

Sishta, Chand. "The coordination chemistry of ruthenium porphyrin complexes." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/30790.

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This thesis work reports developments in the coordination chemistry of ruthenium porphyrin complexes, both in terms of the synthesis and chemistry of new compounds, as well as the study of the solution chemistry of some previously reported complexes. The synthesis, characterization and chemistry of ten new Ru(porp) coordination complexes in the oxidation states Ru[superscript]Ⅲ and Ru[superscript]Ⅳ containing halide (Br, CI) and other axial ligands (pyridine, CH₃CN, NH₃ and SbF₆) are described in this thesis. Some additional ten Ru(porp) complexes have been studied in situ. Measurement of the

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5

楊申鳴 and San-ming Yang. "Synthesis and characterization of some organoruthenium complexes containing 1,4,7-trimethyl-1,4,7-triazacyclononane." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1997. http://hub.hku.hk/bib/B42574699.

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6

Wong, Kwok-ming, and 黃國明. "Ruthenium-nitrogen and ruthenium-phosphorus multiple bonds supported by phthalocyanines: syntheses, spectroscopicproperties, and reactivities." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B45545893.

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Park, Sunghan. "Planar chiral arene ruthenium complexes." Thesis, Canberra, ACT : The Australian National University, 1993. http://hdl.handle.net/1885/140056.

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8

Yau, Benita Chui Kam. "Organometallic chemistry of phosphine complexes of iron and ruthenium." Thesis, The University of Sydney, 1992. https://hdl.handle.net/2123/26717.

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This thesis describes two projects involving the organometallic chemistry of iron and ruthenium complexes with DMPE ligands [DMPE = 1,2-bis(dimethylphosphino)ethane]. The first study involves an investigation into the kinetics and mechanisms of OH bond activation reactions of [Fe(DMPE)2]. The second project involves an investigation into the synthesis of RuH2(DMPE)2, the formation and properties of trans-[RuH(n2-H2)(DMPE)2]*, and the reactions of RuH2(DMPE)2 with alkyl and aryl thiols. In Part I of this work, the kinetics of the cis/trans isomerization of FeH(C6H5)(DMPE)2 and FeD(C6D5)(DMPE

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Williams, Michael Lloyd. "New aspects of organometallic chemistry /." Title page, contents and abstract only, 1985. http://web4.library.adelaide.edu.au/theses/09PH/09phw725.pdf.

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10

Rajapakse, Nimal. "Oxidations using dioxoruthenium (VI)-porphyrin complexes ; and studies on some organoruthenium-porphyrin species." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/30767.

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The oxidation of three alkyl thioethers, phenol and 2-propanol by trans-dioxo ruthenium porphyrin species, and the synthesis, characterization and reactivity of several new ruthenium porphyrin complexes are described in this thesis. The trans-dioxo species Ru(Porp)(O)₂ [Porp= the dianions of 5,10,15,20-tetramesitylporphyrin (TMP) and 5,10,15,20-(2,6-dichlorophenyl)porphyrin (OCP)] selectively oxidize diethyl-, di-n-butyl- and decylmethyl- sulfides to the corresponding sulfoxides at room temperature. The reaction is first order in [Ru] and in [thioether]. The second order rate constants for th

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Books on the topic "Organoruthenium compounds"

1

1937-, Murahashi Shunʾichi, ed. Ruthenium in organic synthesis. Weinheim: Wiley-VCH, 2004.

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2

1934-, Knox G. R., ed. Organometallic compounds of ruthenium and osmium. London: Chapman and Hall, 1985.

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3

Murahashi, Shun-Ichi. Ruthenium in Organic Synthesis. Wiley & Sons, Limited, John, 2005.

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4

Murahashi, Shun-Ichi. Ruthenium in Organic Synthesis. Wiley-VCH, 2004.

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Murahashi, Shun-Ichi. Ruthenium in Organic Synthesis. Wiley & Sons, Incorporated, John, 2006.

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