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Journal articles on the topic 'Novel organotellurium compound'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Lima, Camila Bárbara Cantalupo, Wagner Welber Arrais-Silva, Rodrigo Luiz Oliveira Rodrigues Cunha, and Selma Giorgio. "A Novel Organotellurium Compound (RT-01) as a New Antileishmanial Agent." Korean Journal of Parasitology 47, no. 3 (2009): 213. http://dx.doi.org/10.3347/kjp.2009.47.3.213.

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2

Sailer, Brian, Nathan Liles, Sarah Dickerson, and Thomas Chasteen. "Cytometric determination of novel organotellurium compound toxicity in a promyelocytic (HL-60) cell line." Archives of Toxicology 77, no. 1 (2003): 30–36. http://dx.doi.org/10.1007/s00204-002-0407-x.

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3

Vázquez-Tato, M., Alberto Mena-Menéndez, Xesús Feás, and Julio Seijas. "Novel Microwave-Assisted Synthesis of the Immunomodulator Organotellurium Compound Ammonium Trichloro(dioxoethylene-O,O')tellurate (AS101)." International Journal of Molecular Sciences 15, no. 2 (2014): 3287–98. http://dx.doi.org/10.3390/ijms15023287.

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4

Yasuike, Shuji, Masanobu Uchiyama, Mio Matsumura, et al. "Synthesis and Structural Characterization of a Novel Organotellurium Compound: Dinaphtho[2,3-b;2’,3’-d]tellurophene." HETEROCYCLES 90, no. 1 (2015): 121. http://dx.doi.org/10.3987/com-14-s(k)30.

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5

Abondanza, T. S., C. R. Oliveira, C. M. V. Barbosa, et al. "Bcl-2 expression and apoptosis induction in human HL60 leukaemic cells treated with a novel organotellurium(IV) compound RT-04." Food and Chemical Toxicology 46, no. 7 (2008): 2540–45. http://dx.doi.org/10.1016/j.fct.2008.04.010.

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6

Yosef, Sigal, Miri Brodsky, Benjamin Sredni, Amnon Albeck, and Michael Albeck. "Octa-O-bis-(R,R)-Tartarate Ditellurane (SAS)—a Novel Bioactive Organotellurium(IV) Compound: Synthesis, Characterization, and Protease Inhibitory Activity." ChemMedChem 2, no. 11 (2007): 1601–6. http://dx.doi.org/10.1002/cmdc.200700155.

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7

Sies, Helmut, Lars-Oliver Klotz, Victor S. Sharov, Annika Assmann, and Karlis Briviba. "Protection against Peroxynitrite by Selenoproteins." Zeitschrift für Naturforschung C 53, no. 3-4 (1998): 228–32. http://dx.doi.org/10.1515/znc-1998-3-412.

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Abstract Cellular defense against excessive peroxynitrite generation is required to protect against DNA strand-breaks and mutations and against interference with protein tyrosine-based sig naling and other protein functions due to formation of 3-nitrotyrosine. We recently demon strated a role of selenium-containing enzymes catalyzing peroxynitrite reduction. Glutathione peroxidase (GPx) protected against the oxidation of dihydrorhodamine 123 (D H R) by perox ynitrite more effectively than ebselen (2-phenyl-1,2-benzisoselenazol-3(2H)-one), a selenoor-ganic compound exhibiting a high second-o

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8

Dhir, Rupy, and Jaspreet Dhau. "Synthesis and antioxidant ability of novel tellurium assisted unusual coordination number copper complex of pyridine based organotellurium compound: Single crystal X-ray structure of ligand and metal complex." Journal of Organometallic Chemistry 1006 (February 2024): 123021. http://dx.doi.org/10.1016/j.jorganchem.2024.123021.

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9

Engman, Lars, and Vijay Gupta. "Novel group transfer cyclization reactions of organotellurium compounds." Journal of the Chemical Society, Chemical Communications, no. 24 (1995): 2515. http://dx.doi.org/10.1039/c39950002515.

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10

Mihoya, Aya, Shinichi Koguchi, Yuga Shibuya, Minato Mimura, and Makoto Oba. "Oxidation of Thiol Using Ionic Liquid-Supported Organotelluride as a Recyclable Catalyst." Catalysts 10, no. 4 (2020): 398. http://dx.doi.org/10.3390/catal10040398.

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Organotellurium compounds are known to be useful oxidation reagents. For developing a recoverable and reusable reagent, this paper describes the use of an ionic liquid (IL) support for the organotellurium reagent and its application as a recyclable catalyst for thiol oxidation. We have successfully prepared a novel diphenyl telluride derivative 5 bearing an imidazolium hexafluorophosphate group in its structure. It is found that the IL-supported diphenyl telluride 5 efficiently catalyzed the aerobic oxidation of various thiols in [bmim]PF6 solution under photosensitized conditions to provide t

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11

Y., D. KULKARNI, RANI ARCHNA та A. SIDDIQUI R. "Synthesis of some New α,α'-Bis(3-nitro/aminobenzoyl)tellurium Dichlorides : A Search for Biologically Active Organotellurium Compounds". Journal of Indian Chemical Society Vol. 69, Jul 1992 (1992): 353–55. https://doi.org/10.5281/zenodo.6003643.

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Department of Chemistry, Lucknow University, Lucknow-226 007 I. T. R. C., Lucknow-226 007 <em>Manuscript received 30 December 1991, revised 6 May 1992, accepted 15 May 1992</em> Novel α ,α'-bis(3-nitro/amino)benzoyltellurium dichlorides, their adducts with nitrogen donor molecules have been synthesised The effect of these compounds on the levels of enzyme (Acetylcholine hydrolase) activity was studied against albino mice.

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12

ENGMAN, L., and V. GUPTA. "ChemInform Abstract: Novel Group Transfer Cyclization Reactions of Organotellurium Compounds." ChemInform 27, no. 20 (2010): no. http://dx.doi.org/10.1002/chin.199620058.

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13

Dabdoub, Miguel J., Vânia B. Dabdoub, and Joseph P. Marino. "Novel and general cross-coupling reactions of alkynylzinc reagents and organotellurium compounds." Tetrahedron Letters 41, no. 4 (2000): 437–40. http://dx.doi.org/10.1016/s0040-4039(99)02088-2.

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14

Patel, Jayna A., Aundrea M. Lee, Donna V. Franklin, Frank R. Fronczek та Thomas Junk. "Cyclization Reactions Involving 2-Aminoarenetellurols and Derivatives of α,β-Unsaturated Carboxylic Acids". Heteroatom Chemistry 2021 (22 грудня 2021): 1–8. http://dx.doi.org/10.1155/2021/7140222.

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The reductive cyclization of arenetellurols carrying α,β-unsaturated amide functionalities in the ortho position was investigated. Conceptually, such compounds can form 1,3-tellurazoles without the involvement of the unsaturation in the ring closure, they can form 1,4-tellurazinone derivatives, or they can undergo ring closure to 1,5-tellurazepinones. Amides derived from acrylic and methacrylic acid generated 1,5-tellurazepinones while 2-cinnamylamidobenzenetellurol cyclized to a 1,3-tellurazole derivative. In contrast, the reaction of acetylenedicarboxylic acid and its derivatives with 2-amin

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15

Wang, Lei, and Zhizhen Huang. "First Application of Ionic Liquid to Reactions Involving Organotellurium Compounds as Intermediates." Journal of Chemical Research 2005, no. 7 (2005): 446–48. http://dx.doi.org/10.3184/030823405774309069.

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The condensation reaction of telluronium salts 1 with aldehydes and dibutyl telluride 4, bromide 5 with aldehyde 2 proceeded smoothly in the ionic solvent [bmim][BF4], affording a novel method for the stereoselective synthesis of (E)-α,β-unsaturated compounds 3 in high purity, excellent yields and high stereoselectivity.

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16

Dabdoub, Miguel J., Vania B. Dabdoub, and Joseph P. Marino. "ChemInform Abstract: Novel and General Cross-Coupling Reactions of Alkynylzinc Reagents and Organotellurium Compounds." ChemInform 31, no. 17 (2010): no. http://dx.doi.org/10.1002/chin.200017070.

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17

Songlin, Zhang, Zhang Yongmin, and Li Qiaoling. "Sm/ZrCl4 induced reductive cleavage of Te-Te bond in diaryl ditellurides : A novel method for the synthesis of unsymmetrical tellurides." Journal of Indian Chemical Society Vol. 78, Mar 2001 (2001): 144–45. https://doi.org/10.5281/zenodo.5872875.

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Department of Chemistry, Zhejiang University at Xi Xi Campus, Hangzhou, 310028, P. R. China <em>Manuscript received 12 July 1999, accepted 20 September 1999</em> Diaryl ditellurides are reduced by the system of Sm/ZrCI<sub>4</sub><strong> </strong>to produce samarium aryltellurolates which react with alkyl halides to afford tellurides.

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18

Potapov, Vladimir A., Svetlana V. Amosova, and Valentina Yu Shestakova. "Novel Synthesis of Unsaturated Organoselenium and Organotellurium Compounds Based on Organic Dichalcogenides and Elemental Chalcogens." Phosphorus, Sulfur, and Silicon and the Related Elements 136, no. 1 (1998): 205–8. http://dx.doi.org/10.1080/10426509808545944.

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19

Miyasato, Masataka, Mao Minoura, Yohsuke Yamamoto, and Kin-ya Akiba. "Novel Valence Expansion Reactions Using KC8: A New Route to Hexavalent Organotellurium Compounds from Divalent Tellurium." Chemistry Letters 31, no. 3 (2002): 288–89. http://dx.doi.org/10.1246/cl.2002.288.

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20

Sailer, Brian L., Tarl Prow, Sarah Dickerson, et al. "Bacterial cytotoxicity and induction of apoptosis in promyelocytic (Line HL-60) cells by novel organotellurium compounds." Environmental Toxicology and Chemistry 18, no. 12 (1999): 2926–33. http://dx.doi.org/10.1002/etc.5620181239.

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21

Cunha, Rodrigo L. O. R., Miriam E. Urano, Jair R. Chagas, et al. "Tellurium-based cysteine protease inhibitors: evaluation of novel organotellurium(IV) compounds as inhibitors of human cathepsin B." Bioorganic & Medicinal Chemistry Letters 15, no. 3 (2005): 755–60. http://dx.doi.org/10.1016/j.bmcl.2004.11.012.

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22

Potapov, Vladimir A., Svetlana V. Amosova, and Valentina Yu Shestakova. "ChemInform Abstract: Novel Synthesis of Unsaturated Organoselenium and Organotellurium Compounds Based on Organic Dichalcogenides and Elemental Chalcogens." ChemInform 31, no. 28 (2010): no. http://dx.doi.org/10.1002/chin.200028268.

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23

Yamago, Shigeru, Kazunori Iida, and Jun-ichi Yoshida. "Organotellurium Compounds as Novel Initiators for Controlled/Living Radical Polymerizations. Synthesis of Functionalized Polystyrenes and End-Group Modifications." Journal of the American Chemical Society 124, no. 12 (2002): 2874–75. http://dx.doi.org/10.1021/ja025554b.

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24

Tucci, Amanda Resende, Raquel Mello da Rosa, Alice Santos Rosa, et al. "Antiviral Effect of 5′-Arylchalcogeno-3-aminothymidine Derivatives in SARS-CoV-2 Infection." Molecules 28, no. 18 (2023): 6696. http://dx.doi.org/10.3390/molecules28186696.

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The understanding that zidovudine (ZDV or azidothymidine, AZT) inhibits the RNA-dependent RNA polymerase (RdRp) of SARS-CoV-2 and that chalcogen atoms can increase the bioactivity and reduce the toxicity of AZT has directed our search for the discovery of novel potential anti-coronavirus compounds. Here, the antiviral activity of selenium and tellurium containing AZT derivatives in human type II pneumocytes cell model (Calu-3) and monkey kidney cells (Vero E6) infected with SARS-CoV-2, and their toxic effects on these cells, was evaluated. Cell viability analysis revealed that organoselenium (

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25

Haithem, J. Kadhum. "Bis4-(4́-hydroxy-3́-methoxy benzylidine aminophenyl) telluride prevents sodium nitrite induced changes in haematological parameters of adult's male rats." January 27, 2022. https://doi.org/10.5281/zenodo.5910650.

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<strong>Sodium nitrite (NaNO<sub>2</sub>) is highly toxic, flammable and a strong oxidant substance. It oxidizes hemoglobin into methemglobin. The aim from this study is to evaluate the role of the novel organotellurium compound [bis4-(4́-hydroxy-3́-methoxy benzylidine amino phenyl) telluride] in preventing sodium nitrite induced hematological changes in adult's male rats. Forty adults' male rats were used in this study; they were divided into 5 equal groups. The 1<sup>st</sup> group is control, the 2nd group was given 0.2% NaNO<sub>2</sub> in the drinking water, the 3<sup>rd</sup> and

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26

Reis de Sá, L. F., F. T. Toledo, A. C. Gonçalves, et al. "Synthetic Organotellurium Compounds Sensitize Drug-Resistant Candida albicans Clinical Isolates to Fluconazole." Antimicrobial Agents and Chemotherapy 61, no. 1 (2016). http://dx.doi.org/10.1128/aac.01231-16.

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ABSTRACT Invasive Candida albicans infections are a serious health threat for immunocompromised individuals. Fluconazole is most commonly used to treat these infections, but resistance due to the overexpression of multidrug efflux pumps is of grave concern. This study evaluated the ability of five synthetic organotellurium compounds to reverse the fluconazole resistance of C. albicans clinical isolates. Compounds 1 to 4, at <10 μg/ml, ameliorated the fluconazole resistance of Saccharomyces cerevisiae strains overexpressing the major C. albicans multidrug efflux pumps Cdr1p and Mdr1p, wherea

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27

Yosef, Sigal, Miri Brodsky, Benjamin Sredni, Amnon Albeck, and Michael Albeck. "ChemInform Abstract: Octa-O-bis-(R,R)-Tartarate Ditellurane (SAS) - A Novel Bioactive Organotellurium(IV) Compound: Synthesis, Characterization, and Protease Inhibitory Activity." ChemInform 39, no. 4 (2008). http://dx.doi.org/10.1002/chin.200804198.

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28

Zhou, Xue-Qi, Hai-Tao Tang, Fei-Hu Cui, Ying Liang, Shu-Hui Li, and Ying-Ming Pan. "Electrocatalytic three-component reactions: synthesis of tellurium containing oxazolidinone for anticancer agents." Green Chemistry, 2023. http://dx.doi.org/10.1039/d3gc01288c.

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Synthesis of organotellurium compounds are crucial in pharmaceutical science. Herein, a novel and efficient electrochemically catalyzed multicomponent reaction of propargylamide or propargylamine, CO2, and ditelluriumh has been developed and a...

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29

Tanini, Damiano, and Antonella Capperucci. "Tellurium-containing thiol-peroxidase-like antioxidants and their catalytic mechanism." Current Chemical Biology 17 (November 21, 2022). http://dx.doi.org/10.2174/2212796817666221121155138.

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Abstract: The development of novel small molecules with effective catalytic antioxidant properties is highly sought after. A wide array of structurally diverse selenium- and tellurium-containing glutathione peroxidase mimics have been studied over the past two decades. Within this arena, organotellurium compounds generally exhibit higher catalytic properties with respect to selenium-containing analogues. Different mechanisms accounting for the thiol-peroxidase-like activity of various classes of organotellurium derivatives have been proposed. This review document develops this area and provide

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30

Bhardwaj, Anisha, Manish Kumar, Sapana Garg, and Anjaneyulu Bendi. "Theoretical and Experimental In‐vitro Studies of Novel Thiophene Based Organotellurium(IV) Complexes." Chemistry & Biodiversity, January 2024. http://dx.doi.org/10.1002/cbdv.202301544.

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Schiff bases are one of the important classes of organic compounds containing imine or azomethine functional groups with potential biological applications in medicinal chemistry. These bases played a significant role in developing inorganic, bioinorganic, and optical materials and coordination complexes. Nowadays, these compounds have attracted the scientific community's attention due to their ability to act as ligands in the formation of stable metal complexes with significant biological activity. In this connection, we have designed and synthesized some novel thiophene‐based organoltellurium

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