Статті в журналах з теми "Selenone"
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Abdel-Hafez, Shams H., Ragaa A. Ahmed, Mohamed A. Abdel-Azim, and Khairy M. Hassan. "Selenium containing Heterocycles: Part 1. Synthesis of Some New Substituted Pyrido[3′,2′:4,5]selenolo[3,2-d]pyrimidines and Related Fused Tetracyclic Systems." Journal of Chemical Research 2007, no. 10 (October 2007): 580–84. http://dx.doi.org/10.3184/030823407x25506.
Повний текст джерелаKorona-Głowniak, Izabela, Wojciech Nitek, Waldemar Tejchman, and Ewa Żesławska. "Influence of chlorine and methyl substituents and their position on the antimicrobial activities and crystal structures of 4-methyl-1,6-diphenylpyrimidine-2(1H)-selenone derivatives." Acta Crystallographica Section C Structural Chemistry 77, no. 10 (September 28, 2021): 649–58. http://dx.doi.org/10.1107/s205322962100975x.
Повний текст джерелаSarret, Géraldine, Laure Avoscan, Marie Carrière, Richard Collins, Nicolas Geoffroy, Francine Carrot, Jacques Covès, and Barbara Gouget. "Chemical Forms of Selenium in the Metal-Resistant Bacterium Ralstonia metallidurans CH34 Exposed to Selenite and Selenate." Applied and Environmental Microbiology 71, no. 5 (May 2005): 2331–37. http://dx.doi.org/10.1128/aem.71.5.2331-2337.2005.
Повний текст джерелаWazeer, Mohamed I. M., Anvarhusein A. Isab, and Ali El-Rayyes. "Solid state NMR study of 1,3imidazolidine-2-thione, 1,3-imidazolidine-2-selenone and some of their N-substituted derivatives." Spectroscopy 18, no. 1 (2004): 113–19. http://dx.doi.org/10.1155/2004/309130.
Повний текст джерелаHoier, H., H. L. Carrell, J. P. Glusker, and C. P. Spears. "Structure of ethyl phenyl selenone." Acta Crystallographica Section C Crystal Structure Communications 49, no. 3 (March 15, 1993): 520–23. http://dx.doi.org/10.1107/s0108270192008230.
Повний текст джерелаRostkowska, Hanna, Leszek Lapinski, Artem Khvorostov, and Maciej J. Nowak. "Proton transfer processes in selenourea: UV-induced selenone→selenol photoreaction and ground state selenol→selenone proton tunneling." Chemical Physics 298, no. 1-3 (March 2004): 223–32. http://dx.doi.org/10.1016/j.chemphys.2003.11.024.
Повний текст джерелаAltoum, Ali Osman S., Ali Alhoshani, Khalid Alhosaini, Muhammad Altaf, Saeed Ahmad, Saheed A. Popoola, Abdulaziz A. Al-Saadi, Adam A. Sulaiman, and Anvarhusein A. Isab. "Synthesis, characterization and in vitro cytotoxicity of platinum(II) complexes of selenones [Pt(selenone)2Cl2]." Journal of Coordination Chemistry 70, no. 6 (February 13, 2017): 1020–31. http://dx.doi.org/10.1080/00958972.2017.1287355.
Повний текст джерелаAnderson, Kim A., and Brandon Isaacs. "Determination of Selenium in Feeds, Premixes, Supplements, and Injectable Solutions by Hydride-Generated Inductively Coupled Plasma Atomic Emission Spectrometry." Journal of AOAC INTERNATIONAL 76, no. 4 (July 1, 1993): 910–13. http://dx.doi.org/10.1093/jaoac/76.4.910.
Повний текст джерелаHOIER, H., H. L. CARRELL, J. P. GLUSKER, and C. P. SPEARS. "ChemInform Abstract: Structure of Ethyl Phenyl Selenone." ChemInform 24, no. 27 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199327052.
Повний текст джерелаTian, Fengshou, Yahong Chen, Xiaofang Wang, Peng Li, and Shiwei Lu. "Oxidative Carbonylation of Aromatic Amines with CO Catalyzed by 1,3-Dialkylimidazole-2-selenone in Ionic Liquids." Journal of Chemistry 2015 (2015): 1–5. http://dx.doi.org/10.1155/2015/210806.
Повний текст джерелаŠibor, Jiří, Dalimil Žůrek, Radek Marek, Michal Kutý, Otakar Humpa, Jaromír Marek, and Pavel Pazdera. "2-(3-Acylselenoureido)benzonitriles and 2-(3-Acylselenoureido)thiophene-3-carbonitriles. Preparation, Structure Elucidation, Cyclization and Retrocyclization Reactions." Collection of Czechoslovak Chemical Communications 64, no. 10 (1999): 1673–95. http://dx.doi.org/10.1135/cccc19991673.
Повний текст джерелаAydin, A., H. Soylu, H. Kügükbay, Μ. Akkurt, and F. Ercan. "Crystal structure of 1,3-dimethylbenzimidazole-2-selenone, C9H10N2Se." Zeitschrift für Kristallographie - New Crystal Structures 214, no. 2 (June 1, 1999): 295–96. http://dx.doi.org/10.1515/ncrs-1999-0273.
Повний текст джерелаNajafi Chermhini, Alireza, Mostafa Abedi, Hossein Farrokhpour, Abbas Teimouri, and Bahareh Reisi. "Theoretical studies on the tautomerism of tetrazole selenone." Journal of Molecular Modeling 19, no. 10 (August 4, 2013): 4377–86. http://dx.doi.org/10.1007/s00894-013-1941-6.
Повний текст джерелаChermhini, Alireza Najafi, Hossein Farrokhpour, Abbas Teimouri, and Fatemah Pourmoghaddas. "Theoretical studies on tautomerism of imidazole-2-selenone." Structural Chemistry 24, no. 4 (October 25, 2012): 1215–27. http://dx.doi.org/10.1007/s11224-012-0153-5.
Повний текст джерелаIsab, Anvarhusein A., Saeed Ahmad, and Waqar Ashraf. "13C-n.m.r. studies of the binding of 1,3-diazinane-2-selenone and 1,3-diazipine-2-selenone to gold(I) drugs." Transition Metal Chemistry 30, no. 4 (May 2005): 389–92. http://dx.doi.org/10.1007/s11243-004-6966-3.
Повний текст джерелаNaz, Nimra, Saima Saqib, Rizwan Ashraf, Muhammad Irfan Majeed, and Muhammad Adnan Iqbal. "Synthesis of New Organoselenium Compounds: Characterization and Biological Studies." Macedonian Journal of Chemistry and Chemical Engineering 39, no. 1 (May 30, 2020): 1. http://dx.doi.org/10.20450/mjcce.2020.1912.
Повний текст джерелаCooper, Matthew A., and A. David Ward. "Synthesis and Substitution Reactions of N-Protected 2-(Phenylselenonylmethyl)pyrrolidines." Australian Journal of Chemistry 50, no. 3 (1997): 181. http://dx.doi.org/10.1071/c96148.
Повний текст джерелаZhang, Limin, and Thomas G. Chasteen. "Amending cultures of selenium-resistant bacteria with dimethyl selenone." Applied Organometallic Chemistry 8, no. 6 (October 1994): 501–8. http://dx.doi.org/10.1002/aoc.590080602.
Повний текст джерелаSwearingen, J. W., D. E. Fuentes, M. A. Araya, M. F. Plishker, C. P. Saavedra, T. G. Chasteen, and C. C. Vásquez. "Expression of the ubiE Gene of Geobacillus stearothermophilus V in Escherichia coli K-12 Mediates the Evolution of Selenium Compounds into the Headspace of Selenite- and Selenate-Amended Cultures." Applied and Environmental Microbiology 72, no. 1 (January 2006): 963–67. http://dx.doi.org/10.1128/aem.72.1.963-967.2006.
Повний текст джерелаAbduali, Baeshov, Ivanov Nikolay, and Myrzabekov Begzat. "Electrochemical Behavior of Selenium as Part of Composite Electrode in Sulfuric Acid Medium." JOURNAL OF ADVANCES IN CHEMISTRY 7, no. 3 (December 17, 2011): 1378–84. http://dx.doi.org/10.24297/jac.v7i3.2373.
Повний текст джерелаŻesławska, Ewa, Izabela Korona-Głowniak, Wojciech Nitek, and Waldemar Tejchman. "Effect of the position of a methoxy substituent on the antimicrobial activity and crystal structures of 4-methyl-1,6-diphenylpyrimidine-2(1H)-selenone derivatives." Acta Crystallographica Section C Structural Chemistry 76, no. 4 (March 31, 2020): 359–66. http://dx.doi.org/10.1107/s2053229620004040.
Повний текст джерелаTanino, Keiji, Jun-ichiro Kishi, Kazutada Ikeuchi, and Takahiro Suzuki. "Synthetic Studies of Daphniphyllum Alkaloids: A New Method for the Construction of [7-5-5] All-Carbon Tricyclic Skeleton." Synlett 33, no. 02 (October 29, 2021): 196–200. http://dx.doi.org/10.1055/a-1682-9415.
Повний текст джерелаAVOSCAN, L., H. KHODJA, M. CARRIÈRE, J. COVÈS, and B. GOUGET. "PIXE ANALYSES OF THE SOLUBLE AND MEMBRANE SE-CONTAINING PROTEINS EXTRACTED FROMCUPRIAVIDUS METALLIDURANSCH34 AFTER SELENIUM OXIDES CHALLENGE." International Journal of PIXE 18, no. 03n04 (January 2008): 91–99. http://dx.doi.org/10.1142/s0129083508001430.
Повний текст джерелаŻesławska, Ewa, Izabela Korona-Głowniak, Małgorzata Szczesio, Andrzej Olczak, Alicja Żylewska, Waldemar Tejchman, and Anna Malm. "Structural analysis and antimicrobial activity of 2[1H]-pyrimidinethione/selenone derivatives." Journal of Molecular Structure 1142 (August 2017): 261–66. http://dx.doi.org/10.1016/j.molstruc.2017.04.067.
Повний текст джерелаWazeer, Mohammed I. M., and Anvarhusein A. Isab. "Solution and solid-state NMR studies of some cadmium–selenone complexes." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 62, no. 4-5 (December 2005): 880–85. http://dx.doi.org/10.1016/j.saa.2005.03.020.
Повний текст джерелаNesterov, V. N., V. E. Shklover, Yu T. Struchkov, V. P. Litvinov, E. �. Apenova, V. Yu Mortikov, and Yu A. Sharanin. "Crystal structure of 6-(1-adamantyl)-3-cyanopyridine-2(1H)-selenone." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, no. 2 (February 1988): 397–99. http://dx.doi.org/10.1007/bf00957459.
Повний текст джерелаChasteen, Thomas G. "Confusion between dimethyl selenenyl sulfide and dimethyl selenone released by bacteria." Applied Organometallic Chemistry 7, no. 5 (September 1993): 335–42. http://dx.doi.org/10.1002/aoc.590070507.
Повний текст джерелаHughes, David, Tereza Kunická, Lutz Schomburg, Václav Liška, Niall Swan, and Pavel Souček. "Expression of Selenoprotein Genes and Association with Selenium Status in Colorectal Adenoma and Colorectal Cancer." Nutrients 10, no. 11 (November 21, 2018): 1812. http://dx.doi.org/10.3390/nu10111812.
Повний текст джерелаPalomba, M., L. Rossi, L. Sancineto, E. Tramontano, A. Corona, L. Bagnoli, C. Santi, C. Pannecouque, O. Tabarrini, and F. Marini. "A new vinyl selenone-based domino approach to spirocyclopropyl oxindoles endowed with anti-HIV RT activity." Organic & Biomolecular Chemistry 14, no. 6 (2016): 2015–24. http://dx.doi.org/10.1039/c5ob02451j.
Повний текст джерелаBosse, Astrid C., Josef Pallauf, Bettina Hommel, Mariana Sturm, Susanne Fischer, Nicole M. Wolf, and Andreas S. Mueller. "Impact of selenite and selenate on differentially expressed genes in rat liver examined by microarray analysis." Bioscience Reports 30, no. 5 (April 9, 2010): 293–306. http://dx.doi.org/10.1042/bsr20090089.
Повний текст джерелаCemeli, Eduard, Ricard Marcos, and Diana Anderson. "Genotoxic and antigenotoxic properties of selenium compounds in thein vitromicronucleus assay with human whole blood lymphocytes and tk6 lymphoblastoid cells." Scientific World JOURNAL 6 (2006): 1202–10. http://dx.doi.org/10.1100/tsw.2006.204.
Повний текст джерелаAlhoshani, Ali, Adam A. A. Seliman, Ali Osman Altoum, Hatem A. Abuelizz, Saeed Ahmad, Muhammad Altaf, Khalid H. Omer, Manzar Sohail, and Anvarhusein A. Isab. "Synthesis, X-ray structure and in vitro cytotoxicity of trans-diammineplatinum(II) complexes of selenones, trans-[Pt(NH3)2(selenone)2](NO3)2." Polyhedron 158 (January 2019): 234–40. http://dx.doi.org/10.1016/j.poly.2018.09.010.
Повний текст джерелаFerreira, Gabriela de Sousa, Paulo Ovidio Batista de Brito, Tiago de Abreu Lima, Francisco Ícaro Carvalho Aderaldo, Gabrielli Teles de Carvalho, Elias do Nascimento de Sousa Filho, and Franklin Aragão Gondim. "Plant Growth and Antioxidative Enzymes in Sunflower Supplemented With Selenium." Journal of Agricultural Science 15, no. 1 (December 15, 2022): 62. http://dx.doi.org/10.5539/jas.v15n1p62.
Повний текст джерелаGolob, Aleksandra, Katarina Vogel-Mikuš, Nina Brudar, and Mateja Germ. "Duckweed (Lemna minor L.) Successfully Accumulates Selenium from Selenium-Impacted Water." Sustainability 13, no. 23 (December 3, 2021): 13423. http://dx.doi.org/10.3390/su132313423.
Повний текст джерелаOnoguchi, Aina, Giuseppe Granata, Daisuke Haraguchi, Hiroshi Hayashi, and Chiharu Tokoro. "Kinetics and mechanism of selenate and selenite removal in solution by green rust-sulfate." Royal Society Open Science 6, no. 4 (April 2019): 182147. http://dx.doi.org/10.1098/rsos.182147.
Повний текст джерелаFrolov, K. A., V. V. Dotsenko, S. G. Krivokolysko, and V. P. Litvinov. "Synthesis of derivatives of 3,5,7,11-tetraaza-tricyclo[7.3.1.02,7]tridec-2-ene-8-selenone." Chemistry of Heterocyclic Compounds 46, no. 9 (December 2010): 1142–43. http://dx.doi.org/10.1007/s10593-010-0641-8.
Повний текст джерелаWazeer, Mohamed I. M., Anvarhusein A. Isab, and Herman P. Perzanowski. "Solid-state NMR studies of 1,3-imidazolidine-2-selenone and some related compounds." Magnetic Resonance in Chemistry 41, no. 12 (2003): 1026–29. http://dx.doi.org/10.1002/mrc.1305.
Повний текст джерелаYu, Rui, John P. Coffman, Verena van Fleet-Stalder, and Thomas G. Chasteen. "Toxicity of oxyanions of selenium and of a proposed bioremediation intermediate, dimethyl selenone." Environmental Toxicology and Chemistry 16, no. 2 (February 1997): 140–45. http://dx.doi.org/10.1002/etc.5620160207.
Повний текст джерелаPoluboyarinov, P. A., D. G. Elistratov, and V. I. Shvets. "METABOLISM AND MECHANISM OF TOXICITY OF SELENIUM-CONTAINING SUPPLEMENTS USED FOR OPTIMIZING HUMAN SELENIUM STATUS." Fine Chemical Technologies 14, no. 1 (February 28, 2019): 5–24. http://dx.doi.org/10.32362/2410-6593-2019-14-1-5-24.
Повний текст джерелаGUPTA, UMESH C., and K. A. WINTER. "EFFECT OF SELENATE VS. SELENITE FORMS OF SELENIUM IN INCREASING THE SELENIUM CONCENTRATION IN FORAGES AND CEREALS." Canadian Journal of Soil Science 69, no. 4 (November 1, 1989): 885–88. http://dx.doi.org/10.4141/cjss89-090.
Повний текст джерелаHolschumacher, Dirk, Constantin G. Daniliuc, Peter G. Jones, and Matthias Tamm. "Sulfur and SeleniumActivation by Frustrated NHC/B(C6F5)3 Lewis Pairs; Conformational Flexibility of Products." Zeitschrift für Naturforschung B 66, no. 4 (April 1, 2011): 371–77. http://dx.doi.org/10.1515/znb-2011-0406.
Повний текст джерелаMohapatra, Dipti Prakash, Kelly Ann Robinson, Fang Huang, Deepak Kirpalani, and Michele Christine Loewen. "Insights into Increasing Selenate Reductase Enzyme Activity in the Presence of Nitrogen-Doped Graphite Electrodes for Selenium Effluent Treatment." Water 14, no. 6 (March 16, 2022): 931. http://dx.doi.org/10.3390/w14060931.
Повний текст джерелаAYGÜN, Muhittin, Engin ÇETINKAYA, Yetkin GÖK, Engin KENDI, and Bekir ÇETINKAYA. "Synthesis and Crystal Structure of Hexahydrobis[(1,3-p-dimethylaminobenzyl)-1,3-diazepine]-2-selenone, C23H32N4Se." Analytical Sciences 19, no. 7 (2003): 1093–94. http://dx.doi.org/10.2116/analsci.19.1093.
Повний текст джерелаElsabawy, Khaled M., and Shams H. Abdel-Hafez. "Molecular structural visualization and micro-structural features of 4,6-dimethyl-3-cyanopyridine-(2H)-selenone." Materials Chemistry and Physics 132, no. 2-3 (February 2012): 631–36. http://dx.doi.org/10.1016/j.matchemphys.2011.11.079.
Повний текст джерелаElambalassery, J. G., and S. Sreedevi. "Qualitative and Quantitative Study on Internal Rotation During Tautomerization of Thione, Selenone, and Tellurone." Journal of Structural Chemistry 59, no. 7 (December 2018): 1534–43. http://dx.doi.org/10.1134/s0022476618070041.
Повний текст джерелаZhu, Huajian, Honghao Sun, Yang Liu, Yiping Duan, Jie Liu, Xue Yang, Wenlong Li, et al. "Design, synthesis and biological evaluation of vinyl selenone derivatives as novel microtubule polymerization inhibitors." European Journal of Medicinal Chemistry 207 (December 2020): 112716. http://dx.doi.org/10.1016/j.ejmech.2020.112716.
Повний текст джерелаChristensen, M. K., C. J. Frederickson, and G. Danscher. "Retrograde tracing of zinc-containing neurons by selenide ions: a survey of seven selenium compounds." Journal of Histochemistry & Cytochemistry 40, no. 4 (April 1992): 575–79. http://dx.doi.org/10.1177/40.4.1313065.
Повний текст джерелаHao, Wenbin, Chunmei Tao, Tanveer M. Adyel, Junjie Zhao, Jun Hou, Lingzhan Miao, and Yuan Zeng. "Effects of Selenium in Different Valences on the Community Structure and Microbial Functions of Biofilms." Water 14, no. 15 (August 2, 2022): 2394. http://dx.doi.org/10.3390/w14152394.
Повний текст джерелаRen, Bingyu, Yanmei Huang, Chen Zou, Yingying Wu, Yuru Huang, Jiazuan Ni, and Jing Tian. "Transcriptional Regulation of Selenoprotein F by Heat Shock Factor 1 during Selenium Supplementation and Stress Response." Cells 8, no. 5 (May 18, 2019): 479. http://dx.doi.org/10.3390/cells8050479.
Повний текст джерелаRodrigo, S., O. Santamaría, López-Bellido FJ, and Poblaciones MJ. "Agronomic selenium biofortification of two-rowed barley under Mediterranean conditions ." Plant, Soil and Environment 59, No. 3 (January 19, 2013): 115–20. http://dx.doi.org/10.17221/691/2012-pse.
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